Komorowski Andrzej L, Wysocki Wojciech M, Mituś Jerzy
Department of Surgical Oncology, Center of Oncology, Maria Curie-Sklodowska Memorial Institute of Oncology, Krakow, Poland.
South Med J. 2003 Aug;96(8):807-8. doi: 10.1097/01.SMJ.0000054692.22369.6E.
Angiosarcoma arising from chronic lymphedema is referred to as Stewart-Treves syndrome. It typically occurs as a complication of long-lasting lymphedema of the arm after mastectomy and/or radiotherapy for breast cancer. Angiosarcoma associated with idiopathic lymphedema of the lower extremity is extremely rare. We report a case of diffuse angiosarcoma of the leg in a patient with a 25-year history of idiopathic lymphedema. Despite rapid aggressive surgical treatment, the patient died 6 weeks after diagnosis.
由慢性淋巴水肿引起的血管肉瘤被称为斯图尔特-特里夫斯综合征。它通常是乳腺癌乳房切除术后和/或放疗后手臂长期淋巴水肿的并发症。与下肢特发性淋巴水肿相关的血管肉瘤极为罕见。我们报告一例患有25年特发性淋巴水肿病史的患者发生腿部弥漫性血管肉瘤的病例。尽管进行了积极迅速的手术治疗,但患者在诊断后6周死亡。