Chapter 146 - Malignant Soft Tissue Lesions Flashcards
pre-op radiation
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
chemotherapy for soft tissue sarcoma
only indicated in soft-tissue predominant ewings and rhabdomyosarcoma
what is the most important factor in determining overall prognosis/outcome in soft tissue sarcoma?
tumor stage
lymph node mets in what??
SCARE
synovial sarcoma
clear cell sarcoma
angiosarcoma
rhabdomyosarcoma
epitheloid sarcoma
undifferentiated pleomorphic soft tissue sarcoma
age 55-80
male 2:1
deep slow growing painless mass
low on T1
bright on T1
tx = surgery + radiation
Liposarcoma
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
histo of myxoid liposarcoma
histo of dedifferentiated liposarcoma
histo of pleomorphic liposarcoma
fibrosarcoma
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
dermatofibrosarcoma protuberans
t(17;22)
dermal skin layers
wide margins, imatinib (tyrosine kinase inhibitors)
synovial sarcoma
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
epitheloid sarcoma
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
clear cell sarcoma
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
rhabdomyosarcoma
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