Musculoskeletal Flashcards

1
Q

Multinucleated giant cells residing in Howship lacunae

A

Osteoclasts

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2
Q

Backbone of bone matrix is made up of

A

type I collagen

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3
Q

Woven bone

A

Collagen is deposited randomly (fetus, growth plates)

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4
Q

Lamellar bone

A

Collagen is deposited in an orderly fashion

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5
Q

Osteogenesis Imperfecta

A

deficiency in synthesis of type I collagen

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6
Q

blue sclera, small misshapen yellow teeth, deafness

A

Osteogenesis Imperfecta

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7
Q

Type I (Osteogenesis Imperfecta Tarda)

A

acquired mutation, mild

most common form, fractures in early childhood, XR shows old Fx

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8
Q

Type II (Osteogenesis Imperfecta Congenita)

A

rare inherited, Fx & bone malformations at birth

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9
Q

Death in osteoporosis pt is likely d/t

A

pneumonia and PE

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10
Q

Osteoporosis

A

imbalance between bone resportion and formation ↑porosity of bones

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11
Q

2 Types of Osteoporosis

A

age-related (low osteoblast Fx)

postmenopausal (high osteoclast Fx)

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12
Q

Osteoporosis S/S

A

fractures of the distal forearm, vertebrae or proximal femur, compression microfractures, lumbar lordosis, kyphoscoliosis

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13
Q

Osteoporosis Histology

A

excessive but proportional reduction in both mineral and matrix phases of bone

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14
Q

Osteopetrosis

A

osteoclast dysfunction and diffuse skeletal sclerosis

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15
Q

Osteopetrosis defect

A

defect in carbonic anhydrase II –> blocked matrix solubilization and resorption

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16
Q

Erlenmeyer flask deformity

A

Osteopetrosis

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17
Q

Malignant Osteopetrosis S/S

A

HSM d/t extramedullary hematopoiesis, mild cranial nerve deficits

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18
Q

Paget Disease (Osteitis Deformans)

A

hereditary disease of osteoclast dysfunction and matrix madness (high osteoclast Fx -> burn-out -> high osteoblast Fx)

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19
Q

Paget Disease (Osteitis Deformans) cause

A

fifth decade, may be d/t paramyxoviruses

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20
Q

Paget Disease (Osteitis Deformans) affects

A

long bones, pelvis, spine, skull, with bone becoming thick, soft, and porous

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21
Q

Paget Disease (Osteitis Deformans) Histology

A

mosaic pattern of lamellar bone

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22
Q

thick porous skull

A

Paget Disease

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23
Q

Paget Disease

A

Leonine facies (leontiasis ossea), skull invagination (platybasia), and femur bowing

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24
Q

Increased hat size

A

Paget Disease

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25
Paget Disease bone findings
light, soft, porous, ossified, sclerotic bone
26
Paget Disease
increased risk for osteosarcoma
27
Rickets & Osteomalacia
vitamin D deficiency or disturbance in Vit D metabolism
28
rosary bead formation at costochondral jxn
Rickets
29
Long standing hyperparathyroidism can lead to
osteitis fibrosa cystica
30
Osteonecrosis
ischemia → infarction of bone and marrow
31
Causes of Osteonecrosis
fracture, thrombosis, embolism, blood vessel injury, ↑intraosseous pressure
32
Medullary infarcts
infarcts of cancellous bone and marrow, but NOT cortex (SILENT)
33
Subchondral infarcts
involve bony plates and epiphysis, but spare the cartilage
34
Osteomyelitis
hematogenous spread, majority of cases are d/t S. aureus
35
Osteomyelitis IN A SICKLE CELL pt
Salmonella
36
Osteomyelitis Histology
Bone fragment becomes devitalized and necrotic (sequestrum) + sleeve of reactive bone at periphery (involucrum)
37
Tuberculous osteomyelitis often involves
thoracic/lumbar spine (Pott’s disease)
38
Tuberculous osteomyelitis
miliary TB
39
Osteoma
benign bone tumor, face, Gardner Syndrome
40
Osteoid Osteoma S/S
painful tumors, release PGE2, pain relieved by aspirin
41
Osteoid Osteoma Histo
radiolucent nidus surrounded by densely sclerotic bone
42
Osteoid Osteoma affects
femur & tibia
43
Osteoblastoma S/S
dull, achy pain that does NOT respond to salicylates
44
most common PRIMARY malignancy of bone
Osteosarcoma
45
most osteosarcomas arise in
long bones (near knee)
46
Osteosarcoma genetic link
associated with p53 and RB mutations
47
Osetochondroma
cartilage capped outgrowth near epiphyseal growth plate of long tubular bones
48
Chondroma
benign hamartomatous tumors composed of hyaline cartilage
49
Ollier disease
multiple endochondromas
50
Chondroma typically affect
females, occur in 3rd-4th decade of life, metaphyses
51
Fibrous Cortical Defect and Non-ossifying Fibroma
extremely common congenital defects in up to 50% of children older than age 2, b/l, multiple, most spontaneously regress
52
Fibrous Cortical Defect and Non-ossifying Fibroma Histo
fibroblasts in pinwheel pattern
53
Fibrosarcoma and Malignant Fibrous Histiocytoma Histo
malignant fibroblasts in “herringbone” pattern
54
Ewing Sarcoma
highly malignant small round cell tumor, neural origin
55
McCune Albright Syndrome
Fibrous Dysplasia
56
Giant Cell Tumor (Osteoclastomas)
"soap bubble" appearance, aggressive benign, epiphyseal
57
Myositis Ossificans
develop in athletic young adult in high contact sport following trauma; usually found in subcutis or muscle of proximal extremity
58
Dupuytren contracture
palmar fibromatosis
59
Peyronie disease
Penile fibromatosis
60
rhabdomyosarcoma
most common variant is embryonal rhabdomyosarcoma