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Title: Portal Hypertensive Biliopathy as a Cause of Severe Cholestasis in Children With Congenital Hepatic Fibrosis. Author: Dalgıç A, Sarı S, Sözen MH, Gürcan Kaya N, Dalgıç B. Journal: Exp Clin Transplant; 2019 Jan; 17(Suppl 1):223-225. PubMed ID: 30777560. Abstract: Portal hypertensive biliopathy may occur in patients with noncirrhotic hepatic fibrosis. Portal hypertensive biliopathy treatment should be focused on management of portal hypertension and relief of biliary obstruction. In patients with noncirrhotic portal fibrosis and symptomatic portal hypertensive biliopathy, portal decompression surgery by proximal splenorenal shunt is one successful treatment option.[Abstract] [Full Text] [Related] [New Search]