Suppr超能文献

伴有肉瘤过度生长及此前未报道的MEIS1-NCOA2基因融合的原发性输卵管苗勒管腺肉瘤

Primary Fallopian Tube Mullerian Adenosarcoma With Sarcomatous Overgrowth and a Previously Unreported MEIS1-NCOA2 Gene Fusion.

作者信息

Ribeiro E Ribeiro Renan, Lewin Eleanor R, Hart Jesse L, Quddus Mohammad Ruhul, Hansen Katrine

出版信息

Int J Gynecol Pathol. 2022 Jan 1;41(1):82-85. doi: 10.1097/PGP.0000000000000777.

Abstract

Extrauterine Mullerian adenosarcomas (MA) are rare and often associated with endometriosis. We report a 55-yr-old patient seen in consultation for abdominal pain and bloating. Imaging was suggestive of a left adnexal mass and "peritoneal carcinomatosis". Pathological examination of the specimen revealed a MA arising in the left fallopian tube, with sarcomatous overgrowth, diffuse peritoneal involvement and omental "caking". Next-generation sequencing identified a MEIS1-NCOA2 gene fusion, previously unreported in MA.

摘要

子宫外苗勒管腺肉瘤(MA)罕见,且常与子宫内膜异位症相关。我们报告一例55岁因腹痛和腹胀前来会诊的患者。影像学检查提示左侧附件包块和“腹膜癌病”。标本的病理检查显示左侧输卵管发生了MA,伴有肉瘤样过度生长、弥漫性腹膜受累和网膜“饼状粘连”。二代测序鉴定出一种MEIS1-NCOA2基因融合,此前在MA中未报道过。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验