Suppr超能文献

胆管颗粒细胞瘤:一种鲜为人知的可治愈的年轻人胆管肿瘤。

Biliary granular cell tumor: a little-known curable bile duct neoplasm of young people.

作者信息

Butterly L F, Schapiro R H, LaMuraglia G M, Warshaw A L

机构信息

Department of Medicine, Harvard Medical School, Boston, Mass.

出版信息

Surgery. 1988 Mar;103(3):328-34.

PMID:2830680
Abstract

Two granular cell tumors of the biliary tree are described, one in a 37-year-old black woman with obstructive jaundice and the other in a 26-year-old white woman with abdominal pain. These are rare soft tissue tumors that have an excellent prognosis when surgically excised. Almost all reported cases have been in young women, the majority of whom have been black. Because granular cell tumors of the biliary tract are uniformly resectable and curable, they should be considered and distinguished from cholangiocarcinoma or localized sclerosing cholangitis, particularly if the patient is young, female, and black.

摘要

本文描述了两例胆管颗粒细胞瘤,一例发生在一名37岁患有梗阻性黄疸的黑人女性身上,另一例发生在一名26岁患有腹痛的白人女性身上。这些是罕见的软组织肿瘤,手术切除后预后良好。几乎所有报道的病例都发生在年轻女性中,其中大多数是黑人。由于胆管颗粒细胞瘤均可切除且可治愈,因此应予以考虑,并与胆管癌或局限性硬化性胆管炎相鉴别,特别是当患者为年轻女性且为黑人时。

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