TUMOR
ORIGIN · GENETICS
FEATURES
CLUE
Lipoma
most common soft tissue tumor
Benign mature adipocytes
Soft, mobile, painless subcutaneous mass (back, shoulders)
Rarely becomes malignant
Well-differentiated/dedifferentiated: MDM2 amplification · myxoid: t(12;16)
Adults 50–60; deep thigh or retroperitoneum; lipoblasts with scalloped nuclei
Retroperitoneal fatty mass → liposarcoma
Rhabdomyosarcoma
most common childhood sarcoma
Skeletal muscle differentiation; desmin, myogenin, MyoD1
Embryonal: young children, head/neck, GU (sarcoma botryoides) · alveolar: adolescents, extremities, t(2;13) PAX3-FOXO1
Alveolar has worse prognosis
Smooth muscle; complex karyotype
Retroperitoneum, uterus, large veins (IVC); older adults
Desmin, SMA ⁺
Not from synovium; t(X;18) SS18-SSX
Adults 20–40; deep mass near large joints (knee); biphasic (epithelial + spindle) or monophasic
Keratin, TLE1 ⁺
Undifferentiated pleomorphic sarcoma
No line of differentiation; diagnosis of exclusion
Older adults; deep thigh mass; highly pleomorphic cells
Radiation-associated
Desmoid tumor (aggressive fibromatosis)
Fibroblast clonal proliferation; CTNNB1 (β-catenin) or APC (Gardner)
Abdominal wall in young/postpartum women, mesentery (after surgery in FAP); infiltrative
Recurs locally, doesn't metastasize · nuclear β-catenin
Self-limited reactive/clonal proliferation; USP6 fusion
Young adults; rapidly growing painful forearm nodule over weeks
Fast growth but benign
Schwannoma (encapsulated) · neurofibroma (NF1, plexiform) · MPNST
S100 ⁺; plexiform neurofibroma can turn into MPNST (pain, rapid growth)
NF1 → MPNST risk
ETV6-NTRK3 fusion
Infants; rapidly growing limb mass
TRK inhibitors (larotrectinib)
Mostly hematogenous
Lungs most common; lymph nodes in a few (synovial, rhabdomyosarcoma, clear cell, epithelioid, angiosarcoma)
Chest CT for staging