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Stewart–Treves syndrome
Stewart–Treves syndrome, also known as Cutaneous angiosarcoma, refers to a lymphangiosarcoma, a rare complication that forms as a result of chronic, long-standing lymphedema. Although it most commonly refers to malignancies associated with chronic lymphedema resulting from mastectomy and/or radiotherapy for breast cancer, it may also describe lymphangiosarcomas that result from congenital and other causes of chronic secondary lymphedema. Lymphangiosarcoma arising from cancer-related lymphedema has become much less common with better surgical techniques, radiation therapy, and conservative treatment. The prognosis, even with wide surgical excision and subsequent radiotherapy, is poor.
== History==
It was discovered by Fred W. Stewart and Norman Treves in 1948.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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