Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group

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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. / Lohse, Ansgar W; Sebode, Marcial; Bhathal, Prithi S; Clouston, Andrew D; Dienes, Hans P; Jain, Dhanpat; Gouw, Annette S H; Guindi, Maha; Kakar, Sanjay; Kleiner, David E; Krech, Till; Lackner, Carolin; Longerich, Thomas; Saxena, Romil; Terracciano, Luigi; Washington, Kay; Weidemann, Sören; Hübscher, Stefan G; Tiniakos, Dina.

in: LIVER INT, Jahrgang 42, Nr. 5, 05.2022, S. 1058-1069.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Lohse, A. W., Sebode, M., Bhathal, P. S., Clouston, A. D., Dienes, H. P., Jain, D., Gouw, A. S. H., Guindi, M., Kakar, S., Kleiner, D. E., Krech, T., Lackner, C., Longerich, T., Saxena, R., Terracciano, L., Washington, K., Weidemann, S., Hübscher, S. G., & Tiniakos, D. (2022). 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. LIVER INT, 42(5), 1058-1069. https://doi.org/10.1111/liv.15217

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@article{9a08ff309df14d25bb3047162a5a27b5,
title = "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",
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 = "Biopsy, Hepatitis, Autoimmune, Humans, Liver/pathology, Severity of Illness Index",
author = "Lohse, {Ansgar W} and Marcial Sebode and Bhathal, {Prithi S} and Clouston, {Andrew D} and Dienes, {Hans P} and Dhanpat Jain and Gouw, {Annette S H} and Maha Guindi and Sanjay Kakar and Kleiner, {David E} and Till Krech and Carolin Lackner and Thomas Longerich and Romil Saxena and Luigi Terracciano and Kay Washington and S{\"o}ren Weidemann and H{\"u}bscher, {Stefan G} and Dina Tiniakos",
note = "{\textcopyright} 2022 The Authors. Liver International published by John Wiley & Sons Ltd.",
year = "2022",
month = may,
doi = "10.1111/liv.15217",
language = "English",
volume = "42",
pages = "1058--1069",
journal = "LIVER INT",
issn = "1478-3223",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group

T2 - Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology

AU - Lohse, Ansgar W

AU - Sebode, Marcial

AU - Bhathal, Prithi S

AU - Clouston, Andrew D

AU - Dienes, Hans P

AU - Jain, Dhanpat

AU - Gouw, Annette S H

AU - Guindi, Maha

AU - Kakar, Sanjay

AU - Kleiner, David E

AU - Krech, Till

AU - Lackner, Carolin

AU - Longerich, Thomas

AU - Saxena, Romil

AU - Terracciano, Luigi

AU - Washington, Kay

AU - Weidemann, Sören

AU - Hübscher, Stefan G

AU - Tiniakos, Dina

N1 - © 2022 The Authors. Liver International published by John Wiley & Sons Ltd.

PY - 2022/5

Y1 - 2022/5

N2 - 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.

AB - 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.

KW - Biopsy

KW - Hepatitis, Autoimmune

KW - Humans

KW - Liver/pathology

KW - Severity of Illness Index

U2 - 10.1111/liv.15217

DO - 10.1111/liv.15217

M3 - SCORING: Journal article

C2 - 35230735

VL - 42

SP - 1058

EP - 1069

JO - LIVER INT

JF - LIVER INT

SN - 1478-3223

IS - 5

ER -