原发性胆汁性胆管炎:机遇与挑战

王绮夏; 马雄

doi:10.3969/j.issn.1001-5256.2017.11.001

原发性胆汁性胆管炎:机遇与挑战

DOI: 10.3969/j.issn.1001-5256.2017.11.001

王绮夏,
马雄

上海交通大学医学院附属仁济医院消化内科上海市消化疾病研究所

基金项目:

国家杰出青年科学基金(81325002)；国家自然科学基金国际合作与交流项目(81620108002);国家自然科学基金面上项目(81570511,81770564)；上海市卫生计生系统“优秀青年医学人才培养计划”(2017YQ037)；

详细信息

中图分类号: R575.22
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- 文章访问数: 315
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- 被引次数: 0
出版历程
- 收稿日期: 2017-10-11
- 出版日期: 2017-11-20

Primary biliary cholangitis:opportunities and challenges

Department of Gastroenterology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Institute of Digestive Disease

Research funding:

摘要

摘要: 原发性胆汁性胆管炎是一种累及肝小叶间胆管的自身免疫性肝病,可进展为肝硬化、肝功能衰竭。早期诊断和治疗可显著改善患者预后,提高生活质量。将2017年欧洲肝病学会《原发性胆汁性胆管炎临床实践指南》与实际临床经验相结合,重点评述我国原发性胆汁性胆管炎研究取得的进展和遇到的难点问题。
- 胆管炎,胆汁性 /
- 诊断 /
- 治疗 /
- 述评
Abstract: Primary biliary cholangitis (PBC) is an autoimmune liver disease mainly involving the interlobular bile ducts and can progress to liver cirrhosis and liver failure.Early diagnosis and management can significantly improve the prognosis of such patients and their quality of life.This article focuses on the achievements of PBC research and related difficult issues in China, with reference to the clinical practice guidelines for PBC by European Association for the Study of the Liver in 2017 and experience in clinical practice.
- cholangitis, biliary /
- diagnosis /
- therapy /
- editorial

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参考文献(13)

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