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Clinical and pathological studies on the autoimmune hepatitis and primary biliary cirrhosis overlap syndrome :an analysis of 16 cases

Zhihong Liu

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Abstract

Objective To explore the clinical and pathological features and responses to therapy of autoimmune hepatitis and primary biliary cirrhosis overlap syndrome. Methods We included 16 cases with AIH-PBC overlap syndrome, 26 with type I AIH and 25 with PBC (Scheuer stage Ⅰand Ⅱ) , and the emphasis was laid upon the clinical manifestations , pathological features and responses to therapy. Results No significant differences in sex , age and course of diseases were found among the 3 groups. In AIH-PBC group , the serum levels of alkaline phosphatase,γ-glutamyltranspeptidase, IgM and the frequency of positive antimitochondrial antibodies and AMA-M2 were significantly higher than in the AIH type one group ( P 0.05); and the levels of alanine transaminase, aspartic transaminase,γ-globulin and IgG and the presence of positive antinuclear antibody or antismooth muscle antibody were markedly higher than those in PBC group ( P0.05) . The liver biopsy specimens in the AIH-PBC group were characterized by interface hepatitis , piecemeal necrosis and bile duct lesion. UDCA treatment can improve liver function tests in AIH-PBC patients. Conclusion A combined features of both AIH and PBC exists in overlap syndrome. The administration of UDCA may get benefit.

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Objective To explore the clinical and pathological features and responses to therapy of autoimmune hepatitis and primary biliary cirrhosis overlap syndrome. Methods We included 16 cases with AIH-PBC overlap syndrome, 26 with type I AIH and 25 with PBC (Scheuer stage Ⅰand Ⅱ) , and the emphasis was laid upon the clinical manifestations , pathological features and responses to therapy. Results No significant differences in sex , age and course of diseases were found among the 3 groups. In AIH-PBC group , the serum levels of alkaline phosphatase,γ-glutamyltranspeptidase, IgM and the frequency of positive antimitochondrial antibodies and AMA-M2 were significantly higher than in the AIH type one group ( P 0.05); and the levels of alanine transaminase, aspartic transaminase,γ-globulin and IgG and the presence of positive antinuclear antibody or antismooth muscle antibody were markedly higher than those in PBC group ( P0.05) . The liver biopsy specimens in the AIH-PBC group were characterized by interface hepatitis , piecemeal necrosis and bile duct lesion. UDCA treatment can improve liver function tests in AIH-PBC patients. Conclusion A combined features of both AIH and PBC exists in overlap syndrome. The administration of UDCA may get benefit.

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Available abstract

Objective To explore the clinical and pathological features and responses to therapy of autoimmune hepatitis and primary biliary cirrhosis overlap syndrome. Methods We included 16 cases with AIH-PBC overlap syndrome, 26 with type I AIH and 25 with PBC (Scheuer stage Ⅰand Ⅱ) , and the emphasis was laid upon the clinical manifestations , pathological features and responses to therapy. Results No significant differences in sex , age and course of diseases were found among the 3 groups. In AIH-PBC group , the serum levels of alkaline phosphatase,γ-glutamyltranspeptidase, IgM and the frequency of positive antimitochondrial antibodies and AMA-M2 were significantly higher than in the AIH type one group ( P 0.05); and the levels of alanine transaminase, aspartic transaminase,γ-globulin and IgG and the presence of positive antinuclear antibody or antismooth muscle antibody were markedly higher than those in PBC group ( P0.05) . The liver biopsy specimens in the AIH-PBC group were characterized by interface hepatitis , piecemeal necrosis and bile duct lesion. UDCA treatment can improve liver function tests in AIH-PBC patients. Conclusion A combined features of both AIH and PBC exists in overlap syndrome. The administration of UDCA may get benefit.

Key concepts: Medicine, Autoimmune hepatitis, Primary biliary cirrhosis, Overlap syndrome, Pathological, Internal medicine, Anti-nuclear antibody, Liver biopsy

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