医学
原发性硬化性胆管炎
溃疡性结肠炎
炎症性肠病
疾病
炎症性肠病
克罗恩病
胃肠病学
内科学
作者
Alireza Beheshti‐Maal,Atena Tamimi,Shahrokh Iravani,Arash Memarnejadian,Majid Sorouri,Hamid Asadzadeh Aghdaei,Mohammad Reza Zali,Nikoo Hossein‐Khannazer,Massoud Vosough
标识
DOI:10.1080/17474124.2022.2031979
摘要
Primary sclerosing cholangitis (PSC) is a rare, chronic, and progressive cholestatic disease involving intra- and/or extrahepatic bile ducts. PSC in many patients results in end-stage liver diseases. Nearly 60% of the PSC patients suffer from concomitant inflammatory bowel diseases (IBDs). Classically, IBDs are divided into two principle types: Crohn's disease (CD) and ulcerative colitis (UC). However, with growing knowledge, PSC-associated IBD (PSC-IBD) seems to be a rather distinct entity with specific genetics, clinical, and microbiota characteristics.In this article, we aim to review the unique characteristics of PSC-IBD from clinical, genetic, and microbiota point of view.PSC-IBD's unique characteristics contribute to the notion that it could be a distinct entity. Acknowledgment of PSC-IBD as a novel entity necessitates designing new clinical guidelines for diagnosis and developing novel therapies.
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