bone, joint, soft tissue 2 Flashcards

1
Q

what cartilage tumor is more common in younger people

A

enchondroma

benign

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2
Q

what cartilage tumor is more common in older people

A

chondrosarcoma

malignant

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3
Q

osteochondroma

A

aka exostosis
benign cartilage-capped tumor that is attacehd to underlying skeleton by bony stalk
most common benign bone tumor
85% solitary

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4
Q

osteochondroma morphology

A

sessile or pedunculated
1-20cm
cap is benign hyaline cartilagecovered in perichondrium

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5
Q

osteochondroma x-ray

A

can see mm pull lines

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6
Q

osteochondroma clinical

A

usually stop growing at time of growth plate closure

symptomatic tumors are cured by simple excision

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7
Q

multiple hereditary exostosis

A

5-20% progress to chondosarcoma

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8
Q

chondromas

A

benign tumors of hyaline cartilage that usually occur in bones of enchondral origin

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9
Q

chondromas that arise in medullary cavity

A

enchondromas

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10
Q

chondromas that arise on surface of bone

A

juxtacortical chondromas

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11
Q

enchondromas

A

most common intraosseous cartilage tumros
20-50
appear as soliatry metaphyseal lesions of tubular bones of hand and feet

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12
Q

chondromas xray

A

circumscribed lucencies with central irregular calcifications, sclerotic rim and intact Cx
<3cm

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13
Q

what NONHEREDITARY disorders can cause multiple enchondromas

A

ollier disease
maffucci syndrome
can both be more cellular with cytologic atypia

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14
Q

chondromas clinical

A

growth potential limited
Tx-usually observation or curettage
solitary rarely undergo sarcomatous transformation

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15
Q

maffucci syndrome

A

also have spindle cell hemangiomas

at risk for ovarian carcinomas and brain gliomas

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16
Q

chondrosarcoma

A

malignant tumors that produce cartilage
2nd most common malignant tumor of bone
usually 40+

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17
Q

where do chondrosarcomas commonly arise

A

axial skeleton, pelvis, shoulder, ribs

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18
Q

chondrosarcomas xray

A

calcified matrix appears as foci of flocculent densities

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19
Q

chondrosarcomas clinical

A

painful, progressively enlarging masses
direct correlation btwn grade and behavior of tumor
most present as grade I which rarely metastasize
grade 3- 70% mets to lungs

20
Q

Tx of chondrosarcomas

A

surgical excision

chemo

21
Q

Ewing sarcomas

A

malignant bone tumor with primitive round cells w/o obvious differentiation
now grouped with PNET tumors

22
Q

Ewing sarcomas presentation

A

80% <20
usually arise in diaphysis of long bones and flat bones of pelvis
painful enlarging masses with warmth and swelling and leukocytosis mimicking infection

23
Q

ewings xray

A

destructive lytic tumor with permeative margins that extends into surrounding soft tissue
onion skinning
homer-wright rosettes

24
Q

Tx of Ewings

A

neoadjuvant chemo with surgery and +/- radiation

long term cure 50%

25
giant cell tumor
``` dominated by multinucleated osteoclast-type giant cells aka osteoclastoma uncommon benign, but locally aggressive 20-40 ```
26
giant cell xray
soap bubble
27
Tx of giant cell
curettage 40-60% locally recur RANKL inhibitor denosumab
28
giant cell mets
4% mets to lungs, but can spontaneously regress and seldom fatal
29
aneurysmal bone cyst (ABC)
multiloculated blood-filled cystic spaces usually first 2 decades metaphysis of long bones and post vertebral bodies pain and swelling
30
ABC xray
eccentric expansible lesion with well defined margins most are completely lytic and often contain thin shell of reactive bone at periphery fluid-fluid levels
31
ABC clinical
surgery | low recurrence rate
32
lesions stimulating primary neoplasms
fibrous cortical defect- small (.5cm) | nonossifying fibromas- (5-6cm)
33
fibrous cortical defects
aka metaphyseal fibrous defects extremely common 30-50% of kids 2+ cast majority arise in distal femur and proximal tibia, almost half are b/l or multiple
34
fibrous cortical defect histo
pinwheel
35
clinical fibrous cortical defect
asymptomatic detected incidentally Bx rarely needed spontaneous resolution
36
clinical nonossifying fibromas-
pathologic fracture and may require Bx and surgery
37
fibrous dysplasia
benign tumor likened to localized developmental arrest | all normal components are present, just do not differentiate into mature structures
38
fibrous dysplasia clinical patterens
monostotic- single bone polystotic- multiple bones mazabraud syndrome McCune-Albright syndrome
39
mazabraud syndrome
fibrous dysplaisa (usually poly) and soft tissue myxomas
40
McCune-Albright syndrome
polyostotic disease, cafe-au-lait spots, endocrine abnormalities, (precocious puberty)
41
fibrous dysplasia xray
ground glass appearance | well defined margins
42
monostotic fibrous dysplasia clincal
B=G usually early adolescence often stops enlarging when growth plate closes femur, tibia, ribs, jaw, calvarium, and humerus usually asymptomatic, but may cause pain, fracture, or leg length discrepancies Tx- only if symptomatic curettage
43
polystotic fibrous dysplasia clincal
manifests earlier then mono may continue to be symptomatic into adulthood femur, skull, tibia, humerus, ribs, fibula, radius, ulan, mandible, vertebrae may require multiple sugeries bisphosphonates can Tx pain rarely transforms into sarcoma
44
75% of bone mets are from what
``` prostate breast kidney lungs metastatic bone CA much more common then primary bone CA ```
45
prostate mets
usually blastic
46
kidney, GI, and melanoma mets
lytic
47
what translocation is assocaited with Ewing sarcoma
t(11,22)