Published online Feb 18, 2016. doi: 10.4254/wjh.v8.i5.265
Peer-review started: August 6, 2015
First decision: September 16, 2015
Revised: January 13, 2016
Accepted: January 21, 2016
Article in press: January 22, 2016
Published online: February 18, 2016
Processing time: 198 Days and 6.2 Hours
Primary sclerosing cholangitis (PSC) remains a rare but significant disease, which affects mainly young males in association with inflammatory bowel disease. There have been few advances in the understanding of the pathogenesis of the condition and no therapeutics with proven mortality benefit aside from liver transplantation. There remain areas of controversy in the management of PSC which include the differentiation from other cholangiopathies, in particular immunoglobulin G4 related sclerosing cholangitis, the management of dominant biliary strictures, and the role of ursodeoxycholic acid. In addition, the timing of liver transplantation in PSC remains difficult to predict with standard liver severity scores. In this review, we address these controversies and highlight the latest evidence base in the management of PSC.
Core tip: There have been few advances in therapeutics for primary sclerosing cholangitis (PSC) and there remain areas of controversy in the management of PSC. In this review, we address these controversies, which include the differentiation of PSC from other cholangiopathies, in particular immunoglobulin G4 related sclerosing cholangitis, the management of dominant biliary strictures, the role of ursodeoxycholic acid, and the timing of liver transplantation.