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Primary Biliary Cirrhosis-Autoimmune Hepatitis Overlap Syndrome.
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Original Article Primary Biliary Cirrhosis-Autoimmune Hepatitis Overlap Syndrome.
Jong Yup Bae, Young Nyun Park, Chanil Park
Journal of Pathology and Translational Medicine 1997;31(1):87-90
DOI: https://doi.org/
Department of Pathology, Yonsei University College of Medicine, Seoul 120-752, Korea.
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Cases sharing features of both primary biliary cirrhosis and autoimmune hepatitis have been reported as a mixed type, overlap syndrome, immunocholangitis and autoimmune cholangiopathy. A primary biliary cirrhosis- autoimmune hepatitis overlap syndrome is unusual and characterized by overlapping features; cholestasis, high titer of alkaline phosphatase, bile duct damage and granulomas in the liver biopsy, high antinuclear antibody, increased IgG and IgM and intra-acinar hepatitis with piecemeal necrosis. Autoimmune mechanisms are thought to play a major role in the pathogenesis of the overlapping syndrome and the bases of immunosuppressive therapy. A 58-year-old female patient shows overlapping clinical and laboratory findings, chronic active hepatitis in initial liver biopsy which transits to primary biliary cirrhosis with cholangitis and granulomas. This is a case of hepatobiliary lesion showing overlapping features of both primary biliary cirrhosis and autoimmune hepatitis over 3-year period.

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