Myxoid liposarcoma
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A myxoid liposarcoma is a malignant adipose tissue neoplasm[1] of myxoid appearance histologically.
Myxoid liposarcomas are the second most common type of liposarcoma, representing 30%–40% of all liposarcomas in the limbs; occurring most commonly in the legs, particularly the thigh, followed by the buttocks, retroperitoneum, trunk, ankle, proximal limb girdle, head and neck, and wrist. They occur in the intermuscular fascial planes or deep-seated areas. They present as a large, slow-growing, painless mass.[2]
They are associated with a fusion between DDIT3 or "CHOP" (at 12q13.1-q13.2) and FUS or "TLS" (at 16p11.2) or EWS (at 22q12.2).[3] [4] [5] The specific translocation of FUS-DDIT3 is t(12;16)(q13;p11).[6] [7]
See also
Further reading
- Myxoid liposarcoma: a rare soft-tissue tumor with a misleading benign appearance
- Efficacy of first-line doxorubicin and ifosfamide in myxoid liposarcoma. 2012
References
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- ↑ Myxoid/round cell liposarcoma
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