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Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease characterized by fibroinflammatory damage to the biliary tree, typically in the setting of inflammatory bowel disease, with an elevated risk of liver failure and cholangiocarcinoma. A complex pathophysiology, heterogeneity in clinical features, and the rare nature of the disease have contributed to the lack of effective therapy to date. However, recent innovations in the characterization and prognostication of patients with PSC, in addition to new tools for medical management and emerging pharmacologic agents, give rise to the potential for meaningful progress in the next several years. This review summarizes current concepts in PSC and highlights areas of particular areas in need of further study.
You can read an interview with the lead study author here, and about the clinical implications of the study here.
Read the full article
Recent Advances in the Management of Primary Sclerosing Cholangitis
Primary Source
Clinical Gastroenterology and Hepatology
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