ORTHOPEDIC MCQS ONLINE QUESTION BANK H1C

ORTHOPEDIC MCQS ONLINE QUESTION BANK H1C


Which of the following fractures occurs through a single application of force:
1) A minimally displaced femoral neck fracture in a long distance runner
3) A fifth rib fracture in a collegiate rower
2) A second metatarsal fracture in a Naval Academy midshipman
5) A proximal one-third posterior tibial cortex fracture in a long distance runner
4) A short spiral humerus fracture in a baseball catcher
The femoral neck fracture, metatarsal fracture, rib fracture, and the tibial fracture are stress fractures that result from repetitive loading.
In contrast, the humeral fracture in the baseball catcher is secondary to failure of the humerus secondary to a pure torsional force. Long bones are at their weakest when loaded in pure torsion.
Correct Answer: A short spiral humerus fracture in a baseball catcher

674. (872) Q2-1135:
Which of the following statements is true concerning the vascularity at a fracture site
:
1) Periosteal blood vessels are capable of supplying the endosteal region.
3) Reamed intramedullary rods do not significantly interrupt endosteal blood supply.
2) Fracture site blood flow peaks at 2 weeks.
5) In animal studies, blood flow is greater at 42 days in rodded vs. plated tibias.
4) In animal studies, blood flow is greater at 120 days in plated vs. rodded tibias.
In the normal long bone, the periosteal vessels supply the outer one-third of the cortex. The nutrient artery enters at the diaphysis of a long bone and has ascending and descending vessels that supply the inner two-thirds of the cortex.
Important points to remember:
The periosteal blood supply cannot supply the inner two-thirds of the cortex even if the endosteal blood supply has been interrupted, as in intramedullary reaming.
Blood flow markedly drops at the fracture site at the time of the fracture and peaks at 2 weeks.
Intramedullary reamed rods destroy the endosteal blood supply. In dog experiments, the blood supply is reconstituted to normal in 120 days.
In dog experiments, the blood supply is decreased in both plated and rodded tibias at 42 and 90 days. The decrease is greater in the rodded tibias.
The oxygen tension is low in the fracture hematoma and in the newly formed cartilage and bone. The oxygen tension is highest in the fibrous tissue. The hypoxic state favors cartilage formation.
6Correct Answer: Fracture site blood flow peaks at 2 weeks.

75. (873) Q2-1137:
Which of the following statements is true concerning molecular events at the site of a healing fracture:
1) Type II collagen production is lowest during the first 2 weeks.
3) Periosteal type III collagen serves as a substrate for migration of osteoprogenitor cells and capillary ingrowth.
2) Type I collagen production is highest during the first 2 weeks.
5) Types V and XI collagen control the maturation of mineralization crystals.
4) Type IX collagen initiates mineralization of type II collagen.
Important points to remember concerning molecular events at the fracture site:
Type II collagen production is highest during the first 2 weeks. Cartilage is the first tissue produced at the fracture site. The chondrocytes hypertrophy and release matrix vesicles that prepare the extracellular matrix for mineralization of the cartilage. Blood vessels grow into the hypertrophied cartilage cells and perivascular cells become osteoblasts and begin mineralization. This is the exact same process that occurs at the growth plate with formation of the primary and secondary spongiosa.
Type I collagen production is low during the first 2 weeks as cartilage is initially formed. Type I collagen production is highest as the cartilage is mineralized later.
Periosteal type III collagen serves as a substrate for the migration of osteoprogenitor cells and capillary ingrowth. Type IX collagen contributes to the mechanical stability of type II collagen.
Types V and XI collagen regulate the growth and orientation of types I and II collagen fibrils.
Correct Answer: Periosteal type III collagen serves as a substrate for migration of osteoprogenitor cells and capillary ingrowth.

 

676. (874) Q2-1138:
Which of the following statements is true concerning the molecular events involved in fracture healing:

1) Osteonectin plays a role in early ossification.
3) Osteopontin plays no role in normal bone remodeling.
2) Osteocalcin inhibits intramembranous bone formation.
5) Osteonectin is found in proliferating and hypertrophic chondrocytes rather than extracellular matrix.
4) Fibronectin inhibits cell migration and adhesion.
There are several noncollagenous proteins that are important in bone repair and regeneration:
Osteonectin â The gene for osteonectin is expressed at the onset of both intramembranous and enchondral ossification. It may play a role in the regulation of cell function in the early stages of ossification.
Osteocalcin â Osteocalcin is expressed in the fracture callus only by osteoblastic cells. This protein may have a role in intramembranous subperiosteal bone formation.
Osteopontin â This protein is found in the extracellular matrix and is important in cellular attachment. It is found in osteocytes and osteoprogenitor cells. Osteopontin may play a role in bone remodeling.
Fibronectin â This protein plays a role in early fracture healing and is found in the fracture hematoma within 3 days. Fibronectin mediates adhesion and migration. It is found in the fibrous portions of provisional matrices and in cartilage matrix. The potential role for this protein is the establishment of provisional fibers in cartilaginous matrices.
Correct Answer: Osteonectin plays a role in early ossification.
677. (933) Q2-1220:
Which of the following is not a clinical sign of rickets?

1) Irritability
3) Localized bone pain
2) Frontal bossing
5) Enlarged epiphyses
4) Short stature
Localized bone pain is not a common finding in rickets. In contrast, in osteomalacia, bone pain is very common. The features of rickets that one should remember include:
Apathy
Irritability
Short stature
Positive Gowers sign
Laxity
Frontal bossing
Rachitic rosary, Harrisonâs groove enlarged physes Correct Answer: Localized bone pain
1) Bone pain
3) Pathologic fractures
2) Brown tumors
5) Tetany
4) Renal stones
Features of primary hyperparathyroidism include bone pain, brown tumors, pathologic fractures, and kidney stones. Tetany is not a finding.
Here are some common features to remember: Common, incidence 1 in 500-1,000
Females (usually postmenopausal) greater than men, 3:1 Etiology
Benign, solitary adenoma (80%) Four gland parathyroid hyperplasia Parathyroid carcinoma (<0.5%)
Osteitis fibrosa cystica
Subperiosteal resorption of distal phalanx Tapering of distal clavicle
Bone cysts Brown tumors
Kidney stones
Peptic ulcer disease and pancreatitis Biochemical hallmarks
Hypercalcemia
Elevated PTH (phosphorus lower range of normal, 1/3 low) Neuromuscular syndrome
Easy fatigue, weakness, older than you seem
Bone mineral density - excellent marker of the disease - low in distal radius (cortical bone) and normal at vertebra (cancellous bone)
Treatment - neck exploration and removal of the parathyroid adenoma Correct Answer: Tetany
679. (935) Q2-1222:
Which of the following is the most likely origin for the greater medullary artery (Adamkiewicz artery):
1) Lower cervical segmental
3) Middle thoracic segmental
2) Upper thoracic segmental
5) Upper lumbar segmental
4) Lower thoracic segmental
The major part of the blood supply of the spinal cord is provided by the medullary or radicular arteries. The only feeder for the lower thoracic spine cord is the greater medullary artery or artery of Adamkiewicz (T9-T11).
One should remember that in the thoracic spine the right-sided approach is preferred to avoid the aorta and segmental artery of Adamkiewicz.
Correct Answer: Lower thoracic segmental
1) The anterior humeral circumflex artery
3) The posterior humeral circumflex artery
2) Axillary artery
5) Subscapular artery
4) Acromial branch of thoracoacromial artery
The humeral head has been shown to be perfused primarily by the anterolateral ascending branch of the anterior circumflex artery. This branch runs parallel to the lateral aspect of the tendon of the long head of the biceps and enters the humeral head where the proximal end of the intertubercular groove meets the greater tuberosity. The posterior circumflex artery provides only the posterior portion of the greater tuberosity and a small posteroinferior part of the head.Correct Answer: The anterior humeral circumflex artery
681. (937) Q2-1225:
A 4-year-old child injures his elbow and presents with swelling and limitation of voluntary movement. The radiographs show no obvious fracture, but it does show a Baumann angle of 71° and an elevation of the posterior fat pad. You tell the parents that this most likely represents:
1) A congenital anomaly with a valgus deformity of the elbow
3) A Salter I physeal separation
2) A medial epicondyle fracture
5) A variation of normal
4) An occult supracondylar fracture
Occult supracondylar fracture was the most common diagnosis assigned after careful study of a clinical series of elevated pediatric posterior fat pads.
The value for Baumann angle is normally 73° ± 6°. Nothing in this description suggests a congenital anomaly. Medial epicondyle fractures are extremely rare before 9 years of age.
Although a Salter I physeal separation is a possibility, it is a rare injury.
With an elevation of the posterior fat pad, there is increasing recognition that a fracture exists.
Correct Answer: An occult supracondylar fracture
682. (1049) Q2-1356:
The tibialis anterior muscle is principally innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The tibialis anterior muscle is primarily innervated by the L4 nerve root. The tibialis anterior muscle also receives innervation from the L5 nerve root. Patients with a weak or absent tibialis anterior muscle will have a drop foot or a steppage gait. The tibialis anterior muscle causes dorsiflexion and inversion of the foot and ankle.Correct Answer: L4
683. (1050) Q2-1357:
The patellar tendon reflex is primarily transmitted through which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
Although the patellar tendon reflex is primarily transmitted through the L4 nerve root, the L2 and L3 nerve roots also contribute to the fibers. There is a weak reflex if the L4 nerve root is completely cut, even if there are still L2 and L3 fibers. Patellar tendon reflex is seldom completely absent unless the patient has primary muscle or anterior horn lesions.Correct Answer: L4
4) L5
It is important to remember the sensory dermatomes when examining patients. The medial aspect of the leg, foot, and great toe are supplied by the L4 nerve root. The tibial crest separates the L4 and L5 dermatomes on the leg.
Remember:
L4 Medial aspect of the leg, foot, and great toe L5 Lateral aspect of the leg and toes 2 to 4
S1 Lateral aspect of the fifth toe Correct Answer: L4
685. (1052) Q2-1359:
The extensor hallucis longus muscle is innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The extensor hallucis longus muscle is primarily innervated by the L5 nerve root. The L5 nerve root innervates the following muscles:
Extensor hallucis longus muscle
Extensor digitorum longus and brevis muscles Gluteus medius muscle
Correct Answer: L5
686. (1053) Q2-1360:
The extensor digitorum longus and brevis muscles are primarily innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The extensor digitorum longus and brevis muscles are primarily innervated by the L5 nerve root. The L5 nerve root innervates the following muscles:
Extensor hallucis longus muscle
Extensor digitorum longus and brevis muscles Gluteus medius muscle
Correct Answer: L5
1) L1
3) L3
2) L2
5) L5
4) L4
The gluteus medius muscle principally receives its innervation from the L5 nerve root through the superior gluteal nerve. Although the principal innervation is from L5, L4 and S1 nerve roots also contribute to the innervation.Correct Answer: L5
688. (1055) Q2-1362:
Testing of the L5 nerve root is accomplished through the:
1) Patellar tendon reflex
3) Tibialis posterior reflex
2) Achilles tendon reflex
5) Beevor sign
4) Superficial anal reflex
There is not a well-defined reflex arc for the L5 nerve root. The tibialis posterior reflex may be elicited at times, and this reflex is mediated through the L5 nerve root.
Remember the other reflexes as well: Patellar tendon L4
Achilles tendon S1
Superficial anal reflex S2, S3, and S4
Beevor sign refers to asymmetry of the segmental innervation of the rectus abdominus muscles. This is noted when a patient performs a sit-up and unilateral segmental nerve root loss is noted.Correct Answer: Tibialis posterior reflex
689. (1056) Q2-1363:
The skin on the lateral aspect of the leg and the dorsum of the foot between the second and fourth toes is innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The L5 dermatome covers the skin on the lateral leg and dorsum of the foot from the lateral border of the great toe to the medial border of the little toe.
Remember:
L4 Medial aspect of the leg, foot, and great toe L5 Lateral aspect of the leg and toes 2 to 4
S1 Lateral aspect of the fifth toe Correct Answer: L5
4) S1
The peroneus brevis and longus muscles are principally innervated by the S1 nerve root through the superficial peroneal nerve. Although the innervation is principally through the S1 nerve root, the nerve is derived from the L5 and S2 nerve roots, as well.
Remember that the muscles principally innervated by the S1 nerve root include: Peroneus longus and brevis muscles
Gastrocnemius-soleus complex Gluteus maximus muscle
Correct Answer: S1
691. (1058) Q2-1365:
The medial and lateral gastrocnemius muscles principally receive their innervation through which of the following nerve roots:
1) L3
3) L5
2) L4
5) S2
4) S1
The medial and lateral gastrocnemius muscles are principally supplied by the S1 nerve root through the tibial nerve. There are also nerve fiber contributions from L5 and S2.
Remember that the muscles principally innervated by the S1 nerve root include: Peroneus longus and brevis muscles
Gastrocnemius-soleus complex Gluteus maximus muscle
Correct Answer: S1
692. (1059) Q2-1366:
The Achilles tendon reflex (ankle reflex) is transmitted through which of the following nerve roots:
1) L4
3) S1
2) L5
5) S3
4) S2
The Achilles tendon reflex is based upon the triceps muscle group (medial and lateral gastrocnemius muscles and soleus muscle) and is transmitted through the S1 nerve root.
Remember:
Patellar tendon reflex L4 Posterior tibial reflex L5 Achilles tendon reflex S1
Correct Answer: S1
1) L2, L3, and L4
3) L4, L5, and S1
2) L4 and L5
5) S2 and S3
4) L5, S1, and S2
The intrinsic muscles of the foot are innervated by the S2 and S3 nerve roots. These muscles are difficult to test. Clawing of the toes occurs with intrinsic muscle paralysis.
Remember the following nerve roots and the structures that they innervate:
L5, S1 and S2 Hip extension: Gluteus maximus muscle
L5, S1, and S2 Foot plantarflexion
L5, S1 and S2 Foot eversion
L4, L5, and S1 Hip abduction: Gluteus medius muscle
L4, L5 Foot dorsiflexion
L4, L5 Foot inversion
L2, L3, and L4 Hip adduction
L2, L3, and L4 Knee extension
L1, L2, and L3 Hip flexion: Iliopsoas muscle Correct Answer: S2 and S3
694. (1061) Q2-1368:
Perianal sensation is derived from which of the following nerve roots:
1) L2, L3, and L4
3) L5, S1, and S2
2) L3, L4, and L5
5) S2, S3, S4, and S5
4) S1, S2, and S3
Perianal sensation is derived from the S2, S3, S4, and S5 nerve roots. The sensory distribution is as follows:
S4-S5 Innermost perianal ring
S3 Middle perianal ring
S2 Outermost perianal ring Correct Answer: S2, S3, S4, and S5
1) T2
3) T7
2) T4
5) T12
4) T10
It is important to know the sensory segmental levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, a clinician should also know the sensory levels.
Remember:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin
Correct Answer: T4
696. (1063) Q2-1370:
Which of the following sensory segmental levels corresponds to sensation at the xiphoid process:
1) T2
3) T7
2) T4
5) T12
4) T10
The skin over the xiphoid process area is innervated by the T7 nerve root.
It is important to know the sensory segmental levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, a clinician should also know the sensory levels.
Remember:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin
Correct Answer: T7
1) T2
3) T7
2) T4
5) T12
4) T10
The skin of the umbilicus is innervated by the T10 sensory segmental level.
It is important to know the sensory segmental levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, a clinician should also know the sensory levels.
Remember:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin
Correct Answer: T10
698. (1065) Q2-1372:
The skin over the groin is innervated by which of the following sensory segmental levels:
1) T2
3) T7
2) T4
5) T12
4) T10
The skin over the groin is innervated by the T12 sensory segmental level.
It is important to know the sensory segmental levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, a clinician should also know the sensory levels.
Remember:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin
Correct Answer: T12
1) T10, T11, and T12
3) L2, L3, and L4
2) L1, L2, and L3
5) L5, S1, and S2
4) L4, L5, and S1
The iliopsoas muscle is the main flexor of the hip, and it receives principal innervation from the L1, L2, and L3 levels. Remember:
L5, S1 and S2 Hip extension: Gluteus maximus muscle
L5, S1, and S2 Foot plantarflexion
L5, S1 and S2 Foot eversion
L4, L5, and S1 Hip abduction: Gluteus medius muscle
L4 and L5 Foot dorsiflexion
L4 and L5 Foot inversion
L2, L3, and L4 Hip adduction
L2, L3, and L4 Knee extension
L1, L2, and L3 Hip flexion: Iliopsoas muscle Correct Answer: L1, L2, and L3
700. (1067) Q2-1374:
Which of the following segmental levels innervates the quadriceps muscle:
1) T10, T11, and T12
3) L2, L3, and L4
2) L1, L2, and L3
5) L5, S1, and S2
4) L4, L5, and S1
The quadriceps muscle is innervated by the femoral nerve from the L2, L3, and L4 segmental levels. Remember:
⢠L5, S1 and S2 Hip extension: Gluteus maximus muscle ⢠L5, S1, and S2 Foot plantarflexion
⢠L5, S1 and S2 Foot eversion
⢠L4, L5, and S1 Hip abduction: Gluteus medius muscle ⢠L4 and L5 Foot dorsiflexion
⢠L4 and L5 Foot inversion ⢠L2, L3, and L4 Hip adduction ⢠L2, L3, and L4 Knee extension
⢠L1, L2, and L3 Hip flexion: Iliopsoas muscle Correct Answer: L2, L3, and L4
1) T12
3) L2
2) L1
5) L4
4) L3
The skin over the thigh is innervated by the L1, L2, and L3 sensory segmental levels. Remember:
L1 Thigh, proximal third, and anterior
L2 Thigh, middle, and anterior
L3 Thigh, distal third, and anterior Correct Answer: L3
702. (1069) Q2-1376:
The skin of the anterior middle third of the thigh is innervated by which of the following sensory segmental levels:
1) T12
3) L2
2) L1
5) L4
4) L3
The skin over the thigh is innervated by the L1, L2, and L3 sensory segmental levels. Remember:
L1 Thigh, proximal third, and anterior
L2 Thigh, middle, and anterior
L3 Thigh, distal third, and anterior Correct Answer: L2
703. (1070) Q2-1377:
The skin of the proximal one-third of the anterior thigh just distal to the inguinal ligament is innervated by which of the following sensory segmental levels:
1) T12
3) L2
2) L1
5) L4
4) L3
The skin over the thigh is innervated by the L1, L2, and L3 sensory segmental levels. Remember:
⢠L1 Thigh, proximal third, and anterior ⢠L2 Thigh, middle, and anterior
⢠L3 Thigh, distal third, and anterior Correct Answer: L1
The tibialis anterior muscle is principally innervated by which of the following segmental levels:
1) L1
3) L3
2) L2
5) L5
4) L4
The tibialis anterior muscle is primarily innervated by the L4 nerve root. The tibialis anterior muscle also receives innervation from L5. Patients with a weak or absent tibialis anterior muscle will have a drop foot or a steppage gait. The tibialis anterior muscle causes dorsiflexion and inversion of the foot and ankle.Correct Answer: L4
(1244) Q2-1614:
The patellar tendon reflex is primarily transmitted through which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
Although the patellar tendon reflex is transmitted primarily through the L4 nerve root, the L2 and L3 nerve roots also contribute to the fibers. A weak reflex is present if the L4 nerve root is completely cut even if there are still fibers of L2 and L3. This reflex is seldom completely absent unless the patient has primary muscle or anterior horn lesions.Correct Answer: L4
(1245) Q2-1615:
The skin on the medial aspect of the leg and great toe is innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
It is important to remember the sensory dermatomes when examining patients. The medial aspect of the leg, foot, and great toe are supplied by the L4 nerve root. The tibial crest separates the L4 and L5 dermatomes on the leg.
Note:
L4 Medial aspect of leg, foot, and great toe
L5 Lateral aspect of the leg and toes two through four S1 Lateral aspect of the fifth toe
Correct Answer: L4
(1246) Q2-1616:
The extensor hallucis longus muscle is innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The extensor hallucis muscle is primarily innervated by the L5 segmental level. Remember that the L5 nerve root innervates the following muscles:
Extensor hallucis longus
Extensor digitorum longus and brevis Gluteus medius
Correct Answer: L5
(1247) Q2-1617:
The extensor digitorum longus and brevis muscles are primarily innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The extensor digitorum longus and brevis muscles are primarily innervated by the L5 nerve root. Remember that the L5 nerve root innervates the following muscles:
Extensor hallucis longus
Extensor digitorum longus and brevis Gluteus medius
Correct Answer: L5
(1248) Q2-1618:
The gluteus medius muscle is principally innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The gluteus medius muscle principally receives innervation from the L5 nerve root through the superior gluteal nerve. Although the principal innervation is from L5, there are contributions from L4 and S1.Correct Answer: L5
(1249) Q2-1619:
Testing for the L5 nerve root can be accomplished through which of the following:
1) Patellar tendon reflex
3) Superficial anal reflex
2) Achilles tendon reflex
5) Beevor's sign
4) Tibialis posterior reflex
There is not a well-defined reflex arc for the L5 nerve root. The tibialis posterior reflex can sometimes be elicited, and this reflex is mediated through the L5 nerve root.
Remember the other reflexes as well:
Patellar tendon L4
Achilles tendon S1
Superficial anal reflex S2, S3, S4
Beevorâs sign refers to asymmetry of the segmental innervation of the rectus abdominus muscles. When a patient performs a sit-up, there is unilateral segmental nerve root loss.Correct Answer: Tibialis posterior reflex
The skin on the lateral aspect of the leg and the dorsum of the foot between the second and fourth toes is innervated by which of the following nerve roots:
1) L1
3) L3
2) L2
5) L5
4) L4
The L5 dermatome covers the skin on the lateral leg and dorsum of the foot from the lateral border of the great toe to the medial border of the little toe.
Note:
L4 Medial aspect of leg, foot, and great toe
L5 Lateral aspect of the leg and toes two through four S1 Lateral aspect of the fifth toe
Correct Answer: L5
712. (1251) Q2-1621:
The peroneus longus and brevis muscles are innervated by which of the following nerve roots:
1) L3
3) L5
2) L4
5) S2
4) S1
The peroneus brevis and longus muscles are principally innervated by the S1 nerve root through the superficial peroneal nerve. Although the innervation is principally S1, the nerve is derived from the L5 and S2 nerve roots, as well.
Remember that the muscles principally innervated by the S1 nerve root are: Peroneus longus and brevis
Gastrocnemius-soleus complex Gluteus maximus
Correct Answer: S1
713. (1252) Q2-1622:
The medial and lateral gastrocnemius muscles principally receive their innervation through which of the following nerve roots:
1) L3
3) L5
2) L4
5) S2
4) S1
The medial and lateral gastrocnemius muscles are principally supplied by the S1 nerve root through the tibial nerve. Although the innervation is principally S1, the nerve is derived from the L5 and S2 nerve roots, as well.
Remember that the muscles principally innervated by the S1 nerve root are: Peroneus longus and brevis
Gastrocnemius-soleus complex Gluteus maximus
Correct Answer: S1
The Achilles tendon reflex (ankle reflex) is transmitted through which of the following nerve roots:
1) L4
3) S1
2) L5
5) S3
4) S2
The Achilles tendon reflex is based upon the triceps muscle group (medial and lateral gastrocnemius muscles and soleus muscle) and is transmitted through the S1 nerve root.
Note the reflexes and the associated nerve roots:
Patellar tendon reflex L4
Posterior tibial reflex L5
Achilles tendon reflex S1 Correct Answer: S1
715. (1254) Q2-1624:
Which of the following groups of nerve roots innervates the intrinsic muscles of the foot:
1) L2, L3, and L4
3) L4, L5, and S1
2) L4 and L5
5) S2 and S3
4) L5, S1, and S2
The intrinsic muscles of the foot are innervated by the S2 and S3 nerve roots. These muscles are difficult to test. Clawing of the toes occurs with intrinsic muscle paralysis.
The following nerve roots innervate important structures: L5, S1, and S2 Hip extension: gluteus maximus
L5, S1, and S2 Foot plantar flexion L5, S1, and S2 Foot eversion
L4, L5, and S1 Hip abduction: gluteus medius L4, L5 Foot dorsiflexion
L4, L5 Foot inversion L2, L3, and L4 Hip adduction L2, L3, and L4 Knee extension
L1, L2, and L3 Hip flexion: iliopsoas Correct Answer: S2 and S3
716. (1255) Q2-1625:
Perianal sensation is derived from which of the following nerve roots:
1) L2, L3, and L4
3) L5, S1, and S2
2) L3, L4, and L5
5) S2, S3, S4, and S5
4) S1, S2, and S3
Perianal sensation is derived from the S2, S3, S4, and S5 nerve roots. The sensory distribution is as follows:
S4-S5 Innermost perianal ring S3 Middle perianal ring
S2 Outermost perianal ring Correct Answer: S2, S3, S4, and S5
717. (1256) Q2-1626:
Which of the following sensory segmental levels corresponds with the nipple line:
1) T2
3) T7
2) T4
5) T12
4) T10
It is important to know the sensory levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, the clinician should also know the sensory levels.
Note:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin Correct Answer: T4
718. (1257) Q2-1627:
Which of the following segmental nerve levels corresponds to sensation at the xiphoid process:
1) T2
3) T7
2) T4
5) T12
4) T10
The skin over the xiphoid process area is innervated by the T7 nerve root.
It is important to know the sensory levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, the clinician should also know the sensory levels.
Note:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin Correct Answer: T7
1) T2
3) T7
2) T4
5) T12
4) T10
The skin of the umbilicus is innervated by the T10 level.
It is important to know the sensory levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, the clinician should also know the sensory levels.
Note:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin Correct Answer: T10
720. (1259) Q2-1629:
The skin over the groin is innervated by which of the following segmental levels:
1) T2
3) T7
2) T4
5) T12
4) T10
The skin over the groin is innervated by the T12 level.
It is important to know the sensory levels to localize pathologic processes. In addition to knowing the innervation of selected muscles and the deep tendon reflexes, the clinician should also know the sensory levels.
Note:
T4 Nipple line
T7 Xiphoid process
T10 Umbilicus
T12 Groin Correct Answer: T12
1) T10, T11, T12
3) L2, L3, L4
2) L1, L2, L3
5) L5, S1, S2
4) L4, L5, S1
The iliopsoas muscle is the main flexor of the hip. The iliopsoas muscle receives innervation from the L1, L2, and L3 levels. One should remember the following nerve roots that innervate important structures:
L5, S1, and S2 Hip extension: gluteus maximus L5, S1, and S2 Foot plantar flexion
L5, S1, and S2 Foot eversion
L4, L5, and S1 Hip abduction: gluteus medius L4, L5 Foot dorsiflexion
L4, L5 Foot inversion L2, L3, and L4 Hip adduction L2, L3, and L4 Knee extension
L1, L2, and L3 Hip flexion: iliopsoas Correct Answer: L1, L2, L3
722. (1261) Q2-1631:
Which of the following segmental levels innervates the quadriceps muscle:
1) T10, T11, T12
3) L2, L3, L4
2) L1, L2, L3
5) L5, S1, S2
4) L4, L5, S1
The quadriceps muscle is innervated by the femoral nerve from the L2, L3, and L4 levels. One should remember the following nerve roots that innervate important structures:
L5, S1, and S2 Hip extension: gluteus maximus L5, S1, and S2 Foot plantar flexion
L5, S1, and S2 Foot eversion
L4, L5, and S1 Hip abduction: gluteus medius L4, L5 Foot dorsiflexion
L4, L5 Foot inversion L2, L3, and L4 Hip adduction L2, L3, and L4 Knee extension
L1, L2, and L3 Hip flexion: iliopsoas Correct Answer: L2, L3, L4
1) T12
3) L2
2) L1
5) L4
4) L3
The skin over the thigh is innervated by L1, L2, and L3. Note:
L1 Thigh, proximal third, anterior L2 Thigh, middle, anterior
L3 Thigh, distal third, anterior Correct Answer: L3
724. (1263) Q2-1633:
The skin of the anterior middle third of the thigh is innervated by which of the following levels:
1) T12
3) L2
2) L1
5) L4
4) L3
The skin over the anterior middle third of the thigh is innervated by L1, L2, and L3. Note:
L1 Thigh, proximal third, anterior L2 Thigh, middle, anterior
L3 Thigh, distal third, anterior Correct Answer: L2
725. (1264) Q2-1634:
The skin of the proximal one-third of the anterior thigh just distal to the inguinal ligament is innervated by which of the following levels:
1) T12
3) L2
2) L1
5) L4
4) L3
The skin of the proximal one-third of the anterior thigh just distal to the inguinal ligament is innervated by L1, L2, and L3. Note:
L1 Thigh, proximal third, anterior L2 Thigh, middle, anterior
L3 Thigh, distal third, anterior Correct Answer: L1
1) Inhibiting of cell wall synthesis
3) Inhibiting RNA synthesis
2) Selectively targeting bacterial topoisomerases (inhibit DNA replication)
5) Poisoning cytochrome C system
4) Inhibiting ribosomal translation
The fluoroquinolone class of antibiotics selectively target bacterial topoisomerases. Topoisomerases maintain the correct amount of supercoiling of DNA in both replicating and nonreplicating areas of the chromosomes.
Fluoroquinolones Second generation
Ciprofloxacin, ofloxacin, and lomefloxacin
Third generation
Sparfloxacin and levofloxacin
Fourth generation
Trovofloxacin, gatifloxacin, and moxifloxacin
Correct Answer: Selectively targeting bacterial topoisomerases (inhibit DNA replication)
727. (1266) Q2-1636:
The fluoroquinolone class of antibiotics, including ofloxacin and ciprofloxacin, is especially useful (considered drug of choice) for osteomyelitis caused by which of the following organisms:
1) Pseudomonas
3) Staphylococcus epidermidis
2) Staphylococcus aureus
5) Streptococcus
4) Enterobacteriaceae
Ofloxacin and ciprofloxacin have been studied in the treatment of post-traumatic osteomyelitis. When compared with parenteral antibiotics, the cure rate was 80% for the fluoroquinolones and 85% for the parenteral antibiotics. The cure rate for the fluoroquinolones was even higher against Enterobacteriaceae. They are considered the drug of choice for osteomyelitis according to the referenced article.Correct Answer: Enterobacteriaceae
adverse effects:
1) Young women
3) Diabetic patients
2) Children
5) Patients with sickle cell anemia
4) Elderly patients
Fluoroquinolones may cause side effects to the musculoskeletal system that include arthralgias, chondrotoxicity, and tendinopathy. Cartilage damage was found in animal studies at therapeutic doses. The cartilage cells of the physeal plate were damaged.
Cartilage blistering, erosions, matrix degeneration, and chondrocyte loss were also present. The fluoroquinolones are not to be used in children, pregnant women, and nursing mothers unless under special circumstances (such as drug resistance in children with cystic fibrosis).
The fluoroquinolones are safe in the other groups of patients. One should remember the following: Light-headedness and dizziness may occur in young women.
Nausea, vomiting, and diarrhea are the most common complications.
Nonsteroidal anti-inflammatory drugs taken in combination will worsen side effects. Photosensitivity may occur.
Achilles tendonitis and rupture may occur.
Correct Answer: Children
729. (1268) Q2-1638:
Which of the following musculoskeletal complications may occur in patients taking fluoroquinolones, such as ciprofloxacin:
1) Osteomalacia
3) Joint laxity
2) Osteoporosis
5) Parethesias
4) Tendon ruptures
Fluoroquinolones may cause side effects to the musculoskeletal system that include arthralgias, chondrotoxicity, and tendinopathy.
Achilles tendonitis and rupture is the most common tendinopathy associated with fluoroquinolone use (usually ciprofloxacin). Fifty percent of cases are bilateral. The interval to rupture is between 2 and 60 days.
Patients at increased risk include:
Patients older than 60 years of age Patients with diabetes
Patients with impaired renal function
Patients who partake in strenuous sports activities Correct Answer: Tendon ruptures
1) Receptor activator of nuclear factor-kappa B (RANK)
3) Bone morphogenetic protein 7
2) Osteoprotegerin
5) Parathyroid hormone related protein (PTHrP)
4) Core binding factor alpha 1 (Cbfa1)
Four proteins that regulate osteoclast activation have been discovered:
Receptor activator of nuclear factor-kappa B (RANK) binds to a receptor on osteoclast precursor cells and positively effects their final differentiation into osteoclasts.
Osteoprotegerin is a soluble decoy receptor that resembles RANK and inhibits osteoclasts.
Tumor necrosis factor-related activation induced cytokine (TRANCE)
Osteoclast differentiation factor
Note:
Core binding factor alpha 1 (Cbfa1) is a transcription factor (coded by the Cbfa1 gene) that is necessary and sufficient for differentiation of cells into osteoblasts and facilitates chondrocyte differentiation during enchondral bone formation.Correct Answer: Receptor activator of nuclear factor-kappa B (RANK)
731. (1270) Q2-1640:
Which of the following proteins negatively effects precursor cells to form osteoclasts:
1) Receptor activator of nuclear factor-kappa B (RANK)
3) Bone morphogenetic protein 7
2) Osteoprotegerin
5) Parathyroid hormone related protein (PTHrP)
4) Core binding factor alpha 1 (Cbfa1)
Four proteins that regulate osteoclast activation have been discovered:
Receptor activator of nuclear factor-kappa B (RANK) binds to a receptor on osteoclast precursor cells and positively effects their final differentiation into osteoclast activation.
Osteoprotegerin is a soluble decoy receptor that resembles RANK and inhibits osteoclasts.
Tumor necrosis factor-related activation induced cytokine (TRANCE)
Osteoclast differentiation factor
Note:
Core binding factor alpha 1 (Cbfa1) is a transcription factor (coded by the Cbfa1 gene) that is necessary and sufficient for differentiation of cells into osteoblasts and facilitates chondrocyte differentiation during enchondral bone formation.Correct Answer: Osteoprotegerin
732. (1271) Q2-1641:
Which of the following proteins or genes is necessary for bone formation and induces osteocalcin (expressed exclusively by osteoblasts):
1) Sox-9 gene
3) Receptor activator of nuclear factor-kappa B (RANK)
2) Core binding factor alpha 1 (Cbfa1)
5) Osteoprotegerin
Tumor necrosis factor-related activation induced cytokine (TRANCE)
Core binding factor alpha 1 (Cbfa1) and its gene (Cbfa1) have been described as anabolic regulators of bone. Cbfa1 is a transcription factor and is responsible for the differentiation of precursor cells into osteoblasts. It also enhances differentiation of chondrocytes during enchondral bone formation. When there is deficiency of Cbfa1 there can be abnormal bone development, as in clediocranial dysplasia.Correct Answer: Core binding factor alpha 1 (Cbfa1)
1) 1,000
3) 10,000
2) 5,000
100,000
4) 30,000
The human genome is composed of approximately 30,000 unique genes. Each gene is composed of a promotor or regulator region and a transcriptional or coding region. Regulatory proteins or transcription factors bind to the promoter region of the gene to signal the beginning of transcription of the DNA into RNA or repress the expression of the gene. The coding region contains both introns and exons. Exon sequences of the gene directly code for the proteins, and the introns are spacers. The intron sequences are enzymatically removed from the newly transcribed messenger RNA by a splicing mechanism.Correct Answer: 30,000
734. (1273) Q2-1643:
Which of the following portions of a gene directly codes for the messenger RNA for eventual translation into proteins on the ribosome:
1) Promoter region
3) Exon
2) Intron
5) Activator or repressor binding site
4) Coding region
The human genome is composed of approximately 30,000 unique genes. Each gene is composed of a promotor or regulator region and a transcriptional or coding region. Regulatory proteins or transcription factors bind to the promoter region of the gene to signal the beginning of transcription of the DNA into RNA or repress the expression of the gene. The coding region contains both introns and exons. Exon sequences of the gene directly code for the proteins, and the introns are spacers. The intron sequences are enzymatically removed from the newly transcribed messenger RNA by a splicing mechanism.Correct Answer: Exon
735. (1910) Q2-2320:
Which of the following occurs in Pagetâs disease:
1) Inadequate mineralization of newly formed bone
3) Normal osteoclastic activity with decreased osteoblastic activity
2) Low bone mass and microarchitectural deterioration of bone
5) Increased osteoclastic activity and increased bone formation
4) Increased osteoclastic activity and normal osteoblastic activity
Pagetâs disease is a remodeling disease in which there is marked bone resorption by the osteoclast. The osteoblasts repair the bone in a mosaic pattern with thickened trabeculae and cement or remodeling lines. There is both increased osteoclastic activity and increased bone formation by the osteoblast.
Inadequate mineralization of newly formed bone is called osteomalacia. In children, there is decreased mineralization at the growth plate.
Osteoporosis refers to low bone mass and microarchitectural deterioration of bone. There are two types of osteoporosis:
High turnover osteoporosis is increased osteoclastic activity and normal osteoblastic activity. In high turnover, the osteoclasts resorb large amounts of bone and the osteoblasts are unable to replace the bone. One finds markers for high levels of bone resorption and bone formation in the serum and the urine.
Low turnover osteoporosis is normal osteoclastic activity with decreased osteoblastic activity. In low turnover, the osteoclastic activity is at the normal rate; however, there is insufficient osteoblastic activity to fill in the osteoclastic resorption cavities. The markers for osteoclastic resorption are normal and the markers for bone formation are decreased.
Correct Answer: Increased osteoclastic activity and increased bone formation
1) Serum alkaline phosphatase
3) Gamma-glutamyl transpeptidase
2) Aspartate aminotransferase and alanine aminotransferase
5) Urine N-telopeptide, pyridinoline, and deoxypyridinoline
4) Osteocalcin
Bone resorption is assessed by measuring the products of bone remodeling. N-telopeptide, pyridinoline, and deoxypyridinoline are collagen cross-link products that are released during bone turnover. These collagen cross-links can be measured in the urine. A new marker can be measured in the serum and is called carboxy terminal collagen cross-links (CrossLaps).
Bone formation is assessed with serum alkaline phosphastase and osteocalcin.
Liver function tests include aspartate aminotransferase, alanine aminotransferase, and gamma-glutamyl transpeptidase.Correct Answer: Urine N-telopeptide, pyridinoline, and deoxypyridinoline
737. (1912) Q2-2322:
Pagetâs disease is common in all of the following bones except:
1) Humerus
3) Femur
2) Spine
5) Pelvis
4) Hands and feet
Key features of Pagetâs disease:
Remodeling disease caused by excessive osteoclastic activity
Rarely diagnosed in patients younger than 40 years of age; most patients diagnosed after age 50 Most common sites include pelvis, femur, spine, skull, and tibia
Less common sites include clavicles, scapulae, ribs, and facial bones Rarely found in the hands and feet
Pagetic bone
is more susceptible to fracture is less compact
is more vascular
tends to bow in weight bearing areas
Geographic clustering (up to 4% in patients older than 55 years of age) England
Northern Europe North America
Australia, New Zealand
Rare in Asia, China, Indonesia, Malaysia, and sub-Saharan Africa Possibly a slow viral disease
RNA paramyxovirus (e.g., respiratory syncytial virus and measles) Correct Answer: Hands and feet
1) England
3) Northern Europe
2) United States
5) Sub-Saharan Africa
4) Australia
Key features of Pagetâs disease
Remodeling disease caused by excessive osteoclastic activity
Rarely diagnosed in patients younger than 40 years of age; most patients diagnosed after age 50 Most common sites include pelvis, femur, spine, skull, and tibia
Less common sites include clavicles, scapulae, ribs, and facial bones Rarely found in the hands and feet
Pagetic bone
is more susceptible to fracture is less compact
is more vascular
tends to bow in weight bearing areas
Geographic clustering (up to 4% in patients older than 55 years of age) England
Northern Europe North America
Australia, New Zealand
Rare in Asia, China, Indonesia, Malaysia, and sub-Saharan Africa Possibly a slow viral disease
RNA paramyxovirus (e.g., respiratory syncytial virus and measles) Correct Answer: Sub-Saharan Africa
739. (1914) Q2-2324:
Which of the following occurs in active Pagetâs disease:
1) Intense osteoclastic activity, intense osteoblastic activity
3) Intense osteoclastic activity, decreased osteoblastic activity
2) Decreased osteoclastic activity, decreased osteoblastic activity
5) Intense osteoclastic activity, normal osteoblastic activity
4) Decreased osteoclastic activity, increased osteoblastic activity
Marked bone resorption by the osteoclast and marked bone formation by the osteoblast occurs in active Pagetâs disease. The activities of the osteoclast and osteoblast are linked together.Correct Answer: Intense osteoclastic activity, intense osteoblastic activity
740. (1915) Q2-2325:
Osteocytic osteolysis refers to which of the following processes:
1) Loss of bone through decreased bone formation
3) Removal of bone by osteoclasts
2) Mobilization of poorly crystallized calcium salts without effect on bone matrix
5) Osteocyte-mediated resorption of bone matrix
4) Loss of bone by osteoclasts in multiple myeloma
Osteocytes do not directly resorb bone. Osteocytes have receptors for parathyroid hormone, and they mobilize poorly crystallized calcium salts that surround them without resorbing the bone matrix. The osteocytes connect with each other through long, thin cytoplasmic processes.Correct Answer: Mobilization of poorly crystallized calcium salts without effect on bone matrix
areas of maximum stress and strain:
1) Mast cells in bone marrow
3) Plasma cells
2) Osteoblasts
5) Osteocytes
4) Osteoclasts
Osteocytes respond to mechanical signals and transmit messages to other cells to increase bone remodeling.Correct Answer: Osteocytes
742. (1917) Q2-2327:
Receptor activator of nuclear factor âkB (RANK) is located on which of the following cells:
1) Osteoblasts
3) Osteocytes
2) Plasma cells
5) Osteoclast precursors
4) Active osteoclasts
The activation of osteoclasts is a complex process. Surface receptors on the osteoclast precursor cells are called RANK. Receptor activator of nuclear factor âkB ligand (RANKL) is expressed on the surface of osteoblasts/stromal cells. The RANKL proteins leave the osteoblast and attach to the RANK receptor on the osteoclast precursor. Macrophage colony stimulating factor then facilitates the production of active osteoclasts from the osteoclast precursor.
Osteoprotegerin (OPG) is an inhibitor that is produced on the cell surface of hematopoietic precursor cells and mature osteoclasts. OPG binds to RANK receptor to inhibit the activation of osteoclasts
RANKL
OPG
Stimulates osteoclast differentiation and osteoclast activity Inhibits osteoclast apoptosis
Induces hypercalcemia when injected Loss of expression induces:
Osteopetrosis
Tooth eruption defects
T and B cell differentiation defects
Soluble decoy receptor for RANKL Blocks osteoclast formation Reduces hypercalcemia
Overexpression induces osteopetrosis Loss of expression induces osteoporosis Prevents calcification of large arteries
Correct Answer: Osteoclast precursors
1) Inhibits osteoclast apoptosis
3) Activates osteoclast precursors
2) Inhibits osteoclast formation
5) Binds to receptor activator of nuclear factor âkB ligand (RANKL)
4) Induces hypercalcemia
The activation of osteoclasts is a complex process. Surface receptors on the osteoclast precursor cells are called RANK. Receptor activator of nuclear factor âkB ligand (RANKL) is expressed on the surface of osteoblasts/stromal cells. The RANKL proteins leave the osteoblast and attach to the RANK receptor on the osteoclast precursor. Macrophage colony stimulating factor then facilitates the production of active osteoclasts from the osteoclast precursor.
Osteoprotegerin (OPG) is an inhibitor that is produced on the cell surface of hematopoietic precursor cells and mature osteoclasts. OPG binds to RANK receptor to inhibit the activation of osteoclasts.
OPG
Soluble decoy receptor for RANKL Blocks osteoclast formation Reduces hypercalcemia
Overexpression induces osteopetrosis Loss of expression induces osteoporosis Prevents calcification of large arteries
Correct Answer: Inhibits osteoclast formation
744. (1919) Q2-2329:
Which of the following proteins or hormones assists in the transport of calcium in the kidney against chemical and electrical gradients:
1) Calcitonin
3) Osteoprotegerin
2) Calbindin
5) Vitamin D3
4) Parathyroid hormone
Calbindin, a vitamin D dependent and calcium binding protein, assists in the transport of calcium against chemical and electrical gradients. Most regulation calcium resorption in the kidney occurs in the distal convoluted segment.Correct Answer: Calbindin
745. (1920) Q2-2330:
Which of the following is the rate-limiting step in the production of biologically active Vitamin D:
1) 25 hydroxylation in the liver
3) Conversion of 7 dehydrocholesterol to vitamin D3 in the skin
2) Absorption of calcium in the duodenum
5) Absorption of calcium in the jejunum
4) 1 hydroxylation in the kidney
The addition of a second hydroxyl group at the 1 position to 25 hydroxy vitamin D3 is the rate-limiting step in the formation of the active from of vitamin D3. Impaired renal function is common in older individuals.Correct Answer: 1 hydroxylation in the kidney
produced by osteoblasts:
1) Parathyroid hormone
3) Thyroid hormone
2) 25 hydroxyvitamin D3
5) Calcitonin
4) 1,25 dihydroxyvitamin D3
The active from of vitamin D (1,25 dihydroxyvitamin D3) regulates the control of RANKL production by the osteoblast.
The activation of osteoclasts is a complex process. Surface receptors on the osteoclast precursor cells are called RANK. Receptor activator of nuclear factor âkB ligand (RANKL) is expressed on the surface of osteoblasts/stromal cells. The RANKL proteins leave the osteoblast and attach to the RANK receptor on the osteoclast precursor. Macrophage colony stimulating factor then facilitates the production of active osteoclasts from the osteoclast precursor.Correct Answer: 1,25 dihydroxyvitamin D3
747. (1922) Q2-2332:
Which of the following proteins or vitamins influences growth plate chondrocyte maturation as a potent mitogen in the proliferative zone:
1) 1,25 dihydroxyvitamin D3
3) Insulin
2) 24,25 dihydroxyvitamin D3
5) Calcitonin
4) 1 hydroxyvitamin D3
Traditionally, 24,25 dihydroxyvitamin D3 was considered an inactive form of vitamin D. Recent studies suggest that 24,25 dihydroxyvitamin D3 influences growth plate chondrocyte maturation as a potent mitogen in the proliferative zone and may also contribute to bone formation and fracture repair.Correct Answer: 24,25 dihydroxyvitamin D3
748. (1923) Q2-2333:
Which of the following cells has receptors for parathyroid hormone:
1) Osteocytes
3) Plasma cells
2) Osteoclasts
5) Osteoclast precursor cells
4) Osteoblasts
Osteoblasts have receptors for parathyroid hormone. Once stimulated, the cells release interleukin-6 (IL-6). IL-6 signals osteoclasts to resorb bone. The osteoblasts secrete neutral proteases that degrade the osteoid surface. Osteoclasts then attach to the bone surface and secrete acid proteases that degrade the bone matrix. Parathyroid hormone related protein increases osteoblast expression of receptor activator of nuclear factor âkB ligand (RANKL). RANKL binds to osteoclast precursor cells for the formation of active osteoclasts.Correct Answer: Osteoblasts
749. (1924) Q2-2334:
Parathyroid hormone stimulates which of the following cells to secrete neutral protease that degrades the osteoid bone surface:
1) Osteoblasts
3) Osteoclasts
2) Mast cells
5) Osteoclast precursor cells
4) Osteocytes
Osteoblasts have receptors for parathyroid hormone. Osteoblasts have neutral proteases that begin the degradation of the osteoid matrix. Once stimulated, the cells release interleukin-6 (IL-6). IL-6 signals osteoclasts to resorb bone. The osteoblasts secrete neutral proteases that degrade the osteoid surface. Osteoclasts then attach to the bone surface and secrete acid proteases that degrade the bone matrix. Parathyroid hormone related protein increases osteoblast expression of receptor activator of nuclear factor âkB ligand (RANKL). RANKL binds to osteoclast precursor cells for the formation of active osteoclasts.Correct Answer: Osteoblasts
1) Osteoprotegerin
3) Interleukin-6
2) 1,25 dihydroxyvitamin D3 production
5) Receptor activator of nuclear factor âkB ligand (RANKL)
4) Kidney 1 alpha-hydroxylase
Parathyroid hormone inhibits the production of osteoprotegerin. Osteoprotegerin is a decoy inhibitor of the receptor activator of nuclear factor âkB. Osteoprotegerin inhibits osteoclast activation.Correct Answer: Osteoprotegerin
751. (1926) Q2-2336:
Osteoclasts have receptors for which of the following:
1) 1,25 dihydroxyvitamin D3
3) Osteoprotegerin
2) Parathyroid hormone
5) Calcitonin
4) Receptor activator of nuclear factor âkB
Osteoclasts have receptors for calcitonin. Calcitonin causes osteoclasts to shrink in size and reduces their ability to resorb bone.Correct Answer: Calcitonin
752. (1927) Q2-2337:
After oophorectomy or menopause, bone loss per year is estimated to be:
1) 0.3% to 0.5%
3) 5% to 10%
2) 2% to 3%
5) 15% to 20%
4) 10% to 15%
The normal estimated age-related bone loss per year is 0.5%. After oophorectomy or during the first 6 to 8 years after menopause, bone loss can be as high as 2.0% to 3.0% per year.Correct Answer: 2% to 3%
753. (1928) Q2-2338:
Estrogen deficiency results in which of the following:
1) Increased interleukin-6 (IL-6) expression
3) Decreased IL-6 expression
2) Increased osteoprotegerin (OPG) expression
5) Decreased macrophage colony-stimulating factor (M-CSF) expression
4) Decreased receptor activator of nuclear factor âkB ligand (RANKL)
Estrogen deficiency results in increased bone resorption. An increase in IL-6 expression stimulates osteoclasts to resorb bone.
An increase in M-CSF and RANKL results in increased osteoclastic activity. OPG decreases osteoclastic activity as a decoy inhibitor of RANK.Correct Answer: Increased interleukin-6 (IL-6) expression
1) Osteoclasts
3) Osteoblasts
2) Osteoclast precursor cells
5) Mast cells
4) Osteocytes
Osteoblasts have receptors for androgens. Although androgens prevent bone resorption and may increase bone mass, the process is not understood at this time.Correct Answer: Osteoblasts
755. (1930) Q2-2340:
Corticosteroids decrease bone mass through which of the following mechanisms:
1) Inhibiting calcium absorption in the intestines
3) Increasing calcium binding proteins
2) Decreasing calcium excretion in the kidneys
5) Increasing bone resorption at high doses
4) Increasing overall protein synthesis
Corticosteroids decrease overall protein synthesis. In the intestines, corticosteroids decrease calcium-binding proteins, hence decreasing the absorption of calcium.
Corticosteroids:
Decrease overall protein synthesis Increase calcium excretion in the kidney
Inhibit bone formation and absorption at high doses
With the above changes, a state of secondary hyperparathyroidism exists. Correct Answer: Inhibiting calcium absorption in the intestines
756. (1931) Q2-2341:
Which of the following defines osteoporosis according to the World Health Organization:
1) 0.5 to 1.0 standard deviation (SD) below age-matched controls
3) 1.0 to 2.5 SD below age-matched controls
2) 1.0 to 2.0 SD below age-matched controls
5) 2.5 to 5.0 SD below age-matched controls
4) More than 2.5 SD below age-matched controls
Osteoporosis is a condition in which there is a deficiency of bone mass and microarchitectural deterioration of bone tissue. Osteoporosis is defined as a bone mass that is more than 2.5 SD below the mean for age-matched controls. Patients are considered osteopenic with mild to moderate bone deficiency with a bone density of 1.0 to 2.5 SD.Correct Answer: More than 2.5 SD below age-matched controls
1) Primarily occurs in patients older than 75 years of age
3) Cortical and trabecular bone are affected
2) Female to male ratio is 2:1
5) Related to estrogen deficiency rather than calcium intake
4) Low turnover osteoporosis
Type 1 osteoporosis is the most common form of osteoporosis and is found in women during postmenopausal years. Type 1 osteoporosis is related to estrogen deficiency rather than a problem in calcium intake or absorption.
Features of type 1 osteoporosis include: Female to male ratio is 6:1
High turnover osteoporosis
Bone loss rate of 2% to 3% per year for 6 to 10 years following menopause Trabecular bone is most affected
Related to estrogen deficiency rather than calcium intake
Correct Answer: Related to estrogen deficiency rather than calcium intake
758. (1933) Q2-2343:
Which of the following features is associated with type 2 osteoporosis:
1) High turnover osteoporosis
3) Loss of cortical and trabecular bone
2) Female to male ratio is 6:1
5) Greatest bone loss in the first 6 to 10 years following menopause
4) Related to estrogen deficiency
Type 1 osteoporosis is the most common form of osteoporosis and is found in women during postmenopausal years. Type 1 osteoporosis is related to estrogen deficiency rather than a problem in calcium intake or absorption.
Features of type 1 osteoporosis include: Female to male ratio is 6:1
High turnover osteoporosis
Bone loss rate of 2% to 3% per year for 6 to 10 years following menopause Trabecular bone is most affected
Related to estrogen deficiency rather than calcium intake
Type 2 osteoporosis, also called senile or involutional osteoporosis, is a low turnover osteoporosis and principally occurs in patients older than 75 years of age.
Features of type 2 osteoporosis include:
Female to male ratio is 2:1 Patients older than 75 years of age Low turnover osteoporosis
Trabecular and cortical bone affected Associated with hip fractures
Related to a lifelong deficiency of calcium Correct Answer: Loss of cortical and trabecular bone
1) Osteoblasts have estrogen receptors.
3) Estrogen decreases osteoclast activity.
2) Estrogen modulates calcium absorption and renal excretion.
5) The protective effect of estrogren therapy continues to prevent bone loss after therapy is discontinued.
4) Estrogen prevents osteoporosis in 80% of postmenopausal women.
Estrogen therapy is one of the main therapeutic interventions used to prevent osteoporosis in postmenopausal women. Features of estrogen interactions include:
Osteoblasts have estrogen receptors.
Estrogen indirectly affects calcium metabolism by modulating calcium absorption and renal excretion. Estrogen decreases osteoclast activity.
Estrogen prevents osteoporosis in 80% of postmenopausal women.
The protective effect of estrogren therapy ends when therapy is discontinued.
Correct Answer: The protective effect of estrogren therapy continues to prevent bone loss after therapy is discontinued.
760. (1935) Q2-2345:
Which of the following drugs is a selective estrogen receptor modulator:
1) Fosamax (alendronate sodium tablets, Merck & Co., Inc.)
3) Aredia (pamidronate disodium for injection, Novartis Pharmaceuticals Corporation)
2) Progestin
5) Alendronate sodium
4) Evista (raloxifene, Eli Lilly and Company)
A new class of selective estrogen receptor modulator acts as an antagonist in breast tissue and an agonist in bone. Raloxifene selectively stimulates estrogen receptors in bone and is an antagonist in breast tissue.
Progestin used in conjunction with estrogen opposes the action of estrogen and lowers the risk of endometrial cancer that might occur with estrogen therapy alone.
Aredia, Fosamax, and alendronate are biphosphonates that inhibit osteoclasts, thereby decreasing bone resorption.Correct Answer: Evista (raloxifene, Eli Lilly and Company)
761. (1936) Q2-2346:
Which of the following mechanisms of bisphosphonate action occurs when a bisphosphonate is used to treat osteoporosis:
1) Increasing calcium absorption in the intestines
3) Stimulating osteoblast precursors
2) Decreasing urinary excretion of calcium
5) Increasing phosphate reabsorption in the kidney
4) Binding to hydroxyapatite crystals
Bisphosphonates are effective in the treatment of osteoporosis because they bind to the hydroxyapatite crystals and inhibit crystal resorption.
Other effects of bisphosphonates include:
Reducing production of proteins and lysosomal enzymes by osteoclasts Reducing the formation of new bone remodeling units
Inducing osteoclast cell death
Reducing the formation of new osteoclasts
After 1 year of treatment, alendronate decreases fracture rates (hip, spine, and wrist) by 50%. Bone mass gains are modest â 2% to 4% per year in the vertebra and 1% to 2% per year in the hip.Correct Answer: Binding to hydroxyapatite crystals
1) Pruritus
3) Peripheral edema
2) Dizziness
5) Light sensitivity
4) Esophagitis and dyspepsia
The most significant side effect of biphosphonates is esophagitis and dyspepsia. Biphosphonates must be taken on an empty stomach with no oral intake for 30 minutes. In addition, patients should remain upright.Correct Answer: Esophagitis and dyspepsia
763. (1938) Q2-2348:
Which of the following conditions is characterized by decreased osteoclastic resorption of bone and cartilage with normal bone formation:
1) Type 1 osteoporosis
3) Osteopetrosis
2) Type 2 osteoporosis
5) Secondary hyperparathyroidism
4) Pagetâs disease
Osteopetrosis is a rare disorder in which there is decreased osteoclastic resorption of bone and cartilage with normal bone formation. There are a number of different forms of the condition.
The most common form of osteopetrosis is an autosomal dominant type with mild features (adult or tarda). Patients may have mild anemia, have one or more fractures, or be asymptomatic.
The juvenile form of osteopetrosis is a severe autosomal disorder. Children have multiple fractures, severe anemia, thrombocytopenia, and hepatosplenomegaly. Effected children are also immunocompromised.Correct Answer: Osteopetrosis
764. (1939) Q2-2349:
Which of the following is an effective medication for osteopetrosis:
1) Calcitonin
3) Fosamax (alendronate sodium tablets, Merck & Co., Inc.)
2) Alendronate
5) Interferon gamma-1
4) Calcium carbonate
Interferon gamma-1 is the only treatment for osteopetrosis that is approved by the Food and Drug Administration.Correct Answer: Interferon gamma-1
1) Cancellous bone, methylmethacrylate, cortical bone, titanium, and cobalt chrome
3) Methylmethacrylate, cancellous bone, titanium, cortical bone, and cobalt chrome
2) Cancellous bone, cortical bone, titanium, methylmethacrylate, and cobalt chrome
5) Titanium, cobalt chrome, methylmethacrylate, cancellous bone, and cortical bone
4) Titanium, cancellous bone, methylmethacrylate, cortical bone, and cobalt chrome
The proper sequence when listing common orthopedic biomaterials in order of increasing modulus is: Elastic Modulus
Cancellous bone Polyethylene Methylmethacrylate Cortical bone Titanium alloy Stainless steel Cobalt chrome
Correct Answer: Cancellous bone, methylmethacrylate, cortical bone, titanium, and cobalt chrome
766. (2329) Q2-2784:
Which of the following areas results in latitudinal physeal enlargement:
1) Proliferative zone
3) Reserve zone
2) Provisional calcification zone
5) Perichondrial ring of La Croix
4) Hypertrophic zone
The perichondrial ring of La Croix is the source of cells which differentiate into chondrocytes and results in latitudinal physeal enlargement.
The other answers refer to specific growth plate zones which have functions. The reserve zone is for matrix production and storage. The proliferative zone is for matrix production and cellular proliferation. The hypertrophic zone contains the zone of maturation, degeneration, and provisional calcification.
Correct Answer: Perichondrial ring of La Croix
767. (2330) Q2-2785:
The abrupt appearance of which of the following collagens heralds the onset of ossification in the physis:
1) Type I
3) Type X
2) Type VI
5) Type IX
4) Type II
The terminal hypertrophic chondrocytes in the hypertrophic zone produce Type X collagen. The appearance of Type X collagen heralds ossification. Remember that Type II collagen is the most abundant collagen in the hypertrophic zone.Correct Answer: Type X
Which of the following zones of the physis is involved in Salter Harris Type I and II fractures:
1) Proliferative zone
3) Reserve zone
2) Perichondrial ring
5) Zone of provisional calcification
4) Node of Ranvier
Salter Harris Type I and II fractures occur through the zone of provisional calcification or through the hypertrophic zone. The reserve and proliferative zone remain intact and growth can proceed normal after healing of the fracture.Correct Answer: Zone of provisional calcification
769. (2332) Q2-2787:
Which of the following is the most likely origin for the greater medullary artery:
1) Lower cervical segmental
3) Upper lumbar segmental
2) Middle thoracic segmental
5) Lower thoracic segmental
4) Upper thoracic segmental
The major part of the blood supply of the spinal cord is provided by the medullary or radicular arteries. The only feeder for the lower thoracic spinal cord is the greater medullary artery or artery of Adamkiwicz (T9-T11). One should remember that in the spine, the right-sided approach is preferred to avoid the aorta and segmental artery of Adamkiwicz.Correct Answer: Lower thoracic segmental
770. (2333) Q2-2788:
Enchondral ossification is responsible for mineralization in all of the following conditions except:
1) Heterotopic bone formation
3) Callus formation during fracture healing
2) Embryonic long bone development
5) Perichondrial bone formation
4) Cartilage degeneration in osteoarthritis
Enchondral bone formation or ossification is bone formation on a cartilage model. Enchondral bone formation occurs in embryonic long bone development, epiphyseal secondary center of ossification formation, callus formation during fracture healing, degenerating cartilage of osteoarthritis, calcifying cartilage tumors, and bone formed with use of demineralized bone matrix.
Intramembranous bone formation occurs in flat bone development (pelvis, clavicle, skull bones), bone formation during distraction osteogenesis, and perichondrial bone formation.Correct Answer: Perichondrial bone formation
771. (2334) Q2-2790:
Which of the following is true concerning cancellous bone:
1) It remodels through surface cells
3) It has high density
2) It has low surface area
5) It has a low metabolic rate and turnover
4) It is organized in osteons and lamellae
Cortical bone has a much greater density than cancellous bone. Therefore, it is stiffer and stronger. Cortical bone has a higher density than cancellous bone, is organized into osteons and lamellae, has low surface area, lower metabolic rate than cancellous bone, remodels through osteons, and accounts for much of the structural strength of bones.
Cancellous bone has a lower density than cortical bone, has an organization of lamellar bone, has a high surface area, higher metabolic rate than cortical bone, remodels through surface cells, and transmits forces in subchondral location.
Correct Answer: It remodels through surface cells
Which of the following statements is true regarding metaphyseal cortical bone formation in a child with open physes:
1) Cortical bone is formed by intramembranous bone formation.
3) Cortical bone is formed by coalescence of enchondral trabecular bone.
2) Cortical bone is formed by intramembranous and enchondral bone formation.
5) Cortical bone is formed from the groove of Ranvier.
4) Cortical bone is solely formed from the periosteal bone.
Cadet and colleagues studied the formation of cortical bone in the metaphyses of rabbits. They found that the metaphyseal cortical bone is formed by coalescence of enchondral trabecular bone.
Important points from this study include:
Metaphyseal cortical bone is formed by coalescence of enchondral trabecular bone. The coalescence is formed by an increased osteoblast surface.
The increased osteoblast surface is likely caused by factors from the periosteum.
The bone that is produced by the cells in the groove of Ranvier probably does not contribute to the metaphyseal cortical bone.
Correct Answer: Cortical bone is formed by coalescence of enchondral trabecular bone.
773. (2450) Q2-2915:
Which of the following molecules influences embryonic bone formation and fracture healing:
1) Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1)
3) Platelet derived growth factor (PDGF)
2) Transforming growth factor-beta (TGF-B)
5) Vascular endothelial growth factor (VEGF)
4) Interleukin-1 (IL-1)
Important concepts to remember regarding signaling proteins include:
Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1) influence embryonic bone formation and fracture healing. Vascular endothelial growth factor (VEGF) plays a role in cartilage hypertrophy at the growth plate and during fracture healing.
Transforming growth factor-beta (TGF-B) and platelet derived growth factor (PDGF) are found in early fracture hematoma, and these factors modulate cell proliferation and differentiation.
Bone morphogenetic protein and interleukin 1 and 6 are expressed during cartilage formation.
Correct Answer: Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1)
774. (2451) Q2-2916:
Which of the following molecules are present in a hematoma after a fracture and aid in modulating cell proliferation and differentiation:
1) Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1)
3) Interleukin-1 (IL-1)
2) Transforming growth factor-beta (TGF-B) and platelet derived growth factor (PDGF)
5) Vascular endothelial growth factor (VEGF)
4) Interleukin-6 (IL-6)
Important concepts to remember regarding signaling proteins include:
Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1) influence embryonic bone formation and fracture healing. Vascular endothelial growth factor (VEGF) plays a role in cartilage hypertrophy at the growth plate and during fracture healing.
Transforming growth factor-beta (TGF-B) and platelet derived growth factor (PDGF) are found in early fracture hematoma, and these factors modulate cell proliferation and differentiation.
Bone morphogenetic protein and interleukin 1 and 6 are expressed during cartilage formation. Correct Answer: Transforming growth factor-beta (TGF-B) and platelet derived growth factor (PDGF)
Which of the following molecules play an important role in cartilage hypertrophy during growth plate development and ossification in fracture healing:
1) Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1)
3) Interleukin-1 (IL-1)
2) Transforming growth factor-beta (TGF-B) and platelet derived growth factor (PDGF)
5) Vascular endothelial growth factor (VEGF)
4) Interleukin-6 (IL-6)
Important concepts to remember regarding signaling proteins include:
Indian hedgehog (IHH) and core binding factor alpha 1 (Cbfa1) influence embryonic bone formation and fracture healing. Vascular endothelial growth factor (VEGF) plays a role in cartilage hypertrophy at the growth plate and during fracture healing.
Transforming growth factor-beta (TGF-B) and platelet derived growth factor (PDGF) are found in early fracture hematoma, and these factors modulate cell proliferation and differentiation.
Bone morphogenetic protein and interleukin 1 and 6 are expressed during cartilage formation.
Correct Answer: Vascular endothelial growth factor (VEGF)
776. (2453) Q2-2918:
All of the following factors are important to achieve primary osteonal healing during plate fixation except:
1) Anatomic reduction
3) Adequate vascular supply
2) Rigid fixation
5) Very low strain levels
4) Moderate-to-high strain levels
In primary osteonal bone healing, osteoclasts cut channels across the bone contact sites and blood vessels, and osteoblasts fill in the gap with new bone.
To achieve osteonal healing, there must be an anatomic reduction with rigid fixation, an adequate blood supply, and the amount of motion at the fracture site must be very small to none (very low strain levels).
Moderate-to-high strain levels occur if there is motion at the osteosynthesis site. This motion results from poor fixation (lack of rigidity) or excessive loading during the healing period. High strain levels in the gap favor the formation of granulation tissue rather than bone.
Correct Answer: Moderate-to-high strain levels
777. (2454) Q2-2919:
All of the following factors increase the rigidity of an external fixator except:
1) Increased individual pin diameter
3) Increased bone-to-rod distance
2) Increased pin number
5) Separating half pins by 45°
4) Increased pin group separation
There are many factors that increase the rigidity of an external fixator, including: Increased pin diameter
Increased pin number Decreased bone-to-rod distance Increased pin group separation Separating half pins by 45°
Increasing the bone-to-rod distance decreases the rigidity of the system. The fracture gap is also important. The fracture gap should be minimized for excellent bone apposition.
Correct Answer: Increased bone-to-rod distance
Which of the following graft types has both osteoinductive and osteoconductive properties:
1) Autogenous bone marrow
3) Bone morphogenetic protein-2 (BMP-2)
2) Coral-based hydroxyapatite bone graft substitute
5) Cancellous bone graft
4) Recombinant bone morphogenetic protein-7 (rhBMP-7)
Grafting materials may include osteoconductive and/or osteoinductive properties and osteoprogenitor cells.
Cancellous bone and vascularized bone graft are the only materials that have significant osteoconductive, osteoinductive, and osteoprogenitor cells.
Several materials are mainly osteoinductive. Remember the definition of osteoinductive and osteoconductive properties:
Osteoinductive factors: Molecules that have the capability of inducing osteoblastic precursors to differentiate into mature bone forming cells.
Osteoinductive factors (without significant osteoconductive properties) include growth factors such as BMP-2 and rhBMP-7 (OP-1, Stryker Biotech, Hopkinton, Mass) and demineralized bone matrix.
Osteoconductive factors: The ability of a porous material to provide a scaffold for new bone formation.
Osteoconductive materials (without significant osteoinductive properties) include ceramics such as coral-based hydroxyapatite graft substitutes, Norian skeletal repair system (Norian Corporation, Cupertino, Calif), and calcium sulfate pellets (Osteoset, Wright Medical Technology Inc., Arlington, Tenn).
Bone marrow has the potential of supplying osteoprogenitor cells but has little osteoinductive or osteoconductive properties. Correct Answer: Cancellous bone graft
779. (2456) Q2-2921:
Which of the following materials has mainly osteoconductive properties with little or no osteoinductive ability:
1) Autogenous bone marrow
3) Bone morphogenetic protein-2 (BMP-2)
2) Coral-based hydroxyapatite bone graft substitute
5) Cancellous bone graft
4) Recombinant bone morphogenetic protein-7 (rhBMP-7)
Grafting materials may include osteoconductive and/or osteoinductive properties and osteoprogenitor cells.
Cancellous bone and vascularized bone graft are the only materials that have significant osteoconductive, osteoinductive, and osteoprogenitor cells.
Several materials are mainly osteoinductive. Remember the definition of osteoinductive and osteoconductive properties:
Osteoinductive factors: Molecules that have the capability of inducing osteoblastic precursors to differentiate into mature bone forming cells.
Osteoinductive factors (without significant osteoconductive properties) include growth factors such as BMP-2 and rhBMP-7 (OP-1, Stryker Biotech, Hopkinton, Mass) and demineralized bone matrix.
Osteoconductive factors: The ability of a porous material to provide a scaffold for new bone formation.
Osteoconductive materials (without significant osteoinductive properties) include ceramics such as coral-based hydroxyapatite graft substitutes, Norian skeletal repair system (Norian Corporation, Cupertino, Calif), and calcium sulfate pellets (Osteoset, Wright Medical Technology Inc., Arlington, Tenn).
Bone marrow has the potential of supplying osteoprogenitor cells but has little osteoinductive or osteoconductive properties. Correct Answer: Coral-based hydroxyapatite bone graft substitute
Which of the following materials has mainly osteoinductive properties with little or no osteoconductive ability:
1) Autogenous bone marrow
3) Calcium sulfate crystals
2) Coral-based hydroxyapatite bone graft substitute
5) Cancellous bone graft
4) Recombinant bone morphogenetic protein-7 (rhBMP-7)
Grafting materials may include osteoconductive and/or osteoinductive properties and osteoprogenitor cells.
Cancellous bone and vascularized bone graft are the only materials that have significant osteoconductive, osteoinductive, and osteoprogenitor cells.
Several materials are mainly osteoinductive. Remember the definition of osteoinductive and osteoconductive properties:
Osteoinductive factors: Molecules that have the capability of inducing osteoblastic precursors to differentiate into mature bone forming cells.
Osteoinductive factors (without significant osteoconductive properties) include growth factors such as BMP-2 and rhBMP-7 (OP-1, Stryker Biotech, Hopkinton, Mass) and demineralized bone matrix.
Osteoconductive factors: The ability of a porous material to provide a scaffold for new bone formation.
Osteoconductive materials (without significant osteoinductive properties) include ceramics such as coral-based hydroxyapatite graft substitutes, Norian skeletal repair system (Norian Corporation, Cupertino, Calif), and calcium sulfate pellets (Osteoset, Wright Medical Technology Inc., Arlington, Tenn).
Bone marrow has the potential of supplying osteoprogenitor cells but has little osteoinductive or osteoconductive properties. Correct Answer: Recombinant bone morphogenetic protein-7 (rhBMP-7)
Slide 1 Slide 2 Slide 3
A 65-year-old man has severe foot pain. His plain radiograph is shown in Slide 1, and a needle biopsy specimen in Slides and 3. The most likely diagnosis is:
1) Coccidioidomycosis
3) Rheumatoid arthritis
2) Pigmented villonodular synovitis
5) Tuberculosus
4) Gout
Gout is caused by the deposition of monosodium urate crystals in tissues, typically around joints. Common locations of gout include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first affected location is the great toe. Gout commonly occurs inside a joint for two reasons - synovial fluid is a poorer solvent than plasma and lower temperatures (as in peripheral joints) favor crystallization.
Neutrophils ingest the crystals and release potent lysosomal enzymes. Punched lesions may be seen on radiographs in chronic cases, and one can often see an overlying lip of cortex at the edge of the lesion.
Histologically, the tophi have several features:
Acellular amorphous material Macrophages
Foreign body giant cells
In this patient, the joint space is preserved on the plain radiographs. The biopsy specimen has the characteristic features of gout -acellular amorphous material, macrophages, and foreign body giant cells.
Correct Answer: Gout
Slide 1 Slide 2 Slide 3
A 65-year-old man has severe foot pain. His plain radiograph is shown in Slide 1, and a needle biopsy specimen in Slides 2 and
3. The most appropriate treatment for this patient is:
1) Irrigation/debridement followed by antibiotics
3) Diphosphonate therapy
2) Chemotherapy followed by wide resection
5) Arthroscopic debridement
4) Nonsteriodal anti-inflammatory agents
Gout is caused by the deposition of monosodium urate crystals in tissues, typically around joints. Common locations of gout include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first affected location is the great toe. Gout commonly occurs inside a joint for two reasons - synovial fluid is a poorer solvent than plasma and lower temperatures (as in peripheral joints) favor crystallization.
Neutrophils ingest the crystals and release potent lysosomal enzymes. Punched lesions may be seen on radiographs in chronic cases, and one can often see an overlying lip of cortex at the edge of the lesion.
Histologically, the tophi have several features:
Acellular amorphous material Macrophages
Foreign body giant cells
In this patient, the joint space is preserved on the plain radiographs. The biopsy specimen has the characteristic features of gout -acellular amorphous material, macrophages, and foreign body giant cells.
The treatment of gout includes nonsteroidal anti-inflammatory drugs and medications such as allopurinol and colchicines, which lower hyperuricemia.
Correct Answer: Nonsteriodal anti-inflammatory agents
Slide 1 Slide 2 Slide 3 Slide 4
A 60-year-old man has severe knee pain. His plain radiographs are shown in Slide 1. His T1- and T2-weighted sagittal magnetic resonance images (MRIs) are shown in Slides 2 and 3. A biopsy specimen is shown in Slide 4. The most likely diagnosis is:
1) Coccidioidomycosis
3) Rheumatoid arthritis
2) Pigmented villonodular synovitis
5) Tuberculosus
4) Gout
Gout is caused by the deposition of monosodium urate crystals in tissues, typically around joints. Common locations of gout include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first affected location is the great toe. Gout commonly occurs inside a joint for two reasons - synovial fluid is a poorer solvent than plasma and lower temperatures (as in peripheral joints) favor crystallization.
Neutrophils ingest the crystals and release potent lysosomal enzymes. Punched lesions may be seen on radiographs in chronic cases, and one can often see an overlying lip of cortex at the edge of the lesion.
Histologically, the tophi have several features:
Acellular amorphous material Macrophages
Foreign body giant cells
In this patient, the joint space is preserved on the plain radiographs. The MRI scans show periarticular erosions. The biopsy specimen has the characteristic features of gout - acellular amorphous material, macrophages, and foreign body giant cells.
Correct Answer: Gout

 

 

 

Slide 1 Slide 2 Slide 3 Slide 4

A 60-year-old man has severe knee pain. His plain radiographs are shown in Slide 1. His T1- and T2-weighted sagittal magnetic resonance images (MRIs) are shown in Slides 2 and 3. A biopsy specimen is shown in Slide 4. The most appropriate treatment for this patient is:

 

1) Irrigation/debridement followed by antibiotics

3) Diphosphonate therapy

2) Chemotherapy followed by wide resection

5) Arthroscopic debridement

4) Nonsteriodal anti-inflammatory agents

 

Gout is caused by the deposition of monosodium urate crystals in tissues, typically around joints. Common locations of gout include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first affected location is the great toe. Gout commonly occurs inside a joint for two reasons - synovial fluid is a poorer solvent than plasma and lower temperatures (as in peripheral joints) favor crystallization.

 

Neutrophils ingest the crystals and release potent lysosomal enzymes. Punched lesions may be seen on radiographs in chronic cases, and one can often see an overlying lip of cortex at the edge of the lesion.

Histologically, the tophi have several features:

 

 

Acellular amorphous material Macrophages

 

Foreign body giant cells

In this patient, the joint space is preserved on the plain radiographs. The biopsy specimen has the characteristic features of gout -acellular amorphous material, macrophages, and foreign body giant cells.

The treatment of gout includes nonsteroidal anti-inflammatory drugs and medications such as allopurinol and colchicines, which lower hyperuricemia.

Correct Answer: Nonsteriodal anti-inflammatory agents

 

 

Slide 1 Slide 2 Slide 3

A 55-year-old man has severe wrist pain with erythema and soft tissue swelling. The plain radiograph is shown in Slide 1 and a biopsy specimen is shown in Slide 2 and Slide 3. The most likely diagnosis is:

 

1) Septic arthritis

3) Gout

2) Osteomyelitis

5) Tuberculosis

4) Metastatic lung carcinoma

 

The plain radiographs show a destructive lesion in the wrist in the distal radius and at the scaphotrapezial joint. The joint spaces are preserved. The histology shows the features of gout: acellular amorphous tissue, macrophages, and giant cells.

Gout is caused by the deposition of monosodium urate crystals in tissues typically around joints. Common locations include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first attack is in the great toe. Gout commonly occurs inside a joint for two reasons:

 

 

The synovial fluid is a poorer solvent than plasma

 

Lower temperatures (as in peripheral joints) favor crystallization

Neutrophils ingest the crystals and then release potent lysosomal enzymes. Punched lesions may be seen on radiographs in chronic cases. One can often see an overlying lip of cortex at the edge of the lesion.

Histologically, the tophi have several features:

 

 

Acellular amorphous material Macrophages

 

 

Foreign body giant cells Correct Answer: Gout

 

Slide 1 Slide 2 Slide 3

A 55-year-old man has severe wrist pain with erythema and soft tissue swelling. The plain radiograph is shown in Slide 1 and a biopsy specimen is shown in Slide 2 and Slide 3. Which of the following would be the best treatment:

 

1) Debridement and antibiotics

3) External beam irradiation

2) Nonsteroidal anti-inflammatory medications

5) Thumb basal joint arthroplasty

4) Wide resection and wrist fusion

 

The plain radiographs show a destructive lesion in the wrist in the distal radius and at the scaphotrapezial joint. The joint spaces are preserved. The histology shows the features of gout: acellular amorphous tissue, macrophages, and giant cells.

Gout is caused by the deposition of monosodium urate crystals in tissues typically around joints. Common locations include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first attack is in the great toe. Gout commonly occurs inside a joint for two reasons:

 

 

The synovial fluid is a poorer solvent than plasma

 

Lower temperatures (as in peripheral joints) favor crystallization

 

Neutrophils ingest the crystals and then release potent lysosomal enzymes. Histologically, the tophi have several features: Acellular amorphous material

 

Macrophages

 

Foreign body giant cells

 

The first line of treatment is nonsteroidal anti-inflammatory medications. Correct Answer: Nonsteroidal anti-inflammatory medications

 

787. (2573) Q2-3046:

Which of the following statements is true regarding gout:

 

1) Gout is more common in females than males.

3) Gout is very common in heart transplant patients on cyclosporine.

2) Urate overproduction is the most common cause.

5) Joint space destruction is an early radiographic finding.

4) The serum uric acid level is always elevated in an acute attack.

 

Gout is caused by the deposition of monosodium urate crystals in tissues typically around joints. Common locations include the great toe, heel, ankle, and knee. In approximately 50% of patients, the first attack is in the great toe. Gout commonly occurs inside a joint for two reasons:

 

 

The synovial fluid is a poorer solvent than plasma

 

Lower temperatures (as in peripheral joints) favor crystallization One should remember the following:

 

 

Gout is much more common in males (ratio of 20:1). An inability to excrete uric acid is the primary cause.

 

 

Gout is very common in transplant patients taking cyclosporine. Serum uric acid level is often normal in an acute attack.

 

Joint space is usually preserved on plain radiographs (early disease).

Correct Answer: Gout is very common in heart transplant patients on cyclosporine.

 

 

 

 

 

Slide 1 Slide 2

A 9-year-old boy has a history of multiple fractures. He presents with left leg pain following a minor fall. His anteroposterior (Slide 1) and lateral (Slide 2) plain radiographs are shown. Which of the following is the most likely diagnosis:

 

1) Child abuse

3) Osteopetrosis

2) Osteomalacia (rickets)

5) Leukemia

4) Osteogenesis imperfecta

 

The anteroposterior and lateral radiographs show thinned cortices and a gentle S-shaped curve of the tibia. The overall alignment of the tibia, as well as the physes, is normal. These are the radiographic features of osteogenesis imperfecta.

Child abuse, osteomalacia (rickets), osteopetrosis, and leukemia must be distinguished from osteogenesis imperfecta. In child abuse, multiple fractures are at different stages of healing. Osteomalacia has widened physes and osteopetrosis has marked bone sclerosis and absence of a medullary cavity. Patients with leukemia have lytic destructive lesions.

 

In osteogenesis imperfecta, the genetic defect involves type I collagen. Type I collagen is made up of two alpha-1 chains and one alpha-2 chain in a triple helix. Glycine is the smallest amino acid and is crucial for coiling of the triple helix. Mutations in the glycine chain lead to severe forms of osteogenesis imperfecta.

 

One should also remember the Silence classification:

 

Type

Inheritance

Sclera

Severity

I

AD

Blue

Mild form, normal teeth

II

AR

Blue

Lethal form, die early

III

AR

Normal

Severe, progressively deforming

IV

AD

Normal

Moderately severe

 

 

Biphosphonate therapy can be used to slow bone remodeling and increase bone mass. Correct Answer: Osteogenesis imperfecta

 

Slide 1 Slide 2

A 9-year-old boy has a history of multiple fractures. He presents with left leg pain following a minor fall. His anteroposterior (Slide 1) and lateral (Slide 2) plain radiographs are shown. The most likely genetic defect would be:

 

1) FGF receptor 3

3) Cartilage oligomeric matrix protein

2) Type I collagen

5) Type II collagen

4) Fibrillin

 

The anteroposterior and lateral radiographs show thinned cortices and a gentle S-shaped curve of the tibia. The overall alignment of the tibia, as well as the physes, is normal. These are the radiographic features of osteogenesis imperfecta.

In osteogenesis imperfecta, the genetic defect involves type I collagen. Type I collagen is made up of two alpha-1 chains and one alpha-2 chain in a triple helix. Glycine is the smallest amino acid and is crucial for coiling of the triple helix. Mutations in the glycine chain lead to severe forms of osteogenesis imperfecta.

 

One should also remember the Silence classification:

 

Type

Inheritance

Sclera

Severity

I

AD

Blue

Mild form, normal teeth

II

AR

Blue

Lethal form, die early

III

AR

Normal

Severe, progressively deforming

IV

AD

Normal

Moderately severe

 

Biphosphonate therapy can be used to slow bone remodeling and increase bone mass. With regard to the incorrect choices:

 

 

FGF receptor 3 is associated with achondroplasia. Fibrillin is associated with Marfan's syndrome.

 

Type II collagen is associated with spondyloepiphyseal dsyplasia.

 

Cartilage oligomeric matrix protein is associated with pseudoachondroplasia.

Correct Answer: Type I collagen

 

 

Slide 1 Slide 2

A 9-year-old boy has a history of multiple fractures. He presents with left leg pain following a minor fall. His anteroposterior (Slide 1) and lateral (Slide 2) plain radiographs are shown. Which of the following can be an effective pharmacologic treatment:

 

1) Diphosphonate therapy

3) Cytotoxic multi-agent chemotherapy

2) Vitamin D and calcium

5) Growth hormone

4) Systemic antibiotics

 

The anteroposterior and lateral radiographs show thinned cortices and a gentle S-shaped curve of the tibia. The overall alignment of the tibia, as well as the physes, is normal. These are the radiographic features of osteogenesis imperfecta.

In osteogenesis imperfecta, the genetic defect involves type I collagen. Type I collagen is made up of two alpha-1 chains and one alpha-2 chain in a triple helix. Glycine is the smallest amino acid and is crucial for coiling of the triple helix. Mutations in the glycine chain lead to severe forms of osteogenesis imperfecta.

 

One should also remember the Silence classification:

 

Type

Inheritance

Sclera

Severity

I

AD

Blue

Mild form, normal teeth

II

AR

Blue

Lethal form, die early

III

AR

Normal

Severe, progressively deforming

IV

AD

Normal

Moderately severe

 

 

Biphosphonate therapy can be used to slow bone remodeling and increase bone mass. Correct Answer: Diphosphonate therapy

 

Slide 1 Slide 2

A 9-year-old boy has a history of multiple fractures. He presents with left leg pain following a minor fall. He has blue sclerae and normal dentition. His anteroposterior (Slide 1) and lateral (Slide 2) plain radiographs are shown. Which of the following is the most likely mode of inheritance of this condition:

 

1) Autosomal recessive

3) X-linked dominant

2) Autosomal dominant

5) Sporadic mutation, no mendelian pattern

4) X-linked recessive

 

The anteroposterior and lateral radiographs show thinned cortices and a gentle S-shaped curve of the tibia. The overall alignment of the tibia, as well as the physes, is normal. These are the radiographic features of osteogenesis imperfecta.

In osteogenesis imperfecta, the genetic defect involves type I collagen. Type I collagen is made up of two alpha-1 chains and one alpha-2 chain in a triple helix. Glycine is the smallest amino acid and is crucial for coiling of the triple helix. Mutations in the glycine chain lead to severe forms of osteogenesis imperfecta.

 

With the blue sclerae and normal dentition, the patient most likely has Silence type I osteogenesis imperfecta, which has an autosomal dominant inheritance pattern.

One should also remember the Silence classification:

 

Type

Inheritance

Sclera

Severity

I

AD

Blue

Mild form, normal teeth

II

AR

Blue

Lethal form, die early

III

AR

Normal

Severe, progressively deforming

IV

AD

Normal

Moderately severe

 

 

Biphosphonate therapy can be used to slow bone remodeling and increase bone mass. Correct Answer: Autosomal dominant

 

792. (2666) Q2-3159:

Which of the following statements is true concerning the use of intra-articular steroids in the treatment of osteoarthritis of the knee in randomized trials:

 

1) Intra-articular steroids showed no benefit over placebo.

3) Intra-articular steroids were better than placebo at 12 weeks.

2) Intra-articular steroids were better than placebo at 1 to 3 weeks.

5) Intra-articular steroids were less beneficial than placebo at 12 weeks.

4) Intra-articular steroids were less beneficial than placebo at 1 to 3 weeks.

 

Intra-articular corticosteroid treatment is commonly used in patients with osteoarthritis of the knee.

Randomized trials have shown a significant benefit of corticosteroid injection over placebo at 1 to 3 weeks (in various studies). Using pain as an outcome measure, the benefit is not significant when studied at 6 to 12 weeks.

Correct Answer: Intra-articular steroids were better than placebo at 1 to 3 weeks.

 

Which of the following is the most common complication after performing an intra-articular corticosteroid injection in a patient with arthritis:

 

1) Transient increase in pain

3) Skin depigmentation

2) Infection

5) Flushing and agitation

4) Skin and fat atrophy

 

A transient increase in pain is the most common complication following an intra-articular injection. The increase in pain is called a flare. The flare usually resolves within 24 hours. The less soluble steroid compounds may precipitate flares more commonly than the more soluble types.

 

Complications from intra-articular steroid injections are:

  1. Transient increase in pain (most common)

    1. In approximately 5%

    2. Subsides within 24 hours

    3. May be caused by the less soluble steroids

  2. Skin and subcutaneous tissue atrophy

  3. Depigmentation

  4. Systemic effects (fairly common)

    1. Usually mild and resolve quickly

    2. Flushing, slight agitation

    3. May worsen glucose control in patients with diabetes

  5. Adrenal suppression (when given more than 1 to 2 times per month)

     

  6. Infection occurs in 1 in 10,000 patients Correct Answer: Transient increase in pain

 

Slide 1

An 80-year-old man has left hip pain with ambulation. A plain radiograph is shown (Slide). The most likely process is:

 

1) Benign bone neoplasm

3) Metabolic bone disorder

2) Malignant bone neoplasm

5) Bacterial infection

4) Metastatic bone disease

 

 

Plain radiographs are the mainstay of diagnosis for Pagetâs disease. Radiographic features include: Enlargement and expansion of the bone

 

 

Coarsened trabeculae Cortical thickening

 

Lucent and sclerotic changes

Notice on this radiograph that there are coarsened trabeculae and bone deformities. A sharp delineation between the cortex and medullary cavity is not present. The cortices have been remodeled, and a small stress fracture in the lateral cortex of the subtrochanteric level is apparent.

 

This patient has Pagetâs disease, which is a metabolic bone disorder.

Technetium bone scans are sensitive to sites of involvement. Generally, at the time of diagnosis, there is no change in the number of the involved bones.

The serum alkaline phosphatase level is elevated in approximately 95% of patients. Urinary markers of bone turnovers are elevated and include hydroxyproline, N-telopeptide, and deoxypyridinoline.

 

Bone biopsy is seldom required to make the diagnosis of Pagetâs disease. Correct Answer: Metabolic bone disorder

 

Slide 1

An 80-year-old man has left hip pain with ambulation. A plain radiograph is shown (Slide). The cause of this process is most likely:

 

1) Primary bone malignancy

3) Viral infection

2) Bacterial infection

5) Genetic disorder involving type 1 collagen

4) Vascular insult

 

Notice on this radiograph that there are coarsened trabeculae and bone deformities. A sharp delineation between the cortex and medullary cavity is not present. The cortices have been remodeled, and a small stress fracture in the lateral cortex of the subtrochanteric level is apparent.

 

This patient has Pagetâs disease, which is a metabolic bone disorder.

Infection with a paramyxovirus has been implicated in Pagetâs disease. Inclusions that resemble viral nucleocapsid have been found with electron microscopy in the nuclei and cytoplasm of osteoclasts in Pagetâs disease. Controversy exists whether the virus belongs to the measles, canine distemper, or respiratory syncytial viruses.

 

 

 

 

Correct Answer: Viral infection 796. (2705) Q2-3200:

 

Slide 1

An 80-year-old man has left hip pain with ambulation. A plain radiograph is shown (Slide). Which of the following describes the probable inheritance pattern:

 

1) Autosomal recessive

3) X-linked recessive

2) Austosomal dominant

5) No genetic associations

4) X-linked dominant

 

Notice on this radiograph that there are coarsened trabeculae and bone deformities. A sharp delineation between the cortex and medullary cavity is not present. The cortices have been remodeled, and a small stress fracture in the lateral cortex of the subtrochanteric level is apparent.

 

This patient has Pagetâs disease, which is a metabolic bone disorder.

The inheritance pattern of Pagetâs disease is most likely autosomal dominant in pattern. One should remember that a first-degree relative has a seven times greater chance of developing Pagetâs disease than the general population. The exact inheritance is not known although the HLA locus and chromosome 18q (10,11) have been implicated.

 

Correct Answer: Austosomal dominant

 

 

 

 

 

Slide 1

An 80-year-old man has left hip pain with ambulation. A plain radiograph is shown (Slide). Which of the following would not be expected to be elevated in this patient:

 

1) Urinary total hydroxyproline

3) Serum calcium

2) Serum alkaline phosphatase

5) Urinary deoxypyridinoline

4) Urinary N-telopeptide

 

Notice on this radiograph that there are coarsened trabeculae and bone deformities. A sharp delineation between the cortex and medullary cavity is not present. The cortices have been remodeled, and a small stress fracture in the lateral cortex of the subtrochanteric level is apparent.

 

This patient has Pagetâs disease, which is a metabolic bone disorder.

In Pagetâs disease, serum and urinary markers reflect the rate of increased bone turnover â bone resorption and bone formation. Elevated in active disease:

 

Serum alkaline phosphatase

 

 

Serum bone-specific alkaline phosphatase Urinary hydroxyproline

 

 

Urinary N-telopeptide of collagen Urinary deoxypyridinoline

Note that the serum calcium level is usually normal in Pagetâs disease. However, if a patient is immobilized and has active and extensive Pagetâs disease, then the serum calcium level may become elevated.

Correct Answer: Serum calcium

 

 

 

 

 

Slide 1

An 80-year-old man has left hip pain with ambulation. A plain radiograph is shown (Slide). Which of the following can be used to treat this disorder:

 

1) Antiviral agents

3) Interferon alpha

2) Prolonged antibiotic therapy

5) Low-dose cytotoxic chemotherapy

4) Biphosphonates

 

Notice on this radiograph that there are coarsened trabeculae and bone deformities. A sharp delineation between the cortex and medullary cavity is not present. The cortices have been remodeled, and a small stress fracture in the lateral cortex of the subtrochanteric level is apparent.

 

This patient has Pagetâs disease, which is a metabolic bone disorder.

Biphosphonate therapy has become the mainstay of treatment. Biphosphonates poison the osteoclast by disturbing the ruffled border. Bone resorption is halted, and the markers of collagen breakdown in the urine markedly diminish.

Correct Answer: Biphosphonates

 

 

799. (2716) Q2-3211:

Which of the following articular cartilage collagens regulates type II collagen fibril diameter:

 

1) Type I

3) Type V

2) Type III

5) Type XI

4) Type IX

 

The three types of collagen in articular cartilage are:

  1. Type II

    1. 90% to 95% of the total collagen

    2. Highly cross-linked and interconnected

  2. Type IX

    1. Forms cross-links with type II

  3. Type XI

     

    1. Regulates the type II fibril diameter Correct Answer: Type XI

Which of the following statements concerning type II collagen in articular cartilage is false:

 

1) Type II collagen comprises 90% to 95% of the articular cartilage.

3) Type IX collagen regulates the type II fiber diameter.

2) The fibers are arranged parallel to the surface in the superficial or tangential zone.

5) The fibers are oriented in a perpendicular fashion in the deep or basal zone.

4) Normally, the collagen turnover is very slow.

 

The three types of collagen in articular cartilage are:

  1. Type II

    1. 90% to 95% of the total collagen

    2. Highly cross-linked and interconnected

  2. Type IX

    1. Forms cross-links with type II

  3. Type XI

    1. Regulates the type II fibril diameter In articular cartilage organization:

Cartilage layer Superficial or tangential Intermediate or transitional Deep or basal

Collagen fiber arrangement Parallel to the surface

Oblique to the surface Perpendicular to the surface

In normal states, the collagen turnover is slow. In contrast, collagen and proteoglycan turnover can be rapid in disease states (such as septic arthritis).

Correct Answer: Type IX collagen regulates the type II fiber diameter.

 

 

801. (2718) Q2-3213:

Which of the following articular cartilage collagens forms cross-links with type II collagen:

 

1) Type I

3) Type V

2) Type III

5) Type XI

4) Type IX

 

The three types of collagen in articular cartilage are:

  1. Type II

    1. 90% to 95% of the total collagen

    2. Highly cross-linked and interconnected

  2. Type IX

    1. Forms cross-links with type II

  3. Type XI

     

    1. Regulates the type II fibril diameter Correct Answer: Type IX

Which of the following factors has a chondroprotective (anabolic) function:

 

1) Transforming growth factor beta

3) Interleukin-1

2) Matrix metalloproteinases

5) Cyclooxygenase (COX-2)

4) Tumor necrosis factor alpha

 

I. Cartilage Metabolism and Regulation

  1. Nutrition through diffusion (low oxygen tension, 1% to 2%)

  2. Energy through glycolysis

  3. Transforming growth factor beta (TGF-B)

    1. Chondroprotective effect

    2. Smad3 which is transcription factor activated by TGF-B also is chondroprotective

  4. Insulin-like growth factor increases collagen and proteoglycan synthesis

  5. Bone morphogenetic protein (BMP)-2 and BMP-7 increase proteoglycan synthesis and maintain chondrocyte phenotype

  6. Interleukin-1

    1. Inhibits proteoglycan synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  7. Tumor necrosis factor alpha

    1. Inhibits collagen synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  8. Other catabolic enzymes

    1. Cyclooxygenase (COX-2)

    2. Nitric oxide synthetase

Chondroprotective (anabolic) TGF-B

Smad3

Insulin-like growth factor BMP-2

BMP-7

Chondro-ablative (catabolic) Interleukin-1

Tumor necrosis factor alpha COX-2

Nitric oxide synthetase

 

Correct Answer: Transforming growth factor beta

 

 

 

1) Bone morphogenetic protein (BMP)-2

3) Transforming growth factor beta

2) BMP-7

5) Smad3

4) Tumor necrosis factor alpha

 

I. Cartilage Metabolism and Regulation

  1. Nutrition through diffusion (low oxygen tension, 1% to 2%)

  2. Energy through glycolysis

  3. Transforming growth factor beta (TGF-B)

    1. Chondroprotective effect

    2. Smad3 which is transcription factor activated by TGF-B also is chondroprotective

  4. Insulin-like growth factor increases collagen and proteoglycan synthesis

  5. Bone morphogenetic protein (BMP)-2 and BMP-7 increase proteoglycan synthesis and maintain chondrocyte phenotype

  6. Interleukin-1

    1. Inhibits proteoglycan synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  7. Tumor necrosis factor alpha

    1. Inhibits collagen synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  8. Other catabolic enzymes

    1. Cyclooxygenase (COX-2)

    2. Nitric oxide synthetase

Chondroprotective (anabolic) TGF-B

Smad3

Insulin-like growth factor BMP-2

BMP-7

Chondro-ablative (catabolic) Interleukin-1

Tumor necrosis factor alpha COX-2

Nitric oxide synthetase Metalloproteinase

 

Correct Answer: Tumor necrosis factor alpha

 

 

 

1) Bone morphogenetic protein (BMP)-2

3) Matrix metalloproteinases

2) BMP-7

5) Insulin-like growth factor 1

4) Transforming growth factor beta

 

I. Cartilage Metabolism and Regulation

  1. Nutrition through diffusion (low oxygen tension, 1% to 2%)

  2. Energy through glycolysis

  3. Transforming growth factor beta (TGF-B)

    1. Chondroprotective effect

    2. Smad3 which is transcription factor activated by TGF-B also is chondroprotective

  4. Insulin-like growth factor increases collagen and proteoglycan synthesis

  5. Bone morphogenetic protein (BMP)-2 and BMP-7 increase proteoglycan synthesis and maintain chondrocyte phenotype

  6. Interleukin-1

    1. Inhibits proteoglycan synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  7. Tumor necrosis factor alpha

    1. Inhibits collagen synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  8. Other catabolic enzymes

    1. Cyclooxygenase (COX-2)

    2. Nitric oxide synthetase

Chondroprotective (anabolic) TGF-B

Smad3

Insulin-like growth factor BMP-2

BMP-7

Chondro-ablative (catabolic) Interleukin-1

Tumor necrosis factor alpha COX-2

Nitric oxide synthetase Metalloproteinase

 

Correct Answer: Matrix metalloproteinases

 

 

 

1) Bone morphogenetic protein (BMP)-2

3) Smad3

2) BMP-7

5) Cyclooxygenase (COX-2)

4) Insulin-like growth factor 1

 

I. Cartilage Metabolism and Regulation

  1. Nutrition through diffusion (low oxygen tension, 1% to 2%)

  2. Energy through glycolysis

  3. Transforming growth factor beta (TGF-B)

    1. Chondroprotective effect

    2. Smad3 which is transcription factor activated by TGF-B also is chondroprotective

  4. Insulin-like growth factor increases collagen and proteoglycan synthesis

  5. Bone morphogenetic protein (BMP)-2 and BMP-7 increase proteoglycan synthesis and maintain chondrocyte phenotype

  6. Interleukin-1

    1. Inhibits proteoglycan synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  7. Tumor necrosis factor alpha

    1. Inhibits collagen synthesis

    2. Stimulates metalloproteinase activity (catabolic enzymes)

  8. Other catabolic enzymes

    1. Cyclooxygenase (COX-2)

    2. Nitric oxide synthetase

Chondroprotective (anabolic) TGF-B

Smad3

Insulin-like growth factor BMP-2

BMP-7

Chondro-ablative (catabolic) Interleukin-1

Tumor necrosis factor alpha COX-2

Nitric oxide synthetase Metalloproteinase

 

Correct Answer: Cyclooxygenase (COX-2)

 

 

806. (2723) Q2-3218:

Which of the following muscle groups comprises the mobile wad of the forearm:

 

1) Brachioradialis, extensor carpi radialis longus, extensor carpi radialis brevisq

3) Brachioradialis, extensor carpi radialis brevis, extensor pollicis brevis

2) Brachioradialis, extensor pollicis brevis, extensor digitorum communis

5) Extensor carpi ulnaris, extensor pollicis brevis, extensor digitorum communis

4) Brachioradialis, extensor carpi radialis brevis, extensor digitorum communis

 

The forearm contains the anterior, dorsal, and mobile wad. The following muscles are located in each compartment:

Mobile wad

 

Brachioradialis

 

 

Extensor carpi radialis brevis Extensor carpi radialis longus

Volar compartment

 

Flexor carpi ulnaris

 

 

 

Flexor digitorum profundus Flexor digitorum superficialis Palmaris longus

 

 

Flexor carpi radialis Flexor pollicis longus

Correct Answer: Brachioradialis, extensor carpi radialis longus, extensor carpi radialis brevisq

 

 

 

1) Posterior tibialis

3) Medial gastrocnemius

2) Flexor hallucis longus

5) Flexor digitorum longus

4) Soleus

 

Of the four compartments, the deep posterior compartment is the most difficult to release. The surgeon must release the soleus muscle from the tibia to decompress the deep posterior compartment.

The tibialis posterior muscle often has its own fascial sheath in the deep posterior compartment. When a surgeon releases the deep posterior compartment, this fascial sheath (if present) should be released.

Correct Answer: Soleus

 

 

808. (2725) Q2-3220:

Which of the following leg muscles often has its own fascial envelope (separate compartment):

 

1) Anterior tibialis muscle

3) Peroneus longus muscle

2) Posterior tibialis muscle

5) Flexor hallucis longus muscle

4) Flexor digitorum longus muscle

 

Of the four compartments, the deep posterior compartment is the most difficult to release. The surgeon must release the soleus muscle from the tibia to decompress the deep posterior compartment.

The tibialis posterior muscle often has its own fascial sheath in the deep posterior compartment. When a surgeon releases the deep posterior compartment, this fascial sheath (if present) should be released.

Correct Answer: Posterior tibialis muscle

 

 

809. (2726) Q2-3221:

In patients with a tibia fracture, which of the following compartments are most prone to develop a compartment syndrome:

 

1) Anterior and lateral

3) Lateral and superficial posterior

2) Anterior and deep posterior

5) Superficial and deep posterior

4) Lateral and deep posterior

 

In a study by Heckman and colleagues, the level of the fracture site is the region with the highest tissue pressure. This was found to be true in all four components. The highest pressures are located in the anterior and deep posterior components.Correct Answer: Anterior and deep posterior

 

 

 

1) 1% to 2%

3) 10% to 20%

2) 5% to 10%

5) 30% to 40%

4) 20% to 30%

 

Compartment syndromes occur in approximately 5% to 10% of tibia fractures. Patients with tibia fractures have the highest risk of all fracture patients.

 

Adult fracture patients at risk for compartment syndrome include (in descending order): Tibia shaft fractures

 

Femoral shaft fractures

 

 

Both bone forearm fractures Distal radius fractures

 

Children with fractures who are at risk include (in descending order): Tibial shaft fractures

 

 

Supracondylar humerus fractures Both bone forearm fractures

Correct Answer: 5% to 10%

 

 

811. (2728) Q2-3223:

In patients with a closed tibia fracture and suspected compartment syndrome, the region of the leg that will most likely have the highest tissue pressure measurement is:

 

1) The middle of the leg

3) At the level of the fracture

2) 5 cm proximal to the fracture site

5) The proximal one-third of the leg

4) 5 cm distal to the fracture site

 

In a study by Heckman and colleagues, the level of the fracture site is the region with the highest tissue pressure. This was found to be true in all four components. The highest pressures are located in the anterior and deep posterior components.

Correct Answer: At the level of the fracture

 

 

812. (2729) Q2-3224:

Which of the following may be beneficial in decreasing the deleterious effects of total muscle ischemia in a patient who has a compartment syndrome:

 

1) Systemic steroids

3) Elevation of the extremity above the heart

2) Hypothermia

5) Anticoagulant therapy

4) Antihypertensive therapy

 

Aside from performing a fasciotomy, little can be done for patients with a compartment syndrome. Hypothermia, systemic corticosteroids, and anticoagulation therapy may increase muscle tolerance to ischemia.

Steroids and anticoagulation are not reasonable options because there is an impaired blood supply to the muscle (ie, these agents cannot enter the muscle). Hypothermia can be used to gain some time if immediate fasciotomy cannot be performed.

Correct Answer: Hypothermia

 

and nerve ischemia occurs:

 

1) Paresthesia

3) Pain on passive stretch of muscle

2) Loss of peripheral pulses

5) Loss of motor function

4) Delayed capillary refill

 

Compartment syndromes are difficult to diagnose. It is important to diagnosis compartment syndrome before irreversible muscle and nerve damage occurs.

Pain out of proportion to the injury and pain with passive stretch are the most important subjective and objective findings before a compartment syndrome has fully developed. Pain will subside after a prolonged period of ischemia. The muscle and nerves in the compartment are no longer viable, and the pain will diminish.

 

Correct Answer: Pain on passive stretch of muscle

 

 

814. (2731) Q2-3226:

Which of the following is the normal resting pressure in skeletal muscle:

 

1) 0 mm Hg to 8 mm Hg

3) 18 mm Hg to 24 mm Hg

2) 10 mm Hg to 16 mm Hg

5) 30 mm Hg to 36 mm Hg

4) 24 mm Hg to 30 mm Hg

 

Normal resting muscle tissue pressure is between 0 mm Hg and 8 mm Hg. Remember, if one squeezes the muscle or pushes on it, then the compartment pressure increases.

Normal tissues have adequate tissue perfusion with increases in compartment pressure to within 10 mm Hg of the diastolic pressure. In damaged tissue (eg, tibia fracture), perfusion can be impaired when the diastolic pressure reaches within 20 mm Hg of the diastolic pressure.

 

 

One should remember that hypotensive patients with extremity injuries are prone to compartment syndromes. Correct Answer: 0 mm Hg to 8 mm Hg

 

815. (2732) Q2-3227:

In injured tissues, ischemia begins when the tissue pressure within the compartment comes within       mm Hg of the diastolic pressure.

 

1) 10

3) 30

2) 20

5) 50

4) 40

 

Normal tissues have adequate tissue perfusion with increases in compartment pressure to within 10 mm Hg of the diastolic pressure. In damaged tissue (eg, tibia fracture), perfusion can be impaired when the diastolic pressure reaches within 20 mm Hg of the diastolic pressure.

 

 

One should remember that hypotensive patients with extremity injuries are prone to compartment syndromes. Correct Answer: 20

 

 

1) 1 to 2 hours

3) 4 to 6 hours

2) 2 to 4 hours

5) 8 to 10 hours

4) 6 to 8 hours

 

Loss of nerve electrical conduction begins after 2 hours of complete ischemia. Peripheral nerves can tolerate up to 4 hours of complete ischemia. A neurapraxic (loss of conduction capability) injury usually recovers. After 8 hours of complete ischemia, nerves cannot recover.

 

Patients will lose the sense of pain in a compartment with total ischemia after 2 to 8 hours because there is no conduction to the nerve. One can expect little recovery once this painless state has occurred.

Correct Answer: 8 to 10 hours

 

 

817. (2734) Q2-3230:

Complete muscle ischemia that leads to irreversible muscle damage occurs after which of the following time periods:

 

1) 1 to 2 hours

3) 4 to 6 hours

2) 2 to 4 hours

5) 8 to 10 hours

4) 6 to 8 hours

 

Skeletal muscle tolerates periods of complete muscle ischemia for 3 to 4 hours without irreversible damage. Variable recovery occurs with ischemia for 6 to 8 hours. When the period of ischemia is more than 8 hours, there is irreversible muscle damage. After 8 hours, the muscle cells degenerate and, grossly, the muscle contracts as the muscle cells are replaced with scar tissue and contracture may result.

 

 

Remember to let a tourniquet down after 2 hours of ischemia. One does not want to enter the tolerance period of 3 to 4 hours. Correct Answer: 8 to 10 hours

 

818. (2735) Q2-3231:

Skeletal muscle may remain viable (electrically responsive) following a period of total ischemia. Which of the following is the correct time interval for the tolerance to total muscle ischemia (complete recovery can be expected):

 

1) 3 to 4 hours

3) 6 to 8 hours

2) 4 to 6 hours

5) 10 to 12 hours

4) 8 to 10 hours

 

Skeletal muscle tolerates periods of complete muscle ischemia for 3 to 4 hours without irreversible damage. Variable recovery occurs with ischemia for 6 to 8 hours. When the period of ischemia is more than 8 hours, there is irreversible muscle damage. After 8 hours, the muscle cells degenerate and, grossly, the muscle contracts as the muscle cells are replaced with scar tissue and contracture may result.

 

 

Remember to let a tourniquet down after 2 hours of ischemia. One does not want to enter the tolerance period of 3 to 4 hours. Correct Answer: 3 to 4 hours

 

 

1) The pullout strength of a locked unicortical screw is only 30% of a standard bicortical screw.

3) Locked bicortical screws have greater toggle than standard bicortical screws.

2) Toggle between the screws and plate is greater than standard plating.

5) Locked plating is biomechanically similar to external fixation with a lower moment arm.

4) Friction between the plate and cortical bone is greater in locked plating compared to standard plating.

 

Locking plates have become a popular, effective method of stabilizing metaphyseal/epiphyseal fractures with comminution and short articular fragments.

 

Important biomechanical features of locking plates include1 :

 

Locked screws can function as individual blade plates in the distal fragment.

 

 

Locking plates can effectively serve as bridge plates, providing excellent fixation in short distal articular fragments. Compression of the plate against the bone is less than that of conventional plating, resulting in less devascularization of the underlying cortex.

 

There is no toggling between the locked screws and the plate.

 

 

The pullout strength of a locked unicortical screw is approximately 60% of a standard bicortical screw. Locking plates are similar biomechanically to an external fixator.

 

Moment arms are less because the plate is closer to the bone's neutral axis than the connecting bar of the external fixator.

Correct Answer: Locked plating is biomechanically similar to external fixation with a lower moment arm.

 

 

820. (2780) Q2-3278:

Which of the following statements concerning locking plates is true:

 

1) The pullout strength of a locked unicortical screw is only 60% of a standard bicortical screw.

3) Locked bicortical screws have greater toggle than standard bicortical screws.

2) Toggle between the screws and plate is greater than standard plating.

5) Locked plating is not biomechanically similar to external fixation with a lower moment arm.

4) Friction between the plate and cortical bone is greater in locked plating compared to standard plating.

 

Locking plates have become a popular and effective method of stabilizing metaphyseal/epiphyseal fractures with comminution and short articular fragments.

Important biomechanical features of locking plates include:

 

 

locked screws can function as individual blade plates in the distal fragment locking plates can effective serve as bridge plates

 

excellent fixation in short distal articular fragments

 

 

compression of the plate against the bone is less than that of conventional plating less devascularization of the underlying cortex

 

there is no toggling between the locked screws and the plate

 

pullout strength of a locked unicortical screw is approximately 60% a standard bicortical screw

 

locking plates are similar biomechanically to an external fixator moment arms are less because the plate is closer to the bone's neutral axis than the connecting bar of the external fixator

Correct Answer: The pullout strength of a locked unicortical screw is only 60% of a standard bicortical screw.

 

 

 

1) Autosomal dominant inheritance

3) Sex-linked dominant

2) Autosomal recessive inheritance

5) Sporadic

4) Sex-linked recessive

 

Hemophilia A is transmitted by a sex-linked recessive inheritance pattern. Important points to remember:

 

 

Hemophilia A (classic hemophilia) Factor VIII deficiency

 

 

Sex-linked recessive trait Incidence - 1/5000 live male births

 

 

25% of cases are sporadic (no family history) Hemophilia B (Christmas disease)

 

Factor IX deficiency

 

Sex-linked recessive trait

 

 

Incidence - 1/30,000 live male births Correct Answer: Sex-linked recessive

 

822. (2782) Q2-3280:

Which of the following is the most important pathophysiology factor in hemophilic arthropathy:

 

1) Viral joint infection

3) Hemosiderin depositionq

2) Bacterial joint infection

5) Neuropathic damage

4) Subchondral bone microfractures

 

Hemosiderin deposition leads to synovial hypertrophy, bone erosions, recurrent bleeding, and eventual destruction of the articular surfaces and arthrofibrosis.

 

 

Synovial A cells (surface layer phagocytic cells) ingest hemosiderin Mixed inflammatory cell population

 

 

 

Lymphocytes Plasma cells Histiocytes

 

 

Leads to bone erosion from the thickened synovium Correct Answer: Hemosiderin depositionq

 

823. (2965) Q2-3471:

The âbystander effectâ in cancer gene therapy is:

 

1) Resistance to gene therapy by neighbor tumor cells after irradiation.

3) The death of neighbor untargeted tumor cells during cell-targeted suicide.

2) The secretion of tumor suppressor cytokines by neighbor cells.

5) None of the above.

4) Anaphylaxis-like side effects seen during tumor gene therapy.

 

The âbystander effectâ is the death of neighbor untargeted tumor cells during cell-targeted suicide, whereby HSV thymine kinase gene targeted cells commit suicide by absorbing gancyclovir, a prodrug that is turned intracellularly into a toxic metabolite by the targeting gene through phosphorylation.Correct Answer: The death of neighbor untargeted tumor cells during cell-targeted suicide.

 

 

 

1) Type X collagen

3) Cartilage oligomeric protein

2) Carbonic anhydrase type II, proton pump

5) Core binding factor alpha 1 (Cbfa1)

4) Fibrillin

 

The defect in cleidocranial dysplasia involves Cbfa1.

 

Cbfa1 is a transcription factor (coded by the Cbfa1 gene) that is necessary and sufficient for differentiation of cells into osteoblasts and facilitates chondrocyte differentiation during enchondral bone formation.

The other responses refer to:

 

 

 

 

Metaphyseal chondrodysplasia (Schmid type): Type X collagen Osteopetrosis: Carbonic anhydrase type II, proton pump Metaphyseal epiphyseal dysplasia: Cartilage oligomeric protein Marfan's syndrome: Fibrillin

 

Correct Answer: Core binding factor alpha 1 (Cbfa1)

 

 

825. (2992) Q2-3498:

Which of the following is associated with achondroplasia:

 

1) Type X collagen

3) Fibrillin

2) Sulfate transporter gene

5) Type I collagen (Col 1A1, 1A2)

4) Fibroblast growth factor 3 (FGF-3) (receptor)

 

Achondroplasia is caused by a defect in FGF-3 receptor, resulting in an inhibition of chondrocyte proliferation in the proliferative zone of the physis. One possible theory is that this mutation results in a receptor that is active even without binding of the fibroblast growth factor ligand, thereby causing an overactive receptor. This is a gain of function mutation (Dietz).

 

The other responses refer to:

 

 

Metaphyseal chondrodysplasia (Schmid type): Type X collagen Diastrophic dysplasia: Sulfate transporter gene

 

 

Osteogenesis imperfecta: Type I collagen (Col 1A1, 1A2) Marfanâs syndrome: Fibrillin

Correct Answer: Fibroblast growth factor 3 (FGF-3) (receptor)

 

 

 

1) Type X collagen

3) Beta glucosidase

2) Sulfate transporter gene

5) Carbonic anhydrase type II, proton pump

4) Galpha S (GNAS1)

 

Pseudohypoparathyroidism (PHP) (Albright Hereditary Osteodystrophy [AHO]) - end organ insensitivity; in AHO, germline mutation that leads to loss of function of Galpha S (GNAS1); causes end-organ resistance to PTH (Zaleske).

  1. PHP - short stature, short metacarpals (4th and 5th), rounded facies

    1. Mental retardation, tetany

    2. Sex-linked dominant

  2. Laboratory features

    1. Hypocalcemia

    2. Hyperphopshatemia

    3. Normal PTH

  3. Other features

The other responses refer to:

 

 

Metaphyseal chondrodysplasia (Schmid type): Type X collagen Diastrophic dysplasia: Sulfate transporter gene

 

Gaucher's disease: Beta glucosidase

 

 

Osteopetrosis: Carbonic anhydrase type II, proton pump Correct Answer: Galpha S (GNAS1)

 

827. (2994) Q2-3500:

Which of the following is associated with Marfan's syndrome:

 

1) Sulfate transporter gene

3) Carbonic anhydrase type II, proton pump

2) Fibroblast growth factor 3 (FGF-3) (receptor)

5) Fibrillin

4) Core binding factor alpha 1 (Cbfa1)

 

The defective gene (located on chromosome 15) in Marfan's syndrome encodes for fibrillin. Fibrillin is a structural component of elastin and contains microfibrils (Dietz).

Features of Marfan's syndrome include:

 

 

 

Long, thin limbs (dolichostenomelia) Pectus excavatum, carinatum Scoliosis

 

 

High and narrow palate Ectopia lentis

 

 

Dilation of the ascending aorta Dural ectasia

 

The other responses refer to: Achondroplasia: FGF-3 receptor

 

 

Diastrophic dysplasia: Sulfate transporter gene Cleidocranial dysplasia: Cbfa1

 

 

Osteopetrosis: Carbonic anhydrase type II, proton pump Correct Answer: Fibrillin

 

 

1) Receptor activator of nuclear factor-kB (RANK)

3) Bone morphogenetic protein-7

2) Osteoprotegerin

5) Parathyroid hormone related protein (PTHrP)

4) Core binding factor alpha 1 (Cbfa1)

 

Four proteins that regulate osteoclast activation have been discovered:

  1. RANK binds to a receptor on osteoclast precursor cells and positively effects their final differentiation into osteoclasts.

  2. Osteoprotegerin is a soluble decoy receptor that resembles RANK and inhibits osteoclasts.

  3. Tumor necrosis factor-related activation induced cytokine (TRANCE)

  4. Osteoclast differentiation factor Note:

 

Cbfa1 is a transcription factor (coded by the Cbfa1 gene) that is necessary and sufficient for differentiation of cells into osteoblasts and facilitates chondrocyte differentiation during enchondral bone formation.

Correct Answer: Receptor activator of nuclear factor-kB (RANK)

 

 

829. (3004) Q2-3510:

Which of the following proteins negatively affects osteoclast precursor cells:

 

1) Receptor activator of nuclear factor-kB (RANK)

3) Bone morphogenetic protein-7

2) Osteoprotegerin

5) Parathyroid hormone related protein (PTHrP)

4) Core binding factor alpha 1 (Cbfa1)

 

Four proteins that regulate osteoclast activation have been discovered:

  1. RANK binds to a receptor on osteoclast precursor cells and positively effects their final differentiation into osteoclasts.

  2. Osteoprotegerin is a soluble decoy receptor that resembles RANK and inhibits osteoclasts.

  3. Tumor necrosis factor-related activation induced cytokine (TRANCE)

  4. Osteoclast differentiation factor Note:

 

Cbfa1 is a transcription factor (coded by the Cbfa1 gene) that is necessary and sufficient for differentiation of cells into osteoblasts and facilitates chondrocyte differentiation during enchondral bone formation.

Correct Answer: Osteoprotegerin

 

 

830. (3005) Q2-3511:

Which of the following proteins or genes is necessary for bone formation and induces osteocalcin:

 

1) Sox-9 gene

3) Tumor necrosis factor-related activation induced cytokine

2) Receptor activator of nuclear factor-kB protein

5) Core binding factor alpha 1 (Cbfa1) gene

  1. Osteoprotegerin

     

    Core binding factor alpha 1 (Cbfa1) and its gene (Cbfa1) have been described as anabolic regulators of bone. Cbfa1 is a transcription factor and is responsible for the differentiation of precursor cells into osteoblasts. It also enhances differentiation of chondrocytes during enchondral bone formation. When there is deficiency of Cbfa1, there can be abnormal bone development as in cleidocranial dysplasia.

     

    Correct Answer: Core binding factor alpha 1 (Cbfa1) gene

     

     

     

    1) 1,000

    3) 10,000

    2) 5,000

  2. 100,000

4) 30,000

 

The human genome is composed of 30,000 unique genes. Each gene is composed of a promotor or regulator region, and a transcriptional or coding region. Regulatory proteins or transcription factors bind to the promoter region of the gene to signal the beginning of transcription of the DNA into RNA or repress the expression of the gene. The coding region contains both introns and exons. Exon sequences of the gene directly code for the proteins, and the introns are spacers. The intron sequences are enzymatically removed from the newly transcribed messenger RNA by a splicing mechanism.

 

Correct Answer: 30,000

 

 

832. (3007) Q2-3513:

Which of the following portions of a gene directly codes for the messenger RNA for eventual translation into proteins on the ribosome:

 

1) Promoter region

3) Exon

2) Intron

5) Activator or repressor binding site

4) Coding region

 

The human genome is composed of 30,000 unique genes. Each gene is composed of a promotor or regulator region, and a transcriptional or coding region. Regulatory proteins or transcription factors bind to the promoter region of the gene to signal the beginning of transcription of the DNA into RNA or repress the expression of the gene. The coding region contains both introns and exons. Exon sequences of the gene directly code for the proteins, and the introns are spacers. The intron sequences are enzymatically removed from the newly transcribed messenger RNA by a splicing mechanism.

 

Correct Answer: Exon

 

 

833. (3008) Q2-3514:

Which of the following describes the inheritance pattern of achondroplasia:

 

1) X-linked recessive

3) Autosomal dominant

2) Sporadic

5) X-linked dominant

4) Autosomal recessive

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-dominant conditions: Achondroplasia

 

 

 

Spondyloepiphyseal dysplasia Multiple epiphyseal dysplasia Marfan's syndrome

 

 

 

 

Ehlers-Danlos syndrome Osteogenesis imperfecta (I, IV) Multiple hereditary exostosis Polydactyly

 

Correct Answer: Autosomal dominant

 

 

 

1) Autosomal recessive

3) X-linked recessive

2) Autosomal dominant

5) Sporadic

4) X-linked dominant

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-dominant conditions: Achondroplasia

 

 

 

Spondyloepiphyseal dysplasia Multiple epiphyseal dysplasia Marfan's syndrome

 

 

 

 

Ehlers-Danlos syndrome Osteogenesis imperfecta (I, IV) Multiple hereditary exostosis Polydactyly

 

Correct Answer: Autosomal dominant

 

 

835. (3010) Q2-3516:

Which of the following describes the inheritance pattern of Ehlers-Danlos syndrome:

 

1) Autosomal recessive

3) X-linked recessive

2) Autosomal dominant

5) Sporadic

4) X-linked dominant

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-dominant conditions: Achondroplasia

 

 

 

Spondyloepiphyseal dysplasia Multiple epiphyseal dysplasia Marfan's syndrome

 

 

 

 

Ehlers-Danlos syndrome Osteogenesis imperfecta (I, IV) Multiple hereditary exostosis Polydactyly

 

Correct Answer: Autosomal dominant

 

 

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-dominant conditions: Achondroplasia

 

 

 

Spondyloepiphyseal dysplasia Multiple epiphyseal dysplasia Marfan's syndrome

 

 

 

 

Ehlers-Danlos syndrome Osteogenesis imperfecta (I, IV) Multiple hereditary exostosis Polydactyly

 

Correct Answer: Autosomal dominant

 

 

837. (3012) Q2-3518:

Which of the following describes the inheritance pattern of polydactyly:

 

1) Autosomal recessive

3) X-linked recessive

2) Autosomal dominant

5) Sporadic

4) X-linked dominant

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-dominant conditions: Achondroplasia

 

 

 

Spondyloepiphyseal dysplasia Multiple epiphyseal dysplasia Marfan's syndrome

 

 

 

 

Ehlers-Danlos syndrome Osteogenesis imperfecta (I, IV) Multiple hereditary exostosis Polydactyly

 

Correct Answer: Autosomal dominant

 

 

 

1) Austosomal dominant

3) X-linked dominant

2) Austosomal recessive

5) Sporadic

4) X-linked recessive

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-recessive conditions: Sickle cell disease

 

 

Osteogenesis imperfecta (Types II, III) Hypophosphatasia

 

 

Homocystinuria Gaucher's disease

Correct Answer: Austosomal recessive

 

 

839. (3014) Q2-3520:

Which of the following describes the inheritance pattern of sickle cell disease:

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-recessive conditions: Sickle cell disease

 

 

Osteogenesis imperfecta (Types II, III) Hypophosphatasia

 

 

Homocystinuria Gaucher's disease

Correct Answer: Autosomal recessive

 

 

840. (3015) Q2-3521:

Which of the following describes the inheritance pattern of Gaucher's disease:

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-recessive conditions: Sickle cell disease

 

 

Osteogenesis imperfecta (Types II, III) Hypophosphatasia

 

 

Homocystinuria Gaucher's disease

Correct Answer: Autosomal recessive

 

 

841. (3016) Q2-3522:

Which of the following describes the inheritance pattern of homocystinuria:

 

1) Autosomal recessive

3) X-linked recessive

2) Autosomal dominant

5) Sporadic

4) X-linked dominant

 

Structural defects are usually transmitted by an autosomal-dominant pattern. In contrast, with metabolic or enzyme deficiencies, the condition is usually transmitted in an autosomal-recessive pattern.

 

Remember the major autosomal-recessive conditions: Sickle cell disease

 

 

Osteogenesis imperfecta (Types II, III) Hypophosphatasia

 

 

Homocystinuria Gaucher's disease

Correct Answer: Autosomal recessive

 

 

842. (3017) Q2-3523:

Which of the following describes the inheritance pattern for hypophosphatemic rickets:

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Common inheritance patterns that should be known for examinations:

 

Autosomal dominant

Autosomal recessive

X-linked dominant

X-linked recessive

Achondroplasia

Sickle cell

Hypophosphatemic rickets

Hemophilia (A, B)

SED (congenital)

OI (II, III)

 

Duchennes muscular dystrophy

MED

Hypophosphatasia

 

Hunters syndrome

Marfanâs syndrome

Homocystinuria

 

SED (tarda)

Ehlers-Danlos syndrome

Gaucherâs disease

 

Beckerâs muscular dystrophy

Abbreviations: OI (I,IV)=Osteogenesis imperfecta, SED=Spondyloepiphyseal dysplasia, MED=Multiple epiphyseal dysplasia, MHE=Multiple hereditary exostosis

Correct Answer: X-linked dominant

 

 

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Common inheritance patterns are shown in the Table below:

 

Autosomal dominant

Autosomal recessive

X-linked dominant

X-linked recessive

Achondroplasia

Sickle cell

Hypophosphatemic rickets

Hemophilia (A, B)

SED (congenital)

OI (II, III)

 

Duchennes muscular dystrophy

MED

Hypophosphatasia

 

Hunters syndrome

Marfanâs syndrome

Homocystinuria

 

SED (tarda)

Ehlers-Danlos syndrome

Gaucherâs disease

 

Beckerâs muscular dystrophy

Abbreviations: OI (I,IV)=Osteogenesis imperfecta, SED=Spondyloepiphyseal dysplasia, MED=Multiple epiphyseal dysplasia, MHE=Multiple hereditary exostosis

Correct Answer: X-linked recessive

 

 

844. (3019) Q2-3525:

Which of the following describes the inheritance pattern of Duchennes muscular dystrophy:

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Common inheritance patterns that should be known for examinations:

 

Autosomal dominant

Autosomal recessive

X-linked dominant

X-linked recessive

Achondroplasia

Sickle cell

Hypophosphatemic rickets

Hemophilia (A, B)

SED (congenital)

OI (II, III)

 

Duchennes muscular dystrophy

MED

Hypophosphatasia

 

Hunters syndrome

Marfanâs syndrome

Homocystinuria

 

SED (tarda)

Ehlers-Danlos syndrome

Gaucherâs disease

 

Beckerâs muscular dystrophy

Abbreviations: OI (I,IV)=Osteogenesis imperfecta, SED=Spondyloepiphyseal dysplasia, MED=Multiple epiphyseal dysplasia, MHE=Multiple hereditary exostosis

Correct Answer: X-linked recessive

 

 

 

1) Autosomal dominant

3) X-linked dominant

2) Autosomal recessive

5) Sporadic

4) X-linked recessive

 

Common inheritance patterns that should be known for examinations:

 

Autosomal dominant

Autosomal recessive

X-linked dominant

X-linked recessive

Achondroplasia

Sickle cell

Hypophosphatemic rickets

Hemophilia (A, B)

SED (congenital)

OI (II, III)

 

Duchennes muscular dystrophy

MED

Hypophosphatasia

 

Hunters syndrome

Marfanâs syndrome

Homocystinuria

 

SED (tarda)

Ehlers-Danlos syndrome

Gaucherâs disease

 

Beckerâs muscular dystrophy

Abbreviations: OI (I,IV)=Osteogenesis imperfecta, SED=Spondyloepiphyseal dysplasia, MED=Multiple epiphyseal dysplasia, MHE=Multiple hereditary exostosis

Correct Answer: X-linked recessive

 

 

846. (3021) Q2-3527:

Which of the following conditions is transmitted by an X-linked dominant inheritance pattern:

 

1) Hemophilia A

3) Duchennes muscular dystrophy

2) Hypophosphatemic rickets

5) Hypophosphatasia

4) Achondroplasia

 

There is only one condition that must be remembered for examinations that is transmitted through an X-linked dominant pattern -hypophosphatemic rickets.

 

Remember: the conditions which are x-linked recessive Hemophilia A, B - X-linked recessive

 

 

 

Duchennes muscular dystrophy - X-linked recessive Achondroplasia - Autosomal dominant Hypophosphatasia - Autosomal recessive

 

Correct Answer: Hypophosphatemic rickets

 

 

 

1) Hemophilia A

3) Hypophosphatemic rickets

2) Achondroplasia

5) Hypophosphatasia

4) Duchennes muscular dystrophy

 

Achondroplasia has an autosomal-dominant pattern of inheritance. Structural problems are usually transmitted via autosomal-dominant pattern.

If an affected individual is married to an unaffected person, then the chance of transmission to the children is 50%. The other conditions have the following transmission pattern:

 

Hemophilia A, B - X-linked recessive

 

 

 

Duchennes muscular dystrophy - X-linked recessive Achondroplasia - Autosomal dominant Hypophosphatasia - Autosomal recessive

 

Correct Answer: Achondroplasia

 

 

848. (3023) Q2-3529:

A man with an autosomal-dominant condition married a woman without the condition. What is the probability that one of the offspring will be affected:

 

1) 0%

3) 50%

2) 25%

5) 100%

4) 75%

 

For autosomal dominant, if one parent is a heterozygote and the other is normal, then the risk of transmission is to 50% of the offspring. Because of the dominance of the allele, heterozygotes manifest the condition.

For autosomal recessive, parents are usually not affected because they are heterozygotes. The risk of transmission is to 25% of the offspring. The children must have both recessive alleles to be affected.

Correct Answer: 50%

 

 

849. (3024) Q2-3530:

A man with a single autosomal-recessive gene marries a woman who does not carry the recessive gene. The chance of one of the children expressing the phenotype of the recessive gene is:

 

1) 0%

3) 50%

2) 25%

5) 100%

4) 75%

 

For autosomal dominant, if one parent is a heterozygote and the other is normal, then the risk of transmission is to 50% of the offspring. Because of the dominance of the allele, heterozygotes manifest the condition.

For autosomal recessive, parents are usually not affected because they are heterozygotes. The risk of transmission is to 25% of the offspring. The children must have both recessive alleles to be affected.

Because only one parent contains the gene, none of the children will be affected, although 25% of the children will carry the recessive gene.

Correct Answer: 0%

 

the children carrying the recessive gene is:

 

1) 0%

3) 50%

2) 25%

5) 100%

4) 75%

 

For autosomal dominant, if one parent is a heterozygote and the other is normal, then the risk of transmission is to 50% of the offspring. Because of the dominance of the allele, heterozygotes manifest the condition.

For autosomal recessive, parents are usually not affected because they are heterozygotes. The risk of transmission is to 25% of the offspring. The children must have both recessive alleles to be affected.

Because only one parent contains the gene, none of the children will be affected, although 25% of the children will carry the recessive gene.

Correct Answer: 25%

 

 

851. (3026) Q2-3532:

A man has an X-linked dominant condition and marries a woman who does not carry the abnormal gene. Which of the following is true concerning the offspring:

 

1) 50% of the daughters will be affected

3) 50% of the sons will be affected

2) 100% of the daughters will be affected

5) 25% of the sons and daughters will be affected

4) 100% of the sons will be affected

 

With X-linked dominant, heterozygotes will have the condition. If a woman has this condition, then she will transmit it to 50% of her sons and daughters.

In contrast, affected men transmit the condition to all of his daughters (because the daughter gets his X chromosome), but to none of the sons because the son gets the Y chromosome.

With X-linked recessive, the patterns are different between women and men.

X-linked recessive woman: An X-linked woman with the recessive allele is a carrier, but she is not affected because the allele is recessive.

Carrier females (X-linked recessive) transmit the condition to 50% of her daughters (who become carriers) and 50% of her sons (the sons are affected because their only X chromosome has the recessive gene).

Correct Answer: 100% of the daughters will be affected

 

 

 

1) 25% of the offspring will be affected

3) 25% of the sons will be affected

2) 100% of the daughters will be affected

5) 50% of the offspring will be affected

4) 100% of the sons will be affected

 

With X-linked dominant, heterozygotes will have the condition. If a woman has this condition, then she will transmit it to 50% of her sons and daughters.

In contrast, affected men transmit the condition to all of his daughters (because the daughter gets his X chromosome), but to none of the sons because the son gets the Y chromosome.

With X-linked recessive, the patterns are different between women and men.

X-linked recessive woman: An X-linked woman with the recessive allele is a carrier, but she is not affected because the allele is recessive.

Carrier females (X-linked recessive) transmit the condition to 50% of her daughters (who become carriers) and 50% of her sons (the sons are affected because their only X chromosome has the recessive gene).

Correct Answer: 50% of the offspring will be affected

 

 

853. (3028) Q2-3535:

Which of the following are actions of parathyroid hormone (PTH):

 

1) Increases kidney absorption of calcium and increases kidney absorption of phosphate

3) Directly activates osteoclast precursor cells to differentiate into osteoclasts

2) Increases kidney absorption of calcium and decreases kidney absorption of phosphate

5) Causes increased production of calcium binding protein

4) Decreases 1 alpha hydroxylase activity in the kidney

 

Parathyroid hormone increases calcium reabsorption from the kidney tubular cells and inhibits the reabsorption of phosphate.

Remember that PTH signals the osteoblasts to release receptor activator of nuclear factor -kB ligand (RANKL), which causes osteoclast activation â this is an indirect action.

PTH actions:

 

Facilitates absorption of calcium in the gastrointestinal system

 

 

Increases 1,25 dihydroxy vitamin D in the kidney by stimulating 1 alpha hydroxylase Facilitates reabsorption of calcium from the distal tubular renal tubular cells

 

 

Calcium is reabsorbed in the proximal and distal tubules, but only distal tubule is PTH dependent Inhibits reabsorption of phosphate in the kidney

 

Stimulates release of calcium and phosphate from bone (indirectly)

 

 

Causes release of receptor activator of nuclear factor -kB ligand (RANKL) from the surface of the osteoblasts Correct Answer: Increases kidney absorption of calcium and decreases kidney absorption of phosphate

 

 

1) Osteoblasts, osteoclasts, and distal kidney nephron

3) Osteoclasts and osteoclast progenitor cells

2) Osteoblasts, osteoclasts, and gastrointestinal cells

5) Osteoclast progenitor cells

4) Osteoblasts and distal kidney nephron

 

PTH actions:

 

Facilitates absorption of calcium in the gastrointestinal system

 

 

Increases 1,25 dihydroxy vitamin D in the kidney by stimulating 1 alpha hydroxylase Facilitates reabsorption of calcium from the distal tubular renal tubular cells

 

 

Calcium is reabsorbed in the proximal and distal tubules, but only distal tubule is PTH dependent Inhibits reabsorption of phosphate in the kidney

 

Stimulates release of calcium and phosphate from bone (indirectly)

 

Causes release of receptor activator of nuclear factor -kB ligand (RANKL) from the surface of the osteoblasts

Parathyroid hormone exerts its affects through receptors on osteoblasts and kidney nephron cells. Parathyroid hormone effects on the gut are indirect through an increased synthesis of 1,25 dihydroxy vitamin D. Parathyroid hormone acts on osteoblasts to release RANKL, which then acts on the osteoclast progenitor cells to differentiate into osteoclasts.

 

Correct Answer: Osteoblasts and distal kidney nephron

 

 

855. (3030) Q2-3537:

Which of the following is an action of 1,25 dihydroxy vitamin D:

 

1) Increases synthesis of calcium binding protein

3) Increases bone resorption by directly signaling osteoclasts

2) Causes kidney tubule cells to absorb calcium

5) Causes kidney tubule cells to absorb phosphorus

4) Increases parathyroid hormone (PTH) production

 

Vitamin D acts on the intestinal to increase calcium absorption. Calcium binding protein synthesis is increased. Vitamin D is an intracellular messenger, acting through the nucleus.

Vitamin D actions:

 

 

Increase the efficiency of calcium absorption in the intestine (primarily duodenum) Increases synthesis of calcium binding protein (and others)

 

Increases passage of calcium through the cell membrane

 

Moves calcium through the cell cytoplasm and into the circulation

 

 

Increases bone resorption by telling the osteoblasts to release receptor activator of nuclear factor -kB ligand Osteoblasts have vitamin D receptors

 

 

Vitamin D receptors exert a negative feedback on 1,25 dihydroxy vitamin D production Decreases PTH production

Correct Answer: Increases synthesis of calcium binding protein

 

surface:

 

1) Osteoprotegerin

3) Insulin-like growth factor

2) Transforming growth factor beta

5) Calcitonin

4) Parathyroid hormone (PTH) receptor

 

Osteoclast progenitor cells are activated to transform into osteoclasts when the RANKL activates the RANK receptor. The following factors cause release of RANKL from the osteoblast:

 

PTH

 

 

 

1,25 dihydroxy vitamin D Interleukin 11 Prostaglandin E2

 

Correct Answer: Parathyroid hormone (PTH) receptor

 

 

857. (3032) Q2-3539:

Which of the following cause the release of receptor activator of nuclear factor -kB ligand (RANKL) from the osteoblast cell surface:

 

1) Calcitonin

3) Transforming growth factor B

2) 1,25 dihydroxy vitamin D

5) Tumor necrosis factor

4) Insulin-like growth factor

 

Osteoclast progenitor cells are activated to transform into osteoclasts when the RANKL activates the RANK receptor. The following factors cause release of RANKL from the osteoblast:

 

PTH

 

 

 

1,25 dihydroxy vitamin D Interleukin 11 Prostaglandin E2

 

Correct Answer: 1,25 dihydroxy vitamin D

 

 

858. (3033) Q2-3540:

Calcitonin has which of the following functions:

 

1) Inhibits the release of receptor activator of nuclear factor -kB ligand (RANKL) from the surface of osteoblasts

3) Causes osteoclasts to withdraw from the bone surface

2) Increases the release of osteoprotegerin from the surface of osteoblasts

5) Causes a decrease in conversion of 25 hydroxy vitamin D into 1,25 dihydroxy vitamin D

4) Causes a decrease in conversion of vitamin D into 25 hydroxy vitamin D

 

Calcitonin has 1 major action:

 

Inhibits osteoclastic bone resorption â the osteoclast shrinks and withdraws from the bone surface Calcitonin can be used in the following conditions:

 

 

Paget's disease Osteoporosis

 

Hypercalcemia of malignancy

 

Calcitonin is used less frequently today than in the past. Diphosphonate agents are the main therapeutic agents. Correct Answer: Causes osteoclasts to withdraw from the bone surface

859. (3034) Q2-3541:

Which of the following soft tissue tumors may cause tumor-induced osteomalacia:

 

1) Liposarcoma

3) Synovial sarcoma

2) Malignant fibrous histiocytoma

5) Atypical lipoma

4) Hemangiopericytoma

 

Tumor-induced osteomalacia can be caused by a small tumor of bone or soft tissue (phosphaturic tumor). Small tumors may not be detected.

I. General Features

  1. Presentation

    1. Chronic, vague symptoms - principally, bone pain

    2. Muscle weakness

    3. Fractures may occur

  2. Metabolic profile

    1. Hypophosphatemia

    2. Low reabsorption of phosphate from the kidney

    3. 1,25 dihydroxy vitamin D - low or normal

    4. 25 hydroxy vitamin D, 24,25 dihydroxy vitamin D - normal

  3. Tumor types

    1. Soft tissue

      1. Hemangiopericytoma

      2. Sclerosing angioma

      3. Benign angiofibroma

      4. Neurofibromatosis

  4. Pathophysiology

    1. A molecule that wastes phosphorus - phosphatonin

  5. Radiographic features

    1. Osteopenia

    2. Pseudofractures

    3. Coarsened trabeculae

    4. Soft tissue - a small, well-circumscribed soft tissue mass may be noted

  6. Treatment

    1. Oral phosphate

       

    2. 1,25 dihydroxy vitamin D Correct Answer: Hemangiopericytoma

 

 

1) Osteosarcoma

3) Osteoblastoma

2) Ewing's sarcoma

5) Malignant fibrous histiocytoma

4) Adamantinoma

 

Tumor-induced osteomalacia can be caused by a small tumor of bone or soft tissue (phosphaturic tumor). Small tumors may not be detected.

I. General Features

  1. Presentation

    1. Chronic, vague symptoms - principally, bone pain

    2. Muscle weakness

    3. Fractures may occur

  2. Metabolic profile

    1. Hypophosphatemia

    2. Low reabsorption of phosphate from the kidney

    3. 1,25 dihydroxy vitamin D - low or normal

    4. 25 hydroxy vitamin D, 24,25 dihydroxy vitamin D - normal

  3. Tumor types

    1. Bone

      1. Nonossifying fibroma

      2. Osteoblastoma

      3. Giant cell tumor

      4. Fibrous dysplasia

  4. Pathophysiology

    1. A molecule is produced by the tumor that wastes phosphorus - phosphatonin

  5. Radiographic features

    1. Osteopenia

    2. Pseudofractures

    3. Coarsened trabeculae

    4. Soft tissue - a small, well-circumscribed soft tissue mass may be noted

  6. Treatment

    1. Oral phosphate

       

    2. 1,25 dihydroxy vitamin D Correct Answer: Osteoblastoma

 

 

1) Low serum calcium, low serum phosphate

3) Normal serum calcium, low serum phosphate

2) Low serum calcium, high serum phosphate

5) High serum calcium, low serum phosphate

4) Normal serum calcium, high serum phosphate

 

I. General Features

  1. Presentation

    1. Chronic, vague symptoms - principally, bone pain

    2. Muscle weakness

    3. Fractures may occur

  2. Metabolic profile

    1. Hypophosphatemia

    2. Low reabsorption of phosphate from the kidney

    3. 1,25 dihydroxy vitamin D - low or normal

    4. 25 hydroxy vitamin D, 24,25 dihydroxy vitamin D - normal

  3. Pathophysiology

    1. A molecule is produced by the tumor that wastes phosphorus - phosphatonin

  4. Radiographic features

    1. Osteopenia

    2. Pseudofractures

    3. Coarsened trabeculae

    4. Soft tissue - a small, well-circumscribed soft tissue mass may be noted

  5. Treatment

    1. Oral phosphate

    2. 1,25 dihydroxy vitamin D

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

Correct Answer: Normal serum calcium, low serum phosphate 862. (3037) Q2-3544:

 

 

 

 

In a patient with metabolic bone disease, which of the above metabolic patterns is most likely vitamin D-deficient rickets:

 

1) Scenario 1

3) Scenario 3

2) Scenario 2

5) Scenario 5

4) Scenario 4

 

In patients with vitamin D-deficient rickets, a low amount of vitamin D is present in the diet. Because of a low calcium level in patients with vitamin D deficiency, patients develop secondary hyperparathyroidism.

The increased parathyroid hormone (PTH) causes increased absorption of calcium from the small intestine and decreased absorption of phosphorus from the kidney. Therefore, serum calcium is low or normal, serum phosphate is decreased, and PTH is high. Increased bone resorption occurs, and 25 hydroxy and 1,25 dihydroxy vitamin D are low.

 

 

Patients are treated with supplemental vitamin D in their diet. Correct Answer: Scenario 1

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

 

 

In a patient with metabolic bone disease, which of the above scenarios would be consistent with dietary phosphate deficiency:

 

1) Scenario 1

3) Scenario 3

2) Scenario 2

5) Scenario 5

4) Scenario 4

 

Dietary phosphate deficiency is rare. Patients have a normal serum calcium and parathyroid hormone level, and the vitamin D levels are also normal. Because of an insufficient amount of phosphate, normal bone mineralization does not occur.

 

Patients are treated with supplemental neutral phosphate. Correct Answer: Scenario 2

 

 

 

864. (3039) Q2-3546:

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

A patient has gastrointestinal surgery and develops osteomalacia (rickets). Which of the above scenarios would be the most likely metabolic panel:

 

1) Scenario 1

3) Scenario 3

2) Scenario 2

5) Scenario 5

4) Scenario 4

 

Patients who have gastrointestinal surgery or have gastrointestinal disease (eg, Crohn's disease) may develop osteomalacia. The metabolic parameters are similar to that seen with dietary vitamin D deficiency â a low calcium level and resulting hyperparathyroidism.

 

Calcium is poorly absorbed or a steatorrhea is present, which binds the calcium so that it cannot be well absorbed. Because of a low calcium level, patients develop secondary hyperparathyroidism.

The increased parathyroid hormone (PTH) causes increased absorption of calcium from the small intestine and decreased absorption of phosphorus from the kidney. Therefore, serum calcium is low or normal, serum phosphate is decreased, and PTH is high. Increased bone resorption occurs, and 25 hydroxy and 1,25 dihydroxy vitamin D are low.

 

Correct Answer: Scenario 1

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

 

 

 

A patient has phosphate diabetes (vitamin D-resistant rickets). Which of the above metabolic profiles would most likely result:

 

1) Scenario 1

3) Scenario 4

2) Scenario 3

5) Scenario 7

4) Scenario 6

 

Phosphate diabetes is a type of vitamin D-resistant rickets. Patients are unable to reabsorb phosphate in the kidney tubules. The serum phosphate level is low, and patients are unable to mineralize osteiod because of the low phosphate. Serum calcium, parathyroid hormone, and vitamin D levels are normal. Patients are treated with large amounts of neutral phosphate in the diet.

 

 

Patients are resistant to vitamin D because of their inability to reabsorb phosphate in the kidney tubules. Correct Answer: Scenario 3

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

 

 

Which of the above metabolic profiles occurs in a patient who had vitamin D-resistant rickets with the inability to produce adequate amounts of the 1,25 dihydroxy vitamin D:

 

1) Scenario 3

3) Scenario 5

2) Scenario 4

5) Scenario 7

4) Scenario 6

 

Vitamin D-resistant rickets may occur when there is an inability to convert 25 hydroxy vitamin D into 1,25 dihydroxy vitamin D.

Patients develop secondary hyperparathyroidism. A low serum calcium level causes an increased parathyroid hormone (PTH) level. Parathyroid hormone causes the kidneys not to reabsorb phosphorus, and the serum phosphate is low. The serum 1,25 dihydroxy vitamin D level is low.

 

The metabolic profile is:

 

Serum calcium Low Serum phosphate Low Serum PTH High

25 vitamin D Normal

1,25 vitamin D Very low

 

 

Treatment is by dietary 1,25 dihydroxy vitamin D. Correct Answer: Scenario 4

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

L

H

H

L

L

L

 

 

 

Which of the above metabolic profiles occurs in a patient with vitamin D-resistant rickets with end-organ insensitivity to 1,25 dihydroxy vitamin D:

 

1) Scenario 3

3) Scenario 5

2) Scenario 4

5) Scenario 7

4) Scenario 6

 

One form of vitamin D-resistant rickets is end-organ insensitivity to 1,25 dihydroxy vitamin D. The small intestine gastrointestinal cells are not able to respond to 1,25 dihydroxy vitamin D. The serum calcium is low, and patients develop secondary hyperparathyroidism - high serum parathyroid hormone (PTH). The high serum PTH causes the kidneys not to reabsorb phosphate so that the serum phosphate level is low.

 

The metabolic profile is:

 

Serum calcium Low Serum phosphate Low Serum PTH High

25 vitamin D Normal or high 1,25 vitamin D Normal or high

Treatment is difficult; some patients with mild involvement are treated with vitamin D, and patients with severe disease may require calcium infusions.

Correct Answer: Scenario 7

 

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

 

 

Which of the above metabolic profiles occurs in a patient with renal tubular acidosis:

 

1) Scenario 3

3) Scenario 5

2) Scenario 4

5) Scenario 7

4) Scenario 6

 

In patients with renal tubular acidosis, the kidney has to secrete a positive ion (Na, Ca) to balance the pH. The secretion of calcium ions results in ostomalacia or rickets as there is insufficient calcium to mineralize newly formed osteiod.

With low serum calcium levels, the serum parathyroid hormone (PTH) level increases, causing decreased reabsorption of phosphate. Vitamin levels are normal. Renal tubular acidosis is the only condition in which there is increased urinary excretion of calcium.

 

The metabolic profile is:

 

Serum calcium Low Serum phosphate Low Serum PTH High

25 vitamin D Normal

1,25 vitamin D Normal

Urinary Ca High

 

 

The treatment of renal tubular acidosis is to alkalinize the urine. Correct Answer: Scenario 6

 

 

Serum

Urine

 

Ca

P

AP

PTH

25 D

1,25 D

Ca

Scenario 1

L

L L L L L

L

H

H

L

L

L

Scenario 2

N

H

N

N

N

N

Scenario 3

N

N

N

N

N

N

Scenario 4

L

H

H

N

L

L

Scenario 5

L

H

H

N/H

N/H

L

Scenario 6

L

H

H

N

N

H

Scenario 7

L

H

H

H

L

L

L

 

 

 

Which of the above metabolic profiles occurs in a patient with renal osteodystrophy:

 

1) Scenario 1

3) Scenario 5

2) Scenario 3

5) Scenario 7

4) Scenario 6

 

In patients with renal osteodystrophy, the renal tubular cells are damaged, resulting in the retention of phosphate. The kidney cells are unable to produce 1,25 dihydroxy vitamin D. Because the serum calcium level is low, patients develop secondary hyperparathyroidism.

 

The metabolic profile is:

 

Serum calcium Low Serum phosphate High Serum PTH High

1,25 vitamin D Low

 

 

The treatment is correction of the hyperparathyroidism. Correct Answer: Scenario 7

Which of the following serum metabolic profiles describes a patient with hypophosphatasia:

 

1) Normal calcium, normal dihydroxy vitamin D, and low alkaline phosphatase

3) Low calcium, low dihydroxy vitamin D, and low alkaline phosphatase

2) Low calcium, normal dihydroxy vitamin D, and low alkaline phosphatase

5) High calcium, high dihydroxy vitamin D, and high alkaline phosphatase

4) High calcium, high dihydroxy vitamin D, and low alkaline phosphatase

 

Hypophosphatasia is the inability to synthesize alkaline phosphatase by the bone, leukocytes, kidney, and intestine

  1. Autosomal recessive

  2. High levels of phosphoethanolamine in the urine

  3. When severe (high mortality)

    1. Growth retardation, failure to thrive

    2. Irritability, fever, vomiting

  4. When mild

    1. Fractures

    2. Short stature

    3. Poor fracture healing

    4. Osteomalacia

  5. Radiographic features

    1. Osteopenia

    2. Cup-shaped deformities of the proximal long bones

  6. Histological features - unmineralized osteiod seams

  7. Laboratory features

    1. Low serum alkaline phosphatase

    2. Normal Ca, 1,25 dihydroxy vitamin D

  8. Cause - inability to mineralize osteiod because the absence of alkaline phosphatase

  9. Treatment - high doses of vitamin D

Correct Answer: Normal calcium, normal dihydroxy vitamin D, and low alkaline phosphatase

 

 

871. (3046) Q2-3553:

Which of the following inheritance patterns occurs in patients with hypophosphatasia:

 

1) Autosomal recessive

3) X-linked dominant

2) Autosomal dominant

5) Sporadic

4) X-linked recessive

 

Hypophosphatasia is the inability to synthesize alkaline phosphatase by the bone, leukocytes, kidney, and intestine

  1. Autosomal recessive

  2. High levels of phosphoethanolamine in the urine

  3. When severe (high mortality)

    1. Growth retardation, failure to thrive

    2. Irritability, fever, vomiting

  4. When mild

    1. Fractures

    2. Short stature

    3. Poor fracture healing

    4. Osteomalacia

  5. Radiographic features

    1. Osteopenia

    2. Cup-shaped deformities of the proximal long bones

  6. Histological features - unmineralized osteiod seams

  7. Laboratory features

    1. Low serum alkaline phosphatase

    2. Normal Ca, 1,25 dihydroxy vitamin D

  8. Cause - inability to mineralize osteiod because the absence of alkaline phosphatase

     

  9. Treatment - high doses of vitamin D Correct Answer: Autosomal recessive

Which of the following is the basic defect in patients with pseudohypoparathyroidism (Albright Hereditary Osteodystrophy [AHO]):

 

1) End-organ resistance to 1,25 dihydroxy vitamin D

3) Inability to reabsorb phosphate in the kidney

2) End-organ resistance to parathyroid hormone (PTH)

5) Inability to synthesize alkaline phosphatase

4) Inability to produce 1,25 dihydroxy vitamin D

 

Pseudohypoparathyroidism (AHO) - end-organ insensitivity; in AHO, germline mutation that leads to loss of function of Galpha S (GNAS1); causes end-organ resistance to PTH

  1. PHP - short stature, short metacarpals (4th and 5th), rounded facies

    1. Mental retardation, tetany

    2. Sex-linked dominant

  2. Laboratory features

    1. Hypocalcemia

    2. Hyperphopshatemia

    3. Normal PTH

Correct Answer: End-organ resistance to parathyroid hormone (PTH)

 

 

873. (3048) Q2-3555:

Which of the following is the mode of inheritance for pseudohypoparathyroidism (Albright Hereditary Osteodystrophy [AHO]):

 

1) Autosomal recessive

3) Sex-linked dominant

2) Autosomal dominant

5) Sporadic

4) Sex-linked recessive

 

Pseudohypoparathyroidism (AHO) - end-organ insensitivity; in AHO, germline mutation that leads to loss of function of Galpha S (GNAS1); causes end-organ resistance to PTH

  1. PHP - short stature, short metacarpals (4th and 5th), rounded facies

    1. Mental retardation, tetany

    2. Sex-linked dominant

  2. Laboratory features

    1. Hypocalcemia

    2. Hyperphopshatemia

    3. Normal PTH

Correct Answer: Sex-linked dominant

 

Which of the following is the defect in pseudohypoparathyroidism (Albright Hereditary Osteodystrophy [AHO]):

 

1) Cartilage oligometric matrix protein

3) Sulfate transport protein

2) Fibroblast growth factor receptor 3

5) Galpha S (GNAS1)

4) Type II collagen

 

Pseudohypoparathyroidism (AHO) - end-organ insensitivity; in AHO, germline mutation that leads to loss of function of Galpha S (GNAS1); causes end-organ resistance to PTH

  1. PHP - short stature, short metacarpals (4th and 5th), rounded facies

    1. Mental retardation, tetany

    2. Sex-linked dominant

  2. Laboratory features

    1. Hypocalcemia

    2. Hyperphopshatemia

    3. Normal PTH

The other responses are also important to know:

 

 

Cartilage oligometric matrix protein - pseudoachondroplasia Fibroblast growth factor receptor 3 - achondroplasia

 

 

Sulfate transport protein - diastrophic dysplasia Type II collagen - spondyloepiphyseal dysplasia

Correct Answer: Galpha S (GNAS1)

 

 

875. (3071) Q2-3579:

Which of the following methods reduce radiation exposure to a surgeon during fluoroscopic procedures:

 

1) Avoiding the inverted C-arm position

3) Limiting the use of the foot pedal for controlling the fluoroscopy unit

2) Avoiding collimation of the radiation beam

5) Increasing the amperage of each exposure

4) Always standing on the opposite side of the C-arm

 

One of the best ways to limit radiation exposure is to increase distance from the C-arm. Surgeons should always stand on the opposite side of the C-arm and remember the following methods for reducing radiation exposure:

 

 

Increase distance (doubling distance reduces exposure by a factor of 4) Inverted position of the C-arm (increases distance)

 

 

Shielding: 90% attenuated by 0.25-mm apron Collimation (reduces the size of the beam)

 

 

Foot pedal to control the fluoroscopy unit (decreases the amount of exposure) Correct Answer: Always standing on the opposite side of the C-arm

 

876. (3072) Q2-3580:

At which of the following distances can surgeons expect to have no radiation exposure from scatter from a fluoroscopy unit:

 

1) 6 in

3) 2 ft

2) 1 ft

5) 6 ft

4) 3 ft

 

Radiation exposure decreases by a factor of 4 when a surgeon doubles the distance from the radiation beam. No radiation exists 6 ft from a fluoroscopy unit.Correct Answer: 6 ft

 

Which of the following amounts of radiation is received from a chest radiograph:

 

1) 1 mrem

3) 25 mrem

2) 10 mrem

5) 1,000 mrem

4) 500 mrem

 

Surgeons should know the radiation doses from common diagnostic tests. Common radiation exposures:

 

 

 

Chest radiograph Hip radiograph

 

 

Hip computed tomography C-arm (in beam)

 

Mini C-arm (in beam)

25 mrem

500 mrem

1,000 mrem

1,200 mrem/min to 4,000 mrem/min

120 mrem/min to 400 mrem/min

 

Correct Answer: 25 mrem

 

 

878. (3074) Q2-3582:

Which of the following amounts of radiation is received from a hip radiograph:

 

1) 10 mrem

3) 100 mrem

2) 25 mrem

5) 1,000 mrem

4) 500 mrem

 

Surgeons should know the radiation doses from common diagnostic tests. Common radiation exposures:

 

 

 

Chest radiograph Hip radiograph

 

 

Hip computed tomography C-arm (in beam)

 

Mini C-arm (in beam)

25 mrem

500 mrem

1,000 mrem

1,200 mrem/min to 4,000 mrem/min

120 mrem/min to 400 mrem/min

 

Correct Answer: 500 mrem

 

 

879. (3075) Q2-3583:

Which of the following amounts of radiation are received from a computed tomography (CT) scan of the hip:

 

1) 25 mrem

3) 500 mrem

2) 100 mrem

5) 5,000 mrem

4) 1,000 mrem

 

Surgeons should know the radiation doses from common diagnostic tests. Common radiation exposures:

 

Chest radiograph 25 mrem

Hip radiograph 500 mrem Hip computed tomography 1,000 mrem

C-arm (in beam 1,200 mrem/min to 4,000 mrem/min

Mini C-arm (in beam 120 mrem/min to 400 mrem/min Correct Answer: 1,000 mrem

 

Which of the following amounts of radiation are the maximum annual exposures to the whole body, thyroid gland, and hands:

 

1) 1 rem, 15 rem, 25 rem

3) 5 rem, 60 rem, 100 rem

2) 2 rem, 30 rem, 50 rem

5) 20 rem, 100 rem, 200 rem

4) 10 rem, 75 rem, 150 rem

 

Surgeons should know the maximum annual exposures of radiation.

 

 

 

Total body dose Eye

 

 

 

Thyroid Skin, hands Fetus

 

Correct Answer: 2 rem, 30 rem, 50 rem

2 rem or 5 rem

15 rem

30 rem

50 rem

0.5 rem over a period of 9 months (<0.05 mrem per month)

 

 

 

881. (3077) Q2-3585:

Which of the following numbers is the approximate number of intramedullary nailings of the tibia or femur that can be performed safely in regard to the maximum allowable radiation dose from a C-arm unit:

 

1) 50

3) 200

2) 100

5) 400

4) 300

 

 

 

C- arm fluoroscopy units- 4,000 mrem/min in the beam 5 mrem/min at 2 ft: scatter

 

1 mrem/min at 4 ft: scatter

 

 

Distances for which no radiation is expected Scatter: 0.1%, 3 ft from beam

0.025%, 6 ft from beam

 

 

Intramedullary nailing 100 mrem/nailing to127 mrem/nailing Translates to 394 nailings per year for safe exposure

 

Intramedullary nailing (femur, tibia)

 

 

 

Average exposure: 100 mrem/operation Average exposure (hands): 127 mrem/operation Tolerance:

 

 

Hands: Approximately 400 patients per year Thyroid gland: 1,960 patients per year

 

Important points

 

 

Placing pedicle screws results in the highest radiation exposure. Surgeons should avoid placing their hands directly in the radiation beam.

Correct Answer: 400

 

Which of the following statements is true concerning anterior cruciate ligament (ACL) tears in children with open physes:

 

1) The pattern of ACL failure is the same as adults.

3) The Lachmanâs test is seldom positive.

2) Associated meniscal tears are uncommon.

5) The pivot shift test is seldom positive.

4) The tear often occurs at the tibial insertion.

 

Although ACL injuries are less common in children than adults, this knee injury is becoming more common as children are involved in more athletic activities. Important points to remember include:

 

 

In children, the ACL collagen fibers extend from the ligament to epiphyseal cartilage. Many ACL injuries occur at the tibial insertion.

 

 

Tibial eminence avulsion fractures often accompany ACL injury. Associated meniscal injuries are common.

 

 

The physical examination findings are the same as in adults. Bicycle accidents are a common mechanism of injury.

Correct Answer: The tear often occurs at the tibial insertion.

 

 

883. (3262) Q2-4090:

Which of the following is found during differentiation of chondrocytes and the formation of the cartilage anlagen during enchondral growth:

 

1) CBAF1/RUNX2

3) Osterix

2) Vascular endothelial factor alpha (VEGF-A)

5) Receptor activator of nuclear factor-kB ligand (RANKL)

4) Low level of beta-catenin

 

Low levels of beta-catenin cause the mesenchyme to differentiate into cartilage (upregulation of SOX9). The chondrocytes develop organelles and produce cartilage specific collagens, types II, IX, and XI. The cartilage anlagen grows by interstitial and appositional growth, taking the shape of normal bones (epiphysis, metaphysis, and diaphysis).

 

Different processes and signals occur when the diaphysis ossifies. The cartilage cells stop growing and they hypertrophy. The chondrocytes express CBAF1/RUNX2 and VEGF-A. These factors attract blood vessels, osteoblasts, cartilage, and bone resorbing cells. The primary ossification center is then formed. The cartilage is removed, and the bone forms. At the surface of the diaphysis, the mesenchymal cells become osteoblasts and form bone.

 

Correct Answer: Low level of beta-catenin

 

 

884. (3263) Q2-4091:

Which of the following is found during the process of forming the primary ossification center (transition from primary cartilage anlagen to bone):

 

1) SOX9

3) Low levels of beta-catenin

2) Osteoprotegerin (OPG)

5) Receptor activator of nuclear factor-kB ligand (RANKL)

4) High levels of beta-catenin

 

Low levels of beta-catenin cause the mesenchyme to differentiate into cartilage (up-regulation of SOX9). The chondrocytes develop organelles and produce cartilage specific collagens, types II, IX, and XI. The cartilage anlagen grows by interstitial and appositional growth, taking the shape of normal bones (epiphysis, metaphysis, and diaphysis).

 

Different processes and signals occur when the diaphysis ossifies. The cartilage cells stop growing and they hypertrophy. High levels of beta-catenin induce this process (involves Wnt signaling and up-regulation of beta-catenin). The chondrocytes express CBAF1/RUNX2 and VEGF-A. These factors attract blood vessels, osteoblasts, cartilage, and bone resorbing cells. The primary ossification center is then formed. The cartilage is removed, and the bone forms. At the surface of the diaphysis, the mesenchymal cells become osteoblasts and form bone.

 

Correct Answer: High levels of beta-catenin

 

885. (3264) Q2-4101:

Which of the following occurs with myopathies:

 

1) Focal demyelination

3) High amplitude-long duration motor unit potentials

2) Nerve conduction velocity slowing

5) Specific conduction block sites

4) Small amplitude-short duration motor unit potentials

 

With focal nerve compression, focal demyelination is present. The axon remains intact but, with myelin loss, slowing of conduction occurs and a conduction block is possible.

 

Common findings with focal nerve compression include: Focal demyelination

 

 

 

Nerve conduction velocity slowing Conduction block across the site Fibrillation potentials

 

Positive sharp waves

 

High amplitude-long duration motor unit potentials (chronic denervation)

 

In contrast, small amplitude-short duration motor unit potentials are found in myopathy. Correct Answer: Small amplitude-short duration motor unit potentials

 

886. (3265) Q2-4103:

Which of the following is typically found with electrodiagnostic testing in neurogenic lesions:

 

1) Complex repetitive discharges

3) Myotonic discharges

2) Myokymic potentials

5) Fibrillations

4) Positive sharp waves

 

With electrodiagnostic testing, a clinician may find several characteristic features in different disorders: Denervation

 

Fibrillation

 

 

Positive sharp waves Fasciculations

Neurogenic lesions

 

 

Fasciculations Myokymic potentials

Myopathies

 

 

Complex repetitive discharges Myotonic discharges

Correct Answer: Myokymic potentials

 

Which of the following is typically found with electrodiagnostic testing in myopathies:

 

1) Positive sharp waves and fibrillations

3) Complex repetitive discharges and myotonic discharges

2) Positive sharp waves

5) Myokymic potentials

4) Fasciculations and myokymic potentials

 

With electrodiagnostic testing, a clinician may find several characteristic features in different disorders: Denervation

 

Fibrillation

 

 

Positive sharp waves Fasciculations

Neurogenic lesions

 

 

Fasciculations Myokymic potentials

Myopathies

 

 

Complex repetitive discharges Myotonic discharges

Correct Answer: Complex repetitive discharges and myotonic discharges

 

 

888. (3267) Q2-4106:

Fasciculation potentials are spontaneous discharges of whole motor units. This type of electrodiagnositic finding is found in each of the following disorders except:

 

1) Anterior motor horn disease

3) Cervical spondylytic myelopathy

2) Radiculopathy

5) Demyelinating myopathy

4) Muscle denervation

 

 

Fasciculation potentials are spontaneous discharges of the whole motor unit. This electrodiagnostic finding is found in: Anterior motor horn diseases

 

 

Cervical spondylytic myelopathy Radiculopathy

 

Demyelinating neuropathy

 

With denervation of skeletal muscle, electrodiagnostic testing includes: Fibrillation potentials

 

 

Low amplitude short bi- or triphasic deflections Positive sharp waves

 

 

Positive deflections followed by a negative wave Correct Answer: Muscle denervation

Which of the following statements is true concerning intraoperative acetabular fractures following uncemented total hip arthroplasty:

 

1) The incidence is lowest with an elliptical monoblock design.

3) The location of the fracture is most commonly anterosuperior.

2) The incidence is highest with a hemispherical modular cup design.

5) The location of the fracture is most commonly direct medial.

4) The location of the fracture is most commonly posterior superior.

 

Intraoperative acetabular fractures with uncemented cups are rare. This Mayo Clinic study showed a fracture rate of 3.5% with an elliptical monoblock cup. The rate with the monoblock cup was significantly higher than the elliptical modular and hemispherical modular designs (both <0.5%). The fractures were usually found posterior superior (12/21), direct posterior (posterior wall) (6/21), and much less commonly anterosuperior or medial. If the cup was unstable after the fracture, then it was removed, and another cup with screw fixation was used. All fractures healed uneventfully with no adverse sequelae. The authors recommend under-reaming ≤2 mm regardless of cup design.Correct Answer: The location of the fracture is most commonly posterior superior.

 

 

 

890. (3269) Q2-4112:

Which of the following statements is true concerning patients who have an immediate motor nerve palsy following a total hip arthroplasty:

 

1) Sciatic nerve palsy is more common than peroneal nerve palsy.

3) The majority of patients with an incomplete palsy will have a full recovery.

2) The majority of patients with a complete motor palsy will have a full recovery.

5) Previous hip surgery is not a signicant risk factor.

4) A body mass index of 30 or higher is a significant risk factor.

 

Farrell and colleagues from the Mayo Clinic recently reported a 0.17% rate of motor nerve palsy following 27,000 primary hip arthroplasties.

The important points to remember are:

 

Nerve distribution: peroneal 64%; sciatic 30%; femoral 6%

 

 

Complete nerve palsy 62%; incomplete 38% 87% of patients had a sensory deficit

 

 

Presumptive etiology in 26/47 (hematoma, traction, limb lengthening, laceration) Recovery

 

Complete palsy: full 36%; partial 39%; none 25%

 

Incomplete palsy: full 39%; partial 17%; none 44%

 

 

Leg lengthening is a significant risk factor (conditional logistic regression) Odds ratio 1:1

 

 

Average lengthening 1.7 cm (range: 1.1 cm to 4.4 cm) Significant factors (univariate logistic regression)

 

 

 

 

Developmental dysplasia Post-traumatic arthritis Posterior approach Uncemented arthroplasty

 

46% required a walking aid at follow-up

Correct Answer: Previous hip surgery is not a signicant risk factor.