A Review of IgG4-related Sclerosing Cholangitis (IgG4-SC)

被引:2
|
作者
Khoury, Neil C. [1 ]
Birk, John W. [1 ]
机构
[1] Univ Connecticut Hlth, Div Gastroenterol & Hepatol, Farmington, CT 06030 USA
关键词
autoimmune cholangiopathy; IgG4; cholangiopathy; IgG4-associated autoimmune cholangiopathy; IgG4-related sclerosing cholangitis; AUTOIMMUNE PANCREATITIS; DIAGNOSIS; DISEASE; BILE;
D O I
10.1097/MCG.0000000000001984
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
IgG4-related sclerosing cholangitis (IgG4-SC) is a unique, steroid-responsive, fibroinflammatory condition that is more commonly found in older men and is strongly associated with autoimmune pancreatitis (AIP). It may pose a diagnostic challenge at times due to closely mimicking hepatobiliary diseases such as primary sclerosing cholangitis (PSC), secondary sclerosing cholangitis (SSC), and cholangiocarcinoma. IgG4-SC has an excellent prognosis when promptly diagnosed and treated with steroids. Literature search strategy: The authors searched PubMed and Google Scholar, for articles with the search terms "autoimmune cholangiopathy" and "IgG4 cholangiopathy."
引用
收藏
页码:963 / 969
页数:7
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