Lecture 8- Musculoskeletal pathology Flashcards

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

A

guarded

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

A

mosaic

25
Q

tx for paget disease

A

calcitonin, bisphosphonates

analgesic for bone pain

26
Q

… is the inappropriate secretion of PTH

A

hyperparathyroidism

27
Q

Primary hyperparathyroidism is due to … , … or … and is more … but less…

A

parathyroid hyperplasia, adenoma, carcinoma

more severe

less common

28
Q

Secondary hyperparathyroidism leads to poor … and altered ….

commom complication of ESRD or vit. D deficiency

A

calcium retention

vit. D metabolism

29
Q

PTH actions

A

osteoclastic activation

increased calcium absorption by the kidneys

increased vit. D syn (kidneys) promoting calcium absorption from gut

ALL increase serum calcium

30
Q

… is infection of bone and marrow and are usually bacterial

A

osteomyelitis

31
Q

bacteria can colonize in bone one of 3 ways:

A

hematogenous spread (staph)

contiguous infection (odontogenic)

implantation following fracture of surgery

32
Q

T/F osteomyelitis is usually asymptomatic

A

false. associated with pain/tenderness, possible overlying erythema or swelling

33
Q

tx for osetomyelitis

A

drainage
antibiotics
surgical debridement