Suppr超能文献

两性母细胞瘤。一例罕见卵巢肿瘤的报告及文献综述

Gynandroblastoma. Report of an unusual ovarian tumour and literature review.

作者信息

Limaïem F, Lahmar A, Ben Fadhel C, Bouraoui S, M'zabi-Regaya S

机构信息

Department of Pathology, Mongi Slim Hospital, Sidi Daoued La Marsa (2046), Tunisia.

出版信息

Pathologica. 2008 Feb;100(1):13-7.

Abstract

Gynandroblastoma is a rare variant of ovarian sex cord stromal tumours that demonstrates morphological evidence of both male and female differentiation. We report a new case of gynandroblastoma in a 22-year-old nulliparous female with a history of menstrual disturbance. Physical examination disclosed a painless pelvic mass measuring 20 cm across with normal secondary sex characteristics, and no signs of virilisation. Histological examination of the surgically resected primary tumour revealed a predominant adult granulosa cell component admixed with a minor Sertoli cell component that did not exceed 20% of the tumour. Immunohistochemical analysis showed positive immunostaining of Sertoli cell areas with inhibin. The final diagnosis was gynandroblastoma. The post-operative course was uneventful and there was no evidence of recurrence during the 9-month follow-up period.

摘要

两性母细胞瘤是卵巢性索间质肿瘤的一种罕见变异型,具有男性和女性分化的形态学证据。我们报告一例22岁未生育女性的两性母细胞瘤新病例,该患者有月经紊乱病史。体格检查发现一个直径20厘米的无痛性盆腔肿块,第二性征正常,无男性化体征。对手术切除的原发肿瘤进行组织学检查,发现主要为成年颗粒细胞成分,混合有少量不超过肿瘤20%的支持细胞成分。免疫组织化学分析显示支持细胞区域抑制素免疫染色呈阳性。最终诊断为两性母细胞瘤。术后过程顺利,在9个月的随访期内无复发迹象。

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