musculoskeletal path Flashcards

1
Q

group of hereditary conditions characterized by abnormal development of type I collagen, a major component of bone matrix, but also present in many tissues including skin, joints, and eyes

A

osteogenesis imperfecta (OI) aka brittle bone disease

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2
Q

group of rare hereditary disorders characterized by deficient osteoclastic activity with resultant defective bone remodeling

A

osteopetrosis aka marble bone disease

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3
Q

increased porosity of the skeleton resulting from reduced bone mass, with an associated increased bone fragility and increased prevalence of fractures

A

osteoporosis

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4
Q

fairly common bone disorder characterized by repetitive episodes of frenzied, regional osteoclastic activity and bone resorption (osteolytic stage), followed by exuberant osteoblastic activity and bone formation (mixed osteoclastic-osteoblastic stage), and finally by an apparent exhaustion of cellular activity (osteosclerotic stage)

A

Paget disease (osteitis deformans)

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5
Q

one of the most common endocrine disorders; an important cause of hypercalcemia

A

primary hyperparathyroidism

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6
Q

caused by any condition associated with a chronic depression in the serum calcium levels, because low serum calcium leads to compensatory over activity of the parathyroid glands

A

secondary hyperparathyroidism

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7
Q

____ is by far the most common cause of secondary hyperparathyroidism

A

renal failure

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8
Q

an infection spreading through the medullary spaces of a bone

A

osteomyelitis

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9
Q

characterized by progressive replacement of normal bone by fibrous tissue intermixed with unorganized, woven bone

A

fibrous dysplasia

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10
Q

bone and osteoid producing malignancy

A

osteosarcoma

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11
Q

most common disorder of the joints and is a very frequent, if not inevitable, part of aging

A

osteoarthritis (degenerative joint disease)

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12
Q

disorder caused by tissue accumulation of excessive amount of uric acid

A

gout

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13
Q

arises upon precipitation of urate crystals in the synovial fluid and membranes

A

acute gouty arthritis

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14
Q

group of inherited abnormalities of muscle which vary from mild motor weaknesses to severe life-threatening alterations (progressive degeneration of muscle fibers)

A

muscular dystrophies

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15
Q

X-linked recessive disorder caused by the absence of a structural protein, termed dystrophin, and is seen in about 1/3500 live male births

A

Duchenne muscular dystrophy

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16
Q

autoimmune disease which results in destruction of acetylcholine receptors in the neuromuscular junction and is manifested by weakness and prominent fatigability of voluntary muscles

A

myasthenia gravis

17
Q

the histopathologic features of Paget disease form a _______; radiographically, the bone shows a mixture of radiolucent-radiopaque areas referred to as _____

A

mosaic pattern of bone

cotton-wool pattern

18
Q

complication of Paget disease characterized by overgrowth of facial and cranial bones

A

leontiasis ossea (lion face)

19
Q

patients with Paget disease will display elevated levels of _____ and _____

A

urinary hydroxyproline (from increased bone resorption) and serum alkaline phosphatase (from increased bone apposition)

20
Q

treatment for paget disease

A

calcitonin, biphosphonates and analgesics (for bone pain)

21
Q

can be observed in patients with hyperparathyroidism; lesions are histopathologically identical to central giant cell granuloma of the jaws

A

osteitis fibrosa cystica (cyst-like brown tumors of bone)

22
Q

in more than 95% of cases, primary hyperparathyroidism is caused by ______

A

parathyroid adenomas or hyperplasia (less commonly by parathyroid carcinoma, but more severe)

23
Q

constellation of symptoms classically associated with primary hyperparathyroidism

A

painful bones, renal stones, abdominal groans, and psychic moans

24
Q

treatment for primary hyperparathyroidism

A

removal of the affected gland/tumor

25
Q

treatment for secondary hyperparathyroidism

A

renal transplant; vitamin D supplementation

26
Q

in osteomyelitis, bacteria can colonize the spaces within bone through one of three pathways:

A
  1. hematogenous spread (especially staph aureus)
  2. contiguous infection (i.e. odontogenic infections)
  3. direct traumatic introduction/implantation following fracture or surgery
27
Q

70% of all cases of fibrous dysplasia

A

monostotic fibrous dysplasia (single bone)

28
Q

pattern of cellular fibrous CT intermixed with elongated trabeculae of immature woven bone seen in fibrous dysplasia

A

Chinese characters

29
Q

the ill-defined radiopacity (seen in films with high detail) or ill-defined radiolucency in less detailed films- seen in fibrous dysplasia is described as _____

A

ground glass appearance

30
Q

_____ is the most frequent clinical presentation of osteosarcoma, however, _____ can also be the first sign of disease

A

a painful enlarging mass; pathologic fracture

31
Q

the radiographic appearance of osteosarcoma is generally that of a large, destructive mixed radiolucent-radiopaque lesion that may present with a ______

A

“sunburst” appearance

32
Q

a characteristics feature of osteosarcoma is the formation of an ____ between the neoplastic bone and the cortex, called _____

A

acute angle; Codman’s triangle

33
Q

the fundamental feature of osteoarthritis is _____; changes that follow in the underlying bone are secondary

A

degeneration of the articular cartilage