Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology
- PMID: 35230735
- DOI: 10.1111/liv.15217
Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology
Abstract
Background & aims: Diagnostic histological criteria for autoimmune hepatitis (AIH) have not been clearly established. Previously published criteria focused mainly on chronic AIH, in which inflammatory changes mainly occur in portal/periportal regions and may not be applicable to acute presentation of AIH, in which inflammatory changes are typically predominantly lobular in location. International consensus criteria for the diagnosis and assessment of disease severity in both acute and chronic AIH are thus urgently needed.
Methods: Seventeen expert liver pathologists convened at an international workshop and subsequently used a modified Delphi panel approach to establish consensus criteria for the histopathological diagnosis of AIH.
Results: The consensus view is that liver biopsy should remain standard for diagnosing AIH. AIH is considered likely, if there is a predominantly portal lymphoplasmacytic hepatitis with more than mild interface activity and/or more than mild lobular hepatitis in the absence of histological features suggestive of another liver disease. AIH is also considered likely if there is predominantly lobular hepatitis with or without centrilobular necroinflammation and at least one of the following features: portal lymphoplasmacytic hepatitis, interface hepatitis or portal-based fibrosis, in the absence of histological features suggestive of another liver disease. Emperipolesis and hepatocellular rosettes are not regarded as being specific for AIH.
Conclusions: The criteria proposed in this consensus statement provide a uniform approach to the histological diagnosis of AIH, which is relevant for patients with an acute as well as a chronic presentation and to more accurately reflect the current understanding of liver pathology in AIH.
Keywords: autoimmune hepatitis; histology; lobular hepatitis; portal hepatitis.
© 2022 The Authors. Liver International published by John Wiley & Sons Ltd.
Comment in
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Reassessement of the histological features of autoimmune hepatitis.Liver Int. 2022 May;42(5):954-956. doi: 10.1111/liv.15219. Liver Int. 2022. PMID: 35447009 No abstract available.
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Histological spectrum of autoimmune hepatitis-reply to Fujiwara K. et al.Liver Int. 2022 Jul;42(7):1704-1705. doi: 10.1111/liv.15318. Epub 2022 May 26. Liver Int. 2022. PMID: 35596925 No abstract available.
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Histological re-evaluation of autoimmune hepatitis with acute presentation.Liver Int. 2022 Aug;42(8):1916-1917. doi: 10.1111/liv.15317. Epub 2022 May 27. Liver Int. 2022. PMID: 35596928 No abstract available.
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Histologic criteria of autoimmune hepatitis: Is there anything left to discuss?Liver Int. 2022 Nov;42(11):2587-2588. doi: 10.1111/liv.15391. Epub 2022 Aug 18. Liver Int. 2022. PMID: 35946048 No abstract available.
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Recommendations for histological criteria of autoimmune hepatitis from the international AIH pathology: Validation on a monocentric cohort.Liver Int. 2022 Nov;42(11):2583-2584. doi: 10.1111/liv.15394. Epub 2022 Aug 23. Liver Int. 2022. PMID: 35962757 No abstract available.
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