Radiology 3 Flashcards

1
Q

tumors most likely in children

A

benign: ABC, SBC, osteoid osteoma
malignant: osteosarcoma, Ewing sarcoma, lymphoma

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2
Q

tumors most likely in young adults

A

benign: giant cell, osteochrondroma
malignant: lymphoma, osteosarcoma

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3
Q

tumors most likely in older adults

A

benign: non usually newly found in this group
malignant: metastasis, myeloma, chondrosarcoma, lymphoma

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4
Q

tumors in epiphyseal or bone end

A

giant cell tumor

chondroblastoma

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5
Q

tumors in diaphyseal bones

A

ewing sarcoma
lymphoma
advancing/enlarging metaphyseal lesions

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6
Q

what do tumors look like in bone?

A

dense, white, “hard” appearance

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7
Q

what do tumors look like in cartilage?

A

stippled, punctate, speckled, dotted calcifications

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8
Q

what do tumors look like that are fibrous?

A

hazy, smokey, cloudy, ground glass

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9
Q

what do tumors look like that are lytic/lucent?

A

pure “empty” hole in the bone, punched out, moth-eaten

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10
Q

which 3 primary cancers are most likely to lead to metastasis?

A

lung
breast
prostate

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11
Q

where in the body will metastasis usually been seen?

A

highly vascular tissue (pedicles, metaphyses)

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12
Q

what’s the difference between lytic metastasis and blastic metastasis?

A

lytic- holes in bone

blastic- random increased densities

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13
Q

metastasis key possible findings

A

absent pedicle
polyostotic locations, multiple sized lesions, less well-defined margins
lytic, blastic, or mixed densities
usually no periosteal reaction or soft tissue mass
ivory vertebra
pathological collapse of vertebrae, could be vertebra plana

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14
Q

metastasis management (labs)

A

blood: hypercalcemia, elevated alkaline phosphatase, ESR, CRP

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15
Q

metastasis (imaging)

A

CT best for defining degree of bony destruction at each site
MRI best for evaluating marrow destruction
radionuclide scintigraphy- best for searching for multiple sites of involvement
chest films for evaluating common metastatic site

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16
Q

metastasis referral

A

oncologist
primary allopath
orthopedist

17
Q

primary malignant tumors (from most common to least common)

A
multiple myeloma
osteosarcoma
chondrosarcoma
ewing sarcoma
lymphoma
18
Q

multiple myeloma key possible findings

A

punched out lesions
raindrop skull
usually no soft tissue mass or periosteal reaction
pathological collapse of vertebrae, could be vertebra plana

19
Q

multiple myeloma management (labs)

A

blood: M spike on protein electrophoresis, hyperglobinemia with reversed A/G ratio, normocytic normochromic anemia, thrombocytopenia, elevated creatine and BUN levels
urine: bence jones proteins, hypercalciuria

20
Q

multiple myeloma management (imagins)

A

CT best for defining degree of bony destruction at each site
MRI best for evaluating marrow destruction
bone scan best for searching for multiple sites of involvement, but could be cold
chest films for evaluating common metastatic site

21
Q

multiple myeloma referral

A

oncologist
primary allopath
orthopedic

22
Q

osteosarcoma key possible findings

A

second most common primary malignant tumor overall, but most common for children
ages 10-25 and >60 due to malignant degeneration of “osteo” tumors
location: usually metaphysis, usually knee or humerus
aggressive and metastatic
periosteal reactions (spiculated, sunburst, laminated, codman’s triangle possible)

23
Q

chondrosarcoma key possible findings

A
3rd most common primary malignancy
50-70 years
mostly located in pelvis, metaphysis
aggressive and metastatic
stippled, punctate, speckled, dotted
24
Q

ewing sarcoma key possible findings

A

4th most common primary malignancy overall, 2nd most common in children (10-25)
aggressive and malignant
located in leg bones, pelvis, anywhere
lytic, moth-eaten appearance, with laminated periosteum

25
Q

key location for ewing sarcoma

A

diaphysis

26
Q

lymphoma of bone key possible findings

A

5th most common primary malignancy
any age for non-hodgkin’s, 20-40 for hodgkin’s (reed-sternberg cells)
spine: ivory vertebra, compression fractures
extremities: lytic diaphysis location (mimics Ewing)