Cunningham M J, Brooks J S, Noumoff J S
Department of Obstetrics and Gynecology, Hospital of the University of Pennsylvania, Philadelphia 19104.
Gynecol Oncol. 1994 May;53(2):265-8. doi: 10.1006/gyno.1994.1128.
Angiosarcoma originating in the female genital tract is exceedingly rare with only 15 cases of angiosarcoma of the ovary described to date. All have been highly aggressive tumors, and no response to treatment has ever been reported. A case of primary ovarian angiosarcoma is described in which a short remission was achieved with intensive chemotherapy using ifosfamide and doxorubicin.
起源于女性生殖道的血管肉瘤极为罕见,迄今为止仅有15例卵巢血管肉瘤的报道。所有病例均为高度侵袭性肿瘤,且从未有过对治疗有反应的报道。本文描述了一例原发性卵巢血管肉瘤病例,该病例通过使用异环磷酰胺和阿霉素的强化化疗实现了短期缓解。