Chronic Hepatitis E is associated with cholangitis.


Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
10 2019
Historique:
received: 09 06 2017
revised: 21 12 2018
accepted: 06 02 2019
pubmed: 19 5 2019
medline: 22 9 2020
entrez: 19 5 2019
Statut: ppublish

Résumé

Sporadic hepatitis E is an emerging indigenous disease in Europe induced by genotype 3 of the virus. While the disease takes an acute self-limited course in immunocompetent individuals, under immunocompromised conditions chronic hepatitis E might develop. The histology of chronic hepatitis E has not been described in detail systematically. Liver biopsies from 19 immunosuppressed patients with chronic hepatitis E were collected: 17 were organ transplant recipients, one had a CD4-deficiency and one had received steroid therapy because of ulcerative colitis. Biopsies were processed with standard stains. Evaluation of histologic activity and fibrosis was performed according to Ishak. Additionally, immunohistochemistry with antibodies directed against open reading frame 2 and 3 of the virus was performed and liver biopsies were tested for hepatitis E virus RNA. Biochemical data showed an increase in alanine transaminase, aspartate transaminase, gamma-glutamyl transferase and total bilirubin. Histopathology displayed typical features of chronic hepatitis with mild to moderate activity. The number of polymorphonuclear leucocytes was considerably increased and all patients had a florid cholangitis that presented as a destructive form in five of them. Hepatocytes and bile duct epithelia stained positive for hepatitis E virus by immunohistochemistry. Chronic hepatitis E in immunocompromised individuals runs a similar course as hepatitis B and C and shows similar histopathology. However, the presence of destructive cholangitis in some cases accompanied by an increased number of polymorphonuclear leucocytes is markedly different. Immunohistochemically the virus is present in bile duct epithelia, seemingly the cause for cholangitis.

Sections du résumé

BACKGROUND AND AIMS
Sporadic hepatitis E is an emerging indigenous disease in Europe induced by genotype 3 of the virus. While the disease takes an acute self-limited course in immunocompetent individuals, under immunocompromised conditions chronic hepatitis E might develop. The histology of chronic hepatitis E has not been described in detail systematically.
METHODS
Liver biopsies from 19 immunosuppressed patients with chronic hepatitis E were collected: 17 were organ transplant recipients, one had a CD4-deficiency and one had received steroid therapy because of ulcerative colitis. Biopsies were processed with standard stains. Evaluation of histologic activity and fibrosis was performed according to Ishak. Additionally, immunohistochemistry with antibodies directed against open reading frame 2 and 3 of the virus was performed and liver biopsies were tested for hepatitis E virus RNA.
RESULTS
Biochemical data showed an increase in alanine transaminase, aspartate transaminase, gamma-glutamyl transferase and total bilirubin. Histopathology displayed typical features of chronic hepatitis with mild to moderate activity. The number of polymorphonuclear leucocytes was considerably increased and all patients had a florid cholangitis that presented as a destructive form in five of them. Hepatocytes and bile duct epithelia stained positive for hepatitis E virus by immunohistochemistry.
CONCLUSIONS
Chronic hepatitis E in immunocompromised individuals runs a similar course as hepatitis B and C and shows similar histopathology. However, the presence of destructive cholangitis in some cases accompanied by an increased number of polymorphonuclear leucocytes is markedly different. Immunohistochemically the virus is present in bile duct epithelia, seemingly the cause for cholangitis.

Identifiants

pubmed: 31102493
doi: 10.1111/liv.14137
pmc: PMC6790616
doi:

Substances chimiques

Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1876-1883

Informations de copyright

© 2019 The Authors. Liver International published by John Wiley & Sons Ltd.

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Auteurs

Andrea Beer (A)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Heidemarie Holzmann (H)

Department of Virology, Medical University of Vienna, Vienna, Austria.

Sven Pischke (S)

University Clinic Eppendorf, Hamburg, Germany.

Patrick Behrendt (P)

Department of Gastroenterology, Hepatology and Endocrinology, Medical School of Hanover, Hanover, Germany.

Fritz Wrba (F)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Jerome Schlue (J)

Institute for Pathology, Medical School of Hanover, Hanover, Germany.

Uta Drebber (U)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Barbara Neudert (B)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Emina Halilbasic (E)

Department of Gastroenterology, Medical University of Vienna, Vienna, Austria.

Hans Kreipe (H)

Institute for Pathology, Medical School of Hanover, Hanover, Germany.

Ansgar Lohse (A)

University Clinic Eppendorf, Hamburg, Germany.

Martina Sterneck (M)

University Clinic Eppendorf, Hamburg, Germany.

Heiner Wedemeyer (H)

Department of Gastroenterology, Hepatology and Endocrinology, Medical School of Hanover, Hanover, Germany.

Michael Manns (M)

Department of Gastroenterology, Hepatology and Endocrinology, Medical School of Hanover, Hanover, Germany.

Hans P Dienes (HP)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

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