Published online Aug 27, 2023. doi: 10.4254/wjh.v15.i8.939
Peer-review started: May 15, 2023
First decision: July 10, 2023
Revised: July 23, 2023
Accepted: August 11, 2023
Article in press: August 11, 2023
Published online: August 27, 2023
Processing time: 99 Days and 7.5 Hours
Primary sclerosing cholangitis (PSC) is a chronic and progressive immune-mediated cholangiopathy causing biliary tree inflammation and scarring, leading to liver cirrhosis and end-stage liver disease. Diagnosis of PSC is challenging due to its nonspecific symptoms and overlap with other liver diseases. Despite the rising incidence of PSC, there is no proven medical therapy that can alter the natural history of the disease. While liver transplantation (LT) is the most effective approach for managing advanced liver disease caused by PSC, post-transplanta
Core Tip: Despite recent advancements in the field of hepatology, therapeutic options for the medical management of primary sclerosing cholangitis (PSC) are limited. Liver transplantation (LT) remains the primary treatment for patients with end stage liver disease (ESLD) secondary to PSC. Both deceased donor liver transplant and living donor liver transplant have demonstrated successful outcomes in patients with ESLD. Psychosocial patient factors also play a significant role in the outcome LT. Addressing ethical issues is crucial to ensure healthcare equity. Recent developments in digital technology and stem cell therapy suggest a promising future for LT in PSC.
