10.22376/ijpbs.2019.10.1.p1-12 Volume 6 Issue 4 2015 (October - December) Autoimmune cholangitis has recently been described as a rare, chronic cholestatic liver disease with clinical, biochemical, and immunological features of both primary and autoimmune hepatitis (CAH) and cholestasis with raised Ig G4 levels. In autoimmunecholangitis, increased levels ofγ- glutamyl transferase (GGT) and alkaline phophatase (AP) are disproportionate in comparison with the elevation in transaminases (AST/ALT), suggesting cholestatic liverdisease.We present a 34 year old female who presented with features of chronic hepatitis with pruritus which turned out to be Auto immune cholangitis (AIC). DR. SAKTHI SELVA KUMAR, DR. VINOTH KUMAR, DR. BALAKISHNAN AND DR.N.N.ANAND Cholestasis, chronic hepatitis, autoimmune cholangitis. 360-365