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Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis

BACKGROUND AND AIM: Centrilobular zonal necrosis (CZN) is a known histological variant of autoimmune hepatitis (AIH). However, the significance of CZN is yet to be fully elucidated. This study aimed to determine whether CZN is a hallmark of a distinctive subtype of AIH. METHODS: Histological changes...

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Autores principales: Aizawa, Yoshio, Abe, Hiroshi, Sugita, Tomonori, Seki, Nobuyoshi, Chuganji, Yoshimichi, Furumoto, Youhei, Sakata, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams And Wilkins 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777223/
https://www.ncbi.nlm.nih.gov/pubmed/26657454
http://dx.doi.org/10.1097/MEG.0000000000000545
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author Aizawa, Yoshio
Abe, Hiroshi
Sugita, Tomonori
Seki, Nobuyoshi
Chuganji, Yoshimichi
Furumoto, Youhei
Sakata, Akihiko
author_facet Aizawa, Yoshio
Abe, Hiroshi
Sugita, Tomonori
Seki, Nobuyoshi
Chuganji, Yoshimichi
Furumoto, Youhei
Sakata, Akihiko
author_sort Aizawa, Yoshio
collection PubMed
description BACKGROUND AND AIM: Centrilobular zonal necrosis (CZN) is a known histological variant of autoimmune hepatitis (AIH). However, the significance of CZN is yet to be fully elucidated. This study aimed to determine whether CZN is a hallmark of a distinctive subtype of AIH. METHODS: Histological changes in the centrilobular zones of liver biopsies from 113 AIH patients were assessed by a single pathologist and classified into three categories: typical zonal necrosis defined as CZN (15 patients); other necroinflammatory change (NIC; 24 patients); and absence of necrosis (non-NIC; 74 patients). The clinicopathological features and immunogenetic background of CZN patients were then assessed. RESULTS: The clinicopathological features of AIH with CZN were distinct from other types of AIH, including a higher frequency of acute onset, lower frequency of antinuclear antibodies, lower antinuclear antibody titers, lower serum immunoglobulin G levels, lower grade interface hepatitis, less prominent lymphoplasmacytic infiltration, and lower AIH score. Increased and decreased frequencies of HLA-DR9 and HLA-DR4, respectively, were identified as immunogenetic features of AIH with CZN. Conversely, the clinicopathological characteristics of AIH with NIC were similar to those of non-NIC AIH, including the majority of the AIH patients. The therapeutic outcomes of AIH with CZN were excellent when precise diagnoses were made without delay. CONCLUSION: The clinicopathological features and immunogenetic background of AIH with CZN differed from AIH without CZN. CZN may be a hallmark of a distinct subtype of AIH.
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spelling pubmed-47772232016-03-19 Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis Aizawa, Yoshio Abe, Hiroshi Sugita, Tomonori Seki, Nobuyoshi Chuganji, Yoshimichi Furumoto, Youhei Sakata, Akihiko Eur J Gastroenterol Hepatol Original Articles: Hepatitis BACKGROUND AND AIM: Centrilobular zonal necrosis (CZN) is a known histological variant of autoimmune hepatitis (AIH). However, the significance of CZN is yet to be fully elucidated. This study aimed to determine whether CZN is a hallmark of a distinctive subtype of AIH. METHODS: Histological changes in the centrilobular zones of liver biopsies from 113 AIH patients were assessed by a single pathologist and classified into three categories: typical zonal necrosis defined as CZN (15 patients); other necroinflammatory change (NIC; 24 patients); and absence of necrosis (non-NIC; 74 patients). The clinicopathological features and immunogenetic background of CZN patients were then assessed. RESULTS: The clinicopathological features of AIH with CZN were distinct from other types of AIH, including a higher frequency of acute onset, lower frequency of antinuclear antibodies, lower antinuclear antibody titers, lower serum immunoglobulin G levels, lower grade interface hepatitis, less prominent lymphoplasmacytic infiltration, and lower AIH score. Increased and decreased frequencies of HLA-DR9 and HLA-DR4, respectively, were identified as immunogenetic features of AIH with CZN. Conversely, the clinicopathological characteristics of AIH with NIC were similar to those of non-NIC AIH, including the majority of the AIH patients. The therapeutic outcomes of AIH with CZN were excellent when precise diagnoses were made without delay. CONCLUSION: The clinicopathological features and immunogenetic background of AIH with CZN differed from AIH without CZN. CZN may be a hallmark of a distinct subtype of AIH. Lippincott Williams And Wilkins 2016-04 2016-03-09 /pmc/articles/PMC4777223/ /pubmed/26657454 http://dx.doi.org/10.1097/MEG.0000000000000545 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Articles: Hepatitis
Aizawa, Yoshio
Abe, Hiroshi
Sugita, Tomonori
Seki, Nobuyoshi
Chuganji, Yoshimichi
Furumoto, Youhei
Sakata, Akihiko
Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
title Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
title_full Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
title_fullStr Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
title_full_unstemmed Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
title_short Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
title_sort centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis
topic Original Articles: Hepatitis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777223/
https://www.ncbi.nlm.nih.gov/pubmed/26657454
http://dx.doi.org/10.1097/MEG.0000000000000545
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