• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/43

Click to flip

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