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World J Hepatol. May 27, 2026; 18(5): 117837
Published online May 27, 2026. doi: 10.4254/wjh.v18.i5.117837
Figure 1
Figure 1 Aminotransferases activity. A: Aminotransferases activity during the patient’s initial hospitalization; B: Aminotransferases activity during the patient’s second hospitalization. ALT: Alanine aminotransferase; AST: Aspartate aminotransferase; U/L: Units per liter.
Figure 2
Figure 2 Pathologic findings of the liver biopsy. A: The portal tracts are infiltrated by lymphocytes, plasma cells and eosinophils. The interface hepatitis is evident; B: Close-up view to portal tract with interface hepatitis and parenchymal hepatitis with the contribution of eosinophils and plasma cells.
Figure 3
Figure 3 A double chromogen assay of immunohistochemistry for CD4 (3,3’-diaminobenzidine, brown colour) and CD8 (red colour). Close to equal contribution of CD4 and CD8 lymphocytes. Numerous CD8+ cytotoxic lymphocytes in the portal tract.
Figure 4
Figure 4 CD138-positive singular and aggregates plasma cells in the portal tract (immunohistochemistry, CD138).
Figure 5
Figure 5 Aminotransferases activity during the nine-month follow-up period and corresponding treatment. ALT: Alanine aminotransferase; AST: Aspartate aminotransferase; U/L: Units per liter.
Figure 6
Figure 6 Simplified algorithm of first-line and subsequent therapeutic management in autoimmune hepatitis (according to European Association for the Study of the Liver Clinical Practice Guidelines, 2025). 1Low-dose predniso(lo)ne monotherapy can be suggested only in patients with mild disease who achieved complete biochemical response and are intolerant to both azathioprine and mycophenolate mofetil. AZP: Azathioprine; MMF: Mycophenolate mofetil; CBR: Complete biochemical response; TG: Thioguanine; TGN: Thioguanine nucleotides; MMP: Methylmercaptopurine.


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