Chapter 146 - Malignant Soft Tissue Lesions Flashcards

1
Q

pre-op radiation

A

lower dose
twice the wound complications
forms a fibrotic shell around the tumor
decreases surrounding tumor edema

*surgery should be delayed 3-4 weeks following completion of radiation

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2
Q

chemotherapy for soft tissue sarcoma

A

only indicated in soft-tissue predominant ewings and rhabdomyosarcoma

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3
Q

what is the most important factor in determining overall prognosis/outcome in soft tissue sarcoma?

A

tumor stage

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4
Q

lymph node mets in what??

A

SCARE

synovial sarcoma
clear cell sarcoma
angiosarcoma
rhabdomyosarcoma
epitheloid sarcoma

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5
Q

undifferentiated pleomorphic soft tissue sarcoma

A

age 55-80
male 2:1

deep slow growing painless mass

low on T1
bright on T1

tx = surgery + radiation

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6
Q

Liposarcoma

A

age 50-80
males>females

well differentiated variant = ALT in the extremitites, ring chromosome 12, MDM2 expression

myxoid liposarcoma t(12;16)
can met to spine, and abdomen
Need CT C/A/P and MRI/CT spine for staging

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7
Q

histo of myxoid liposarcoma

A
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8
Q

histo of dedifferentiated liposarcoma

A
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9
Q

histo of pleomorphic liposarcoma

A
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10
Q

fibrosarcoma

A

males>females 30-55
slow growing painless mass around the knee/thigh
can get ulceration of the skin in superficial lesions

histo: fasiculated herringbone pattern with bland fibroblasts

tx: wide resection and radiation

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11
Q

dermatofibrosarcoma protuberans

A

t(17;22)

dermal skin layers

wide margins, imatinib (tyrosine kinase inhibitors)

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12
Q

synovial sarcoma

A

juxta-articular - these are NOT intra-articular lesions

young people -15-40
male>females

t(X;18) - SYT-SSX

calcifications on plain XR
Low T1, high T2 (like all soft tissue sarcomas)

path: biphasic - gland-like epithelia plus elongated spindle cells

lymph node mets in 10-12%
heavily calcified lesions = better prognosis

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13
Q

epitheloid sarcoma

A

age 10-35
males 2:1

expresses Ca-125

frequently involves the hands, forearm, fingers - most common soft tissue sarcoma of the hand/wrist

nodular pattern with central necrosis

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14
Q

clear cell sarcoma

A

20-40yo, females>males
malignant melanoma of soft parts

t(12;22)

foot, ankle, knee, hand

frequently mets to nodes
frequently mets to lungs with a terrible prognosis
no effective chemo

tx : wide excision and radiation

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15
Q

rhabdomyosarcoma

A

occurs in children 0-20

embryonal occurs age 0-4 males>females

alveolar more in adolescents <20 male=female
t(2;13) Pax-Fkr

head/neck, retroperitoneal, or GU

staging needs to include a bone marrow biopsy

path: stains for desmin, myoglobin, and MyoD1

treatment: multimodal chemo!!!! (besides soft tissue ewings this is the ONLY soft tissue sarcoma that is treated with chemo)
vincristine, cyclophosphamide
ifosfamide

regional node mets common

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