原发性胆汁性肝硬化并空肠间质瘤1例报道  

Primary biliary cirrhosis with jejunal stromal tumor:one case report

作　　者：赵亚亚 肖萍[2] 赵正斌[3] ZHAO Yaya;XIAO Ping;ZHAO Zhengbin(The First Clinical Medical College of Lanzhou University,Lanzhou 730000;Laboratory of Infections Diseases,the First Hospital of Lanzhou University;Department of Infectious Disease,the First Hospital of Lanzhou University,China)

机构地区：[1]兰州大学第一临床医学院,甘肃兰州730000 [2]兰州大学第一医院传染病研究室 [3]兰州大学第一医院感染科

出　　处：《胃肠病学和肝病学杂志》2018年第12期1392-1394,共3页Chinese Journal of Gastroenterology and Hepatology

摘　　要：原发性胆汁性肝硬化(primary biliary cirrhosis,PBC)是一种以胆汁淤积为特点的慢性自身免疫性肝病,常于疾病早期即可出现严重的门静脉高压。胃肠道间质瘤(gastrointestinal stromal tumour,GIST)因缺乏典型的症状,往往在其他疾病的诊疗过程中发现,首选手术治疗,门静脉高压通常增加了手术难度。本文报道了1例PBC合并空肠间质瘤的诊疗过程,供临床医师参考。Primary biliary cirrhosis(PBC) is a chroic inflammatory autoimmune cholsetatic liver disease,which can occur severe portal hypertension in the early stage of disease.Gastrointestinal stromal tumor(GIST) are often found in the diagnosis and treatment of other diseases due to lack of typical symptoms,surgical resection is the primary treatment for GIST.Portal hypertension usually increases the difficulty of surgery.The paper reported one case of PBC with jejunal stromal tumor for clinical reference.

关 键 词：胆汁性肝硬化 空肠间质瘤 病例报道 

分 类 号：R575.5[医药卫生—消化系统]