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伴有卡波西样血管内皮瘤病的血管肉瘤:两例紫杉醇治疗病例报告。

Angiosarcoma associated with a Kasabach-Merritt syndrome: report of two cases treated with paclitaxel.

机构信息

Department of Medical Oncology, Institut Bergonié, Bordeaux, France.

出版信息

Future Oncol. 2013 Sep;9(9):1397-9. doi: 10.2217/fon.13.109.

Abstract

Angiosarcomas are rare, aggressive vascular malignancies of endothelial cell differentiation. Kasabach-Merritt syndrome is a rare condition defined by the association of thrombocytopenia and consumption coagulopathy with specific vascular tumors, such as tufted angioma or kaposiform hemangioendothelioma. We report here two cases of angiosarcomas complicated by a Kasabach-Merritt syndrome and their outcome after treatment with paclitaxel.

摘要

血管肉瘤是一种罕见的、具有侵袭性的血管内皮细胞分化来源的恶性肿瘤。卡波西肉瘤-梅里特(Kasabach-Merritt)综合征是一种罕见的疾病,其特征是血小板减少和消耗性凝血病与特定的血管肿瘤(如丛状血管瘤或卡波西样血管内皮细胞瘤)相关。我们在此报告两例血管肉瘤合并卡波西肉瘤-梅里特(Kasabach-Merritt)综合征的病例,并报道了他们在紫杉醇治疗后的结局。

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