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Epithelioid Angiosarcoma in a Patient with Klippel-Trénaunay-Weber Syndrome: An Unexpected Response to Therapy
Angela Simas1, Catarina Matos, Rodrigo Lopes da Silva
1Serviço de Medicina Interna 3, Hospital Santo António dos Capuchos.
Case Reports in Oncology
|August 27, 2010
Abstract:
We present a rare case of Stewart-Treves syndrome characterized by a diffuse angiosarcoma of the leg in a 22-year-old man with a history of chronic lymphedema due to Klippel-Trénaunay-Weber syndrome. He underwent limb disarticulation and medical treatment with cycles of doxorubicin, oral thalidomide and sunitinib with a very good response after 12 months of follow-up.