Bone Pathology - Sheet1 Flashcards

1
Q

non-neoplastic bone disease

A

fractures involving healthy bone, osteoporosis (esp post menopausal) AND associated fractures, osteomalacia, osteomyelitis, avascular bone necrosis/infarction.

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2
Q

osteopenia differential

A

(decrease in bone mineralization) associated with osteoporosis (common), osteomalacia, malignancy, rare hereditary disorder.

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3
Q

osteomalacia definition

A

Definition: decreased bone mineralization with excess osteoid (wide osteoid seams)

Radiologically appears osteopenic (like osteoporosis) May present with diffuse skeletal pain (without fracture)

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4
Q

metastatic tumors to skeleton

A

neoplasm that is secondary metastatic site (from non-bone primary sites)

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5
Q

What is a pathological fracture?

A

fracture thorugh diseased bone

usually refers to fracture through tumorous or tumor-like bone

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6
Q

periosteum–Its response to trauma…

A

Periosteum functions to **repair bone **

full of nerves (so this hurts when you get kicked!)

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7
Q

puberty does what to the cartilagenous epiphyseal plate?

A

promotes vacularization… which promotes cartilage calcification.

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8
Q

What are the two critical regulatory molecules/enzymes for calcium homeostasis?

A

PTH and Vitamine D(OH)2

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9
Q

What vitamin is required for normal mineralization of bone osteoid?

A

Vit D(OH)2

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10
Q

Name some possible complications of healing bone

A

mal-alignment, non-union, mal-union, osteomyelitis, growth disturbance via breaking of epiphyseal plate), arthritis,

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11
Q

osteoporosis

A

A type of osteopenia due to bone atrophy caused by an imbalance of the bone remodeling process.

No markers, no clinical manifestations.

Currently defined as bone mineral density ≥ 2.5 standard deviations.

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12
Q

What are common observations for osteoporosis

A

kyphosis,

vit D(OH) –> Vit D(OH)2 rxn impaired = Diminished PTH

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13
Q

Why should osteoporosis be a diagnosis of exclusion?

A

Remember the often more treatable / reversible causes of secondary osteoporosis such as osteopenia (differential?)

Decreased bone mineralization (osteopenia) does not automatically = osteoporosis

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14
Q

What are the two most common causes of osteopenia?

A

decreased bone density; osteoporosis and osteomalacia

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15
Q

Best prevention for osteoporosis?

A

maximize peak bone mass (teens/young adults)

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16
Q

Primary Hyperparathyroidism

A

Hypercalcemia due to primary hyperplasia or Neoplastic enlargement of parathyroid glands.

High PTH promotes osteoclastic bone resorption/peritrabecular fibrosis = osteitis fibrosa.

17
Q

Classic Primary Hyperparathyroidism

A

asymptomatic and detected on biochemical screening studies primary type — *increased Ca and decreased P*

18
Q

Osteomalacia in children is called?

A

Rickets

19
Q

Osteomalacia: Biochemical profile/Labs

A

increased serum alkaline phosphatase (>90%)

Low serum Ca or P (50%)

Decreased urinary Ca excretion (33%)

increased PTH (40%)

Decreased 1, 25 dihydroxyvitamin D3 (50%)

20
Q

Parathyroid hormone

A

At low levels –> exerts anabolic effects (building bone) on osteoblasts and osteoclasts (indirect).

Chronic high PTH levels (primary hyperparathyroidism) –> causes an increase in blood [Ca++].

21
Q

What is the best prevention for osteoporosis?

A

maximize peak bone mass (teens/young adults) encourage weight-bearing exercise and Ca supplementation

22
Q

Bone pain, fever, local swelling and erythema, and no trauma. What should you think of?

A

Osteomyelitis

Staphylococcus aureus (95%)

Treatment is aggressive I.V. antibiotics.

23
Q

Most common cause of fungal osteomyelitis in non-immunosuppressed patients

A

Blastomycosis and coccidioidomycosis

24
Q

Avascular bone necrosis/infarction

A

infarction due to ischemia

Clinically: subchondral infarcts, medullary infarcts, multiple infarcts.

Common causes: femoral neck fractures or chronic corticosteroid Rx, SLE.

Treatment: often requires joint replacement

25
Q

Paget’s Disease of Bone

A

(Osteitis Deformans): deforming bone disease of middle-aged to elderly adults.

Epidemiology: Anglo-Saxon heritage highly associated

Pathophysiology: accelerated bone resporption followed by haphazard new bone formation.

Labs: increased alkaline phosphatase.

Three phases: i. Lytic—osteoclasts with bone resorption/ vascularity

ii. Mixed—osteoclasts with osteoblasts, vascularity
iii. Sclerotic—most characteristic radiologically (osteoblastic phase)

26
Q

Osteogenesis imperfecta

A

congenital disorder of type 1 collagen

27
Q

Tumor/tumor-like lesions involving bones

A

(bone pain, swelling, local redness, pathologic fracture)

Most common sources = most common visceral cancers: **lung, breast, prostate cancer **

Leukemia: always affects bone marrow

28
Q

Primary bone tumors/tumor-like lesions

A

most types arise in metaphyses of long bones

Malignant vs. Benign

29
Q

most common primary malignant tumor of children/young adults

A

Osteosarcoma

30
Q

Most common primary malignant tumor of middle-aged/older adults. May grow very large.

A

Chondrosarcoma

31
Q

Patients with sickle-cell anemia tend to get _________ osteomyelitis

A

salmonella