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A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis

Both autoimmune hepatitis (AIH) and eosinophilic fasciitis (EF) are known to be complicated by other autoimmune diseases. However, AIH complicated by EF has never been reported. We experienced a 58-year-old man with AIH complicated by EF. He was admitted to our hospital with acute hepatic injury and...

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Autores principales: Asada, Shohei, Douhara, Akitoshi, Murata, Koji, Yanase, Koji, Tsutsumi, Masahiro, Yoshiji, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443560/
https://www.ncbi.nlm.nih.gov/pubmed/30333401
http://dx.doi.org/10.2169/internalmedicine.1299-18
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author Asada, Shohei
Douhara, Akitoshi
Murata, Koji
Yanase, Koji
Tsutsumi, Masahiro
Yoshiji, Hitoshi
author_facet Asada, Shohei
Douhara, Akitoshi
Murata, Koji
Yanase, Koji
Tsutsumi, Masahiro
Yoshiji, Hitoshi
author_sort Asada, Shohei
collection PubMed
description Both autoimmune hepatitis (AIH) and eosinophilic fasciitis (EF) are known to be complicated by other autoimmune diseases. However, AIH complicated by EF has never been reported. We experienced a 58-year-old man with AIH complicated by EF. He was admitted to our hospital with acute hepatic injury and edema of the legs in April 201X. The etiologies of these symptoms were histologically proven as AIH and EF. The administration of prednisolone (PSL) drastically improved his liver injury and edema of the legs. When we make a diagnosis of AIH, we should carefully evaluate the physical findings, including the appearance of the legs, in order to detect other coexisting autoimmune diseases.
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spelling pubmed-64435602019-04-02 A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis Asada, Shohei Douhara, Akitoshi Murata, Koji Yanase, Koji Tsutsumi, Masahiro Yoshiji, Hitoshi Intern Med Case Report Both autoimmune hepatitis (AIH) and eosinophilic fasciitis (EF) are known to be complicated by other autoimmune diseases. However, AIH complicated by EF has never been reported. We experienced a 58-year-old man with AIH complicated by EF. He was admitted to our hospital with acute hepatic injury and edema of the legs in April 201X. The etiologies of these symptoms were histologically proven as AIH and EF. The administration of prednisolone (PSL) drastically improved his liver injury and edema of the legs. When we make a diagnosis of AIH, we should carefully evaluate the physical findings, including the appearance of the legs, in order to detect other coexisting autoimmune diseases. The Japanese Society of Internal Medicine 2018-10-17 2019-03-01 /pmc/articles/PMC6443560/ /pubmed/30333401 http://dx.doi.org/10.2169/internalmedicine.1299-18 Text en Copyright © 2019 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Asada, Shohei
Douhara, Akitoshi
Murata, Koji
Yanase, Koji
Tsutsumi, Masahiro
Yoshiji, Hitoshi
A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis
title A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis
title_full A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis
title_fullStr A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis
title_full_unstemmed A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis
title_short A Histologically Proven Case of Autoimmune Hepatitis with Eosinophilic Fasciitis
title_sort histologically proven case of autoimmune hepatitis with eosinophilic fasciitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443560/
https://www.ncbi.nlm.nih.gov/pubmed/30333401
http://dx.doi.org/10.2169/internalmedicine.1299-18
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