MSK path VII Flashcards

(47 cards)

1
Q

what are the most likely cartilage forming tumors ages 10-30

A

chondroblastoma and chondromyxoid fibroma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what cartilage forming tumor is more common in older patients >25 y.o

A

clear cell chondrosarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is osteochondroma

A

exostosis

benign cartilage capped tumor attached to skeleton by stalk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

msot common benign bone tumor

A

osteochondroma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what makes cap of osteochondroma

A

hyaline cartilage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

are osteochondromas lytic lesions

A

no

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

clinical course osteochondroma

A

stop growing at time of growth plate closure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Symptomatic tumor Tx osteochondroma

A

excision

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

when can osteochondromas progress to chondrosarcomas

A

in those with multiple hereditary exostosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

chondromas

A

benign tumors of hyaline cartialge

enchondral region of bone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is name of chondroma arising in medullary cavity

A

enchondroma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are chondromas called that arise on surface of bone

A

juxtacortical chondromas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

most common intraosseous cartilage tumor

A

enchondromas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

presentation enchondroma

A

solitary metaphyseal lesion of tubular bones of hands and feet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

radiograph of chondroma

A

circumscribe lucencies with central irregular calcifications

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

nonhereditary disorders with multiple enchondromas

A

ollier disease and Maffucci syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

how is Maffucci syndrome distinguished

A

spindle cell hemangioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

morphology enchondroma

A

< 3cm
gray blue and translucent
well circumscribe nodules of hyalin with benign chondrocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

get ollier disease and maffucci syndrome enchondromas mixed with what

A

chondrosarcomas

20
Q

casing of enchondroma

A

thin layer reactive bone

21
Q

Maffucci syndrome patients at risk of developing what

A

ovarian carcinomas and brain gliomas

22
Q

chondrosarcoma

A

maligant tumor that produces cartilage

23
Q

subclassifications chondrosarcomas

A

conventional (produce hyaline)
clear cell
de differentiated
mesenchymal

24
Q

age of chondrosarcoma

25
where do chondrosarcomas arise
axial skeleton, pelvis, shoulder, ribs
26
XR chondrosarcoma
calcified matrix with foci of flocculent densities
27
presentation chondrosarcoma
painful! progressively enlarging mass nodular pattern of cartilage produce scalloping
28
matrix in chondrosarcomas
gelatinous or myxoid, can ooze
29
grade 3 chondrosarcoma
high cellularity extreme pleomorphism with bizarre tumor giant cells and mitoses
30
scalloping of bone on XR and increased Ca 65 y.o
chondrosarcoma
31
prognosis grade 1 chondrosarcoma
5 yr 80-90%
32
where do chondrosarcomas mets to
lungs
33
Tx conventional chondrosarcoma
wide surgical excision
34
Tx mesenchymal and dedifferentiated tumors
excised and Tx with chemo because aggressive
35
Ewing Sarcoma
malignant bone tumor characterized by primitive round cells without obvious differentiation
36
What are in ewing sarcoma family tumors
ewing sarcoma | and primitive neuroectodermal tumor PNET
37
bone tumors with youngest age presentation <20 y.o
ewing sarcoma family tumors
38
where do ewing tumors arise
diaphysis of long tubular bones in medullary cavity
39
clinical presentation ewing sarcomas
pain, tender warm and swollen | sometimes like infection: fever, inc sed rate, anemia, leukocytosis
40
radiograph ewings
destructive lytic lesion with permeative margins that extend into soft tissues
41
onion skin fashion of periosteal reaction
ewing sarcoma
42
translocation in ewing sarcoma
11;22
43
gross morphology ewing sarcoma
soft tan white and hemorrhage and necrosis sheets of uniform small cells that are larger thatn lymohocytes little cytoplasm
44
homer wright rosettes (round groupings with central fibrillary core)
neuroectoderm differentiation---- ewings sarcoma
45
rossetting and PAS +
ewings sarcoma
46
Tx ewing like tumors and ewings
neoadjuvant chemo with surgical excision | +/- irradiation
47
prognostic finding for ewings
amount of chemo-induced necrosis