Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
43 Cards in this Set
- Front
- Back
liposarcoma
|
le of adults, rare in children
|
|
embryonal rhabdomyosarcoma
|
head/neck of children, rare in adults
|
|
sarcoma
|
metastasize via bloodstream
|
|
nodular fasciitis
|
adults, volar forearm, chest, back
reactive pseudosarcomatous, solitary, rapid growth, sometimes painful w/in weeks, 10-15% previous trauma, plump (myo)fibroblasts randomly arranged, short fasicles (looks like tissue culture), myxoid bg (blue), extravasated rbc, lymphocytes, mitotic figures, scar-like collagenization over time (less cellular) |
|
grading criteria
|
histological type, cellularity, pleomorphism, mitotic rate, extent of necrosis (<15% grade 2, 15%+ grade 3)
probability of metastasis, overall survival does not predict recurrence higher grade responds better to chemo |
|
myositis ossificans
|
athletic adolescents, ya, 50% previous trauma, reactive pseudosarcomatous
early: swollen, painful, similar to nodular fasciitis wks: less painful, firm, zonation late: painless, hard, well circumscribed, complete bone metaplasia |
|
gardner syndrome
|
fap, osteomas, dental anomalies, epidermal inclusion cysts, colorectal carcinoma, ***desmoid tumor
|
|
turcot syndrome
|
fap, medulloblastoma
|
|
df
|
dermatofibroma, benign, dermis/subcutis, slow growing, painless, mobile, small <1cm, well circumscribed, bland spindle cells w/ delicate cyt, ***storiform pattern (more pinwheel than whorl), collagen prod, no mitosis/necrosis/atypia
|
|
dfsp
|
ya, dermis/subcutis of trunk/extremities
dermatofibrosarcoma protuberans, modular polypoid lesion, malignant, low grade (<5% mets), slowly growing, 30% recur, ***storiform pattern, ***honeycomb infiltration (leaves some alone) into adipose |
|
fibrosarcoma
|
adults 40-60 yo, deep soft tissue of upper/lower extremities, trunk, head/neck
subcutis if assoc w/ dfsp, scars, burns, rad therapy dx of exclusion, solid growth of hyperchromatic malignant spindle cells, hypercellular, ***herringbone pattern |
|
mfh
|
malignant fibrohistiocytoma, most common of adults, mm of prox extremities, retroperitoneum, cutaneous (atypical fibroxanthoma afx, rarely disseminates)
unknown origin, pleomorphic variant of otehr sarcoma?, aggressive, 30-50% recur (not cutaneous), angiomatoid subtype is indolent |
|
lipoma
|
most common 1ary soft tissue tumor of adult, looks like nl tissue (adipocytes, thin strings of ct/capillaries), well encapsulated, lobulated, soft, solitary, freely movable, painless, benign
|
|
spindle cell lipoma
|
sc tissue of scapula (neck, upper back, shoulder) in middle age/elderly males, bipolar spindle cells, can be very cellular, some atypia (floret cells - multinuc giant cell)
|
|
fibroma molle
|
skin tag, very soft, pedunculated, mix of mature fibrous tissue and fat on surface
|
|
angiolipoma
|
***painful sc in forearm of ya, vascular channels w/ microthrombi
|
|
intramuscular lipoma
|
lipomatous growth w/in skeletal m fibers, doesn't destroy, ddx liposarcoma w/ skeletal m
|
|
lipoblastoma
|
children <3 yo, upper/lower limb, m2x>f, local sc
immature fat cells w/ less cyt, granular, clearer nuc, tend to mature into fat |
|
lipoblastomatosis
|
diffuse lipoblastoma --> skeletal m
|
|
hibernoma
|
very rare, from brown fat (neck, axilla, mediastinum, perirenal), encapsulated, sc
|
|
well-differentiated liposarcoma
|
50-70 yo, 75% extremities
sclerosing-spindle cell more common than lipoma-like but w/ atypical cells, 5-15% dediff (look like fibrosarcoma/mfh, retroperitoneum, extremities, recurrances --> mets to lung), giant marker, ***ring chr, local recurrence high, no mets |
|
myxoid liposarcoma
|
25-45 yo, 75% extremities
low grade: lipoblasts, chicken-wire/net vessels, myxoid bg high grade: same as low but w/ solid areas of round cells w/o cyt, chr t(12;16), recurrence, metastasis, 40% of liposarcoma |
|
pleomorphic liposarcoma
|
deep soft tissue of limb/limb girdle
looks like pleomorphic mfh, high grade w/ high metastatic potential, very aggressive, very poor prognosis, 20% of liposarcoma, abundant giant cells |
|
round cell liposarcoma
|
round-oval cells, multivacuole cyt, central hyperchromatic nuc, signet ring lipoblasts
|
|
lipomatosis
|
multiple lipomas
|
|
rhabdomyoma
|
heart, children, benign
|
|
rhabdomyosarcoma
|
malignant, most common soft tissue sarcoma <20 yo, head/nec, gu, extremities
aggressive, tx surg/chemo/rads, 65% children cured, adults less successful, immounohisto (desmin, myoglobin, myogenin pos) |
|
embryonal rms
|
60% of rms, <10 yo, nasal cavitis, orbit, mid ear, prostate, paratesticular
botrioid better prognosis, clusters of grapes, pedunculated nodules, hypercelular, rhabdoid cells w/ eosinophilic cyt, eccentric/round nuc but not signet ring, can see tadpole cells w/ striations, **hollow organs like vag, nasopharynx, biliary tract, bladder of babies |
|
alveolar rms
|
10-25 yo, deep mm of extremities
worse prognosis, small cells w/ high n/c ratio, psuedoalveolar pattern, chr t(2;13), t (1;13) |
|
pleomorphic rms
|
thigh, adults, grows rapidly
|
|
leiomyoma
|
skin/sc: erectores pilorum, erector m of nipple, tunica media of bv
deep soft tissue: retroperitoneum, omentum, mesentary, broad ligament can also be iv benign, fascicles of spindle cells 90 deg, ***cigar shaped nuc, fibrillary cyt, no mitosis/atypia/necrosis, immunohisto (desmin, actin, vimentin pos), can be vascular (painful if skin/sc), epithelioid |
|
leiomyosarcoma
|
malignant, extremities, retroperitoneum, cutaneous, female genital, deep soft tissue, f>m
10-20% all sarcoma, death by local extension or mets (lung), short fascicles, 90 deg interweaving, ***atypical cigar-shaped nuc, atypical mitosis, fibrillar cyt (trichrome), immunohisto (desmin, actin, vimentin pos), cyt/nuc vacuolated |
|
synovial sarcoma
|
20-40 yo, lower extremities, deep seated (parapharyngeal, abd wall)
unclear cell of origin, recapitulate synovium, 10% of all sarcoma, only 10% intraarticular, mets to lung, ***chr t(x;18) syt-ssx gene fusion biphasic: spindle, epithelial (glands) monophasic: spindle (like fibrosarcoma), epithelial (glands, rare) |
|
benign synovioma
|
gct of tendon sheath
|
|
most common soft tissue tumor
|
lipoma
|
|
liposarcoma in retroperitoneum fatal how?
|
local aggressiveness to bv, ureter, other vital organs
|
|
most common soft tissue tumor in children
|
rhabdomyosarcoma
|
|
most common malignant soft tissue tumor in general
|
metastatic cancer
|
|
hemangioma
|
benign, bv, head/neck, many hamartomas, capillary and cavernous subtypes
|
|
angiosarcoma
|
head/neck skin of elderly
malignant, anastomosing vascular channels w/ malignant endothelial cells |
|
stewart-treves syndrome
|
lymphangiosarcoma, extremities w/ longstanding lymphedema (postmastectomy)
|
|
kaposi's sarcoma
|
middle age/older intially cutaneous nodules of distal leg
bland plum spindle cells w/ slit-like vascular spaces w/ rbc/hemosiderin |
|
extraskeletal ewing's sarcoma
|
lower extremity, paravertebral
|