Lecture 8- Musculoskeletal pathology Flashcards

(33 cards)

1
Q

… aka “brittle bone disease, these are a group of hereditary bone disorders with abnormal synthesis of type 1 collagen

A

osteogenesis Imperfecta (OI)

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2
Q

… and … may be seen as components of OI

A

blue sclera

opalescent teeth (dentinogenesis imperfecta-like)

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3
Q

most OI’s are autosomal…

A

dominant

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4
Q

…. aka “marble bone disease” is a group of rare hereditary bone disorders with defective bone remodeling (osteoclast dysfxn)

A

osteopertosis

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5
Q

affected bone of osteopetrosis is … but structurally … and…

A

dense

unsound

weak

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6
Q

patients with osteopetrosis are prone to .. and …

A

fractures

infections (osteomyelitis)

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7
Q

in osteopetrosis, compression of … can lead to …

A

cranial foramina

blindness, deafness

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8
Q

in osteopetrosis, bone can replace … and lead to …

A

marrow stem cells

pancytopenia (anemia, thrombocytopenia, leukopenia)

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9
Q

… is an increased porosity of the skeleton resulting from reduced bone mass and leading to bone fragility

A

osteoporosis

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10
Q

most common form of acquired, metabolic bone disease?

A

osteoporosis

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11
Q

… million people in the US have osteoporosis and … million have osteopenia

A

10

44

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12
Q

postmenopausal women are at the greatest risk for osteoporosis because it is associated with…

A

reduced estrogen

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13
Q

most common sites of osteoporosis?

A

vertebral bodies, pelvis, femoral neck and other weight bearing bones

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14
Q

osteoporosis may lead to … and subsequent…

A

kyphoscoliosis

reduced respiratory fxn

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15
Q

dx for osteoporosis

A

dual X-ray absorptiometry (DEXA scan)

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16
Q

tx for osteoporosis

A

diet/exercise

calcium with vit D supp

bisphosphonates

hormone replace. therapy

monoclonal Ab (denosumab, Prolia)

17
Q

prognosis for osteoporosis

18
Q

…. disease is an abnormal dense bone formation which is structurally weak and prone to fracture. usuall affects multiple bones (85% polyostitic) and affects adults over the age of 40

A

paget disease

19
Q

etiology of paget disease?

A

unknown but paramyxovirus infection suspected

20
Q

T/F most cases of paget disease are asymptomatic

A

true, may be detected on routine radiographs or blood studies

21
Q

what symptoms could you see in paget disease

A

bone enlargement

bowing of leg bones

cranial nerve compression

pain

fractures

22
Q

a very distinct feature that you could see from paget disease is …. which is termed a “lion face” characterized by overgrowth of facial and cranial bones and a slight increased risk (1% lifetime) for development of sarcomas (particularly osteosarcoma)

A

leontiasis ossea

23
Q

paget disease happens in these 3 phases:

A
  1. osteoclactis activity , hypervascularity, bone loss
  2. osteoclastic and osteoblastic proliferation
  3. late osteosclerotic phase
24
Q

what is the bone called in paget disease due to its histologic appearance

25
tx for paget disease
calcitonin, bisphosphonates analgesic for bone pain
26
... is the inappropriate secretion of PTH
hyperparathyroidism
27
Primary hyperparathyroidism is due to ... , ... or ... and is more ... but less...
parathyroid hyperplasia, adenoma, carcinoma more severe less common
28
Secondary hyperparathyroidism leads to poor ... and altered .... commom complication of ESRD or vit. D deficiency
calcium retention vit. D metabolism
29
PTH actions
osteoclastic activation increased calcium absorption by the kidneys increased vit. D syn (kidneys) promoting calcium absorption from gut ALL increase serum calcium
30
... is infection of bone and marrow and are usually bacterial
osteomyelitis
31
bacteria can colonize in bone one of 3 ways:
hematogenous spread (staph) contiguous infection (odontogenic) implantation following fracture of surgery
32
T/F osteomyelitis is usually asymptomatic
false. associated with pain/tenderness, possible overlying erythema or swelling
33
tx for osetomyelitis
drainage antibiotics surgical debridement