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1例复发卵巢血管肉瘤治疗后妊娠的病例报道与文献回顾 被引量:1
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作者 Jha S. chan k.k. +2 位作者 Poole C.J. Rollason T.P. 李跃萍 《世界核心医学期刊文摘(妇产科学分册)》 2005年第12期43-43,共1页
Background. Ovarian angiosarcomas are rare tumors which may to be distinguished from other unusual primary ovarian tumors such as clear cell carcinoma, yolk sac tumor and leiomyosarcoma on the basis of histological ap... Background. Ovarian angiosarcomas are rare tumors which may to be distinguished from other unusual primary ovarian tumors such as clear cell carcinoma, yolk sac tumor and leiomyosarcoma on the basis of histological appearance and immunohistochemistry. Angiosarcomas of the ovary occur in all age groups but are more frequent in women of child bearing age (less than 40 years). Surgery and radiotherapy have been the traditional treatment modalities. Case. The case we present is the only reported long-term survivor of recurrent ovarian angiosarcoma. Her initial treatment was surgical, both at presentation and relapse but since she wished conservation of fertility, radical surgery and radiotherapy were avoided and she underwent further adjuvant chemotherapy with doxorubicin and ifosfamide. She remains in remission 6 years after treatment of recurrence of the primary tumor and has had a successful pregnancy following treatment. Conclusion. Adjuvant chemotherapy of ovarian angiosarcoma with a combination of doxorubicin and ifosfamide appears effective and should be considered in women at risk of relapse who wish to conserve fertility. 展开更多
关键词 卵巢血管肉瘤 文献回顾 卵黄囊瘤 异磷酰胺 辅助性化疗 透明细胞癌 平滑肌肉瘤 根治性手术 联合放疗 复发风险
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