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青年原发性卵巢癌肉瘤1例临床分析
引用本文:刘忠宇,赵恩锋,刘春红,乔江丽,李晨星. 青年原发性卵巢癌肉瘤1例临床分析[J]. 河北医学, 2012, 18(1): 66-69
作者姓名:刘忠宇  赵恩锋  刘春红  乔江丽  李晨星
作者单位:中国人民解放军总医院妇产科,北京,100853
摘    要:目的:提高对青年原发性卵巢癌肉瘤的认识,探讨原发性卵巢癌肉瘤的临床特点、诊断及治疗。方法:报道1例青年原发性卵巢癌肉瘤,并复习相关文献。结果:原发性卵巢癌肉瘤可伴有CA125的升高,多以消化道症状起病,预后差进展迅速,目前主要以手术治疗为主,没有有效的化疗方案。结论:原发性卵巢癌肉瘤为恶性混合性中胚层肿瘤中的一种,临床罕见,高度恶性,特异性临床表现少,病理活检为确诊手段,多见于绝经后妇女,30岁以前发病者罕见,预后差生存率低。

关 键 词:卵巢癌肉瘤  青年  中胚层肿瘤

Clinical Analysis of one Case Youth Primary Ovarian Carcinosarcoma
Affiliation:LIU Zhongyu,ZHAO Enfeng,LIU Chunhong,et al(The General Hospital of People’s Liberation Army,Beijing 100853,China)
Abstract:Objective: To improve the understanding of youth primary ovarian carcinosarcoma,and explore the clinical features,diagnosis and therapy of ovarian carcinosarcoma.Method: A case report of youth primary ovarian carcinosarcoma and review relative literatures.Result:Primary ovarian carcinosarcoma may be associated with elevated CA125,mostly gastrointestinal symptoms onset,poor prognosis and rapid progress,Present mainly treatment is surgery and there is no effective on chemotherapy.Conclusion: Primary ovarian carcinosarcoma is a kind of rare,highly aggressive and highly malignant tumor,it is a variety of the mixed malignant mesodermal tumors.Mainly seen in postmenopausal women,30 were extremely rare before the age of onset.Poor progress and low survival rate.
Keywords:Youth  Ovarian carcinosarcoma  Mesodermal tumor
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