Suppr超能文献

大网膜原发性内胚窦瘤

Primary endodermal sinus tumor of the omentum.

作者信息

Park N H, Ryu S Y, Park I A, Kang S B, Lee H P

机构信息

College of Medicine, Seoul National University, Seoul, 110-744, Korea.

出版信息

Gynecol Oncol. 1999 Mar;72(3):427-30. doi: 10.1006/gyno.1998.5268.

Abstract

Endodermal sinus tumor (EST) is a rare neoplasm which usually arises in the testis or ovary. But extragonadal EST is well recognized and may arise in a wide array of sites such as the mediastinum, vagina, and brain. We report a case of primary EST of the omentum and to our knowledge it is the first case of omental EST in the literature. A 45-year-old woman with a history of abdominal distension was treated with total abdominal hysterectomy with bilateral salpingo-oophorectomy and infracolic omentectomy, followed by four cycles of BEP (bleomycin, etoposide, cisplatin) combination chemotherapy. Microscopically, the tumor exhibited typical patterns of EST and stained for alpha-fetoprotein and cytokeratin. She has remained free of disease for 10 months of follow-up. According to previous studies, debulking surgery and BEP chemotherapy were used as primary therapy with good results. The subject of extragonadal EST is reviewed, and the possible histogenesis of this tumor at such a rare site is discussed.

摘要

内胚窦瘤(EST)是一种罕见的肿瘤,通常发生于睾丸或卵巢。但性腺外EST已得到充分认识,可发生于多种部位,如纵隔、阴道和脑。我们报告一例大网膜原发性EST,据我们所知,这是文献中首例大网膜EST病例。一名有腹胀病史的45岁女性接受了全腹子宫切除术、双侧输卵管卵巢切除术和结肠下大网膜切除术,随后进行了四个周期的BEP(博来霉素、依托泊苷、顺铂)联合化疗。显微镜下,肿瘤呈现出EST的典型形态,并对甲胎蛋白和细胞角蛋白呈阳性染色。随访10个月,她仍无疾病复发。根据以往研究,肿瘤细胞减灭术和BEP化疗作为主要治疗方法效果良好。本文对内胚窦瘤进行了综述,并探讨了该肿瘤在如此罕见部位可能的组织发生。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验