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Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report

Although it occurs worldwide, hepatitis E virus (HEV) infection in developed countries is generally foodborne. HEV infection is subclinical in most individuals. Although fulminant liver failure may occur, progression to chronic hepatitis is rare. This study describes a 41-year-old man with liver cir...

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Autores principales: Kurihara, Takeshi, Yoshizumi, Tomoharu, Itoh, Shinji, Harimoto, Norifumi, Harada, Noboru, Ikegami, Toru, Inagaki, Yuki, Oshiro, Yukio, Ohkohchi, Nobuhiro, Okamoto, Hiroaki, Maehara, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826363/
https://www.ncbi.nlm.nih.gov/pubmed/27059470
http://dx.doi.org/10.1186/s40792-016-0159-0
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author Kurihara, Takeshi
Yoshizumi, Tomoharu
Itoh, Shinji
Harimoto, Norifumi
Harada, Noboru
Ikegami, Toru
Inagaki, Yuki
Oshiro, Yukio
Ohkohchi, Nobuhiro
Okamoto, Hiroaki
Maehara, Yoshihiko
author_facet Kurihara, Takeshi
Yoshizumi, Tomoharu
Itoh, Shinji
Harimoto, Norifumi
Harada, Noboru
Ikegami, Toru
Inagaki, Yuki
Oshiro, Yukio
Ohkohchi, Nobuhiro
Okamoto, Hiroaki
Maehara, Yoshihiko
author_sort Kurihara, Takeshi
collection PubMed
description Although it occurs worldwide, hepatitis E virus (HEV) infection in developed countries is generally foodborne. HEV infection is subclinical in most individuals. Although fulminant liver failure may occur, progression to chronic hepatitis is rare. This study describes a 41-year-old man with liver cirrhosis caused by non-alcoholic steatohepatitis and hepatocellular carcinoma within the Milan criteria. His liver function was classified as Child-Pugh grade C. Living donor liver transplantation (LDLT) was performed, and he was discharged from the hospital on postoperative day (POD) 22. However, his alanine aminotransferase concentration began to increase on POD 60 and HEV infection was detected on POD 81. Retrospective assessments of stored blood samples showed that this patient became positive for HEV RNA on POD 3. The liver donor was negative for anti-HEV antibodies and HEV RNA. However, the platelet concentrate transfused into the liver recipient the day after LDLT was positive for HEV RNA. The patient remained positive for HEV infection for 10 months. Treatment with 800 mg/day ribavirin for 20 weeks reduced HEV RNA to an undetectable level. In conclusion, this report describes a patient infected with HEV through a blood transfusion after LDLT, who progressed to chronic hepatitis probably due to his immunosuppressed state and was treated well with ribavirin therapy.
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spelling pubmed-48263632016-04-20 Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report Kurihara, Takeshi Yoshizumi, Tomoharu Itoh, Shinji Harimoto, Norifumi Harada, Noboru Ikegami, Toru Inagaki, Yuki Oshiro, Yukio Ohkohchi, Nobuhiro Okamoto, Hiroaki Maehara, Yoshihiko Surg Case Rep Case Report Although it occurs worldwide, hepatitis E virus (HEV) infection in developed countries is generally foodborne. HEV infection is subclinical in most individuals. Although fulminant liver failure may occur, progression to chronic hepatitis is rare. This study describes a 41-year-old man with liver cirrhosis caused by non-alcoholic steatohepatitis and hepatocellular carcinoma within the Milan criteria. His liver function was classified as Child-Pugh grade C. Living donor liver transplantation (LDLT) was performed, and he was discharged from the hospital on postoperative day (POD) 22. However, his alanine aminotransferase concentration began to increase on POD 60 and HEV infection was detected on POD 81. Retrospective assessments of stored blood samples showed that this patient became positive for HEV RNA on POD 3. The liver donor was negative for anti-HEV antibodies and HEV RNA. However, the platelet concentrate transfused into the liver recipient the day after LDLT was positive for HEV RNA. The patient remained positive for HEV infection for 10 months. Treatment with 800 mg/day ribavirin for 20 weeks reduced HEV RNA to an undetectable level. In conclusion, this report describes a patient infected with HEV through a blood transfusion after LDLT, who progressed to chronic hepatitis probably due to his immunosuppressed state and was treated well with ribavirin therapy. Springer Berlin Heidelberg 2016-04-08 /pmc/articles/PMC4826363/ /pubmed/27059470 http://dx.doi.org/10.1186/s40792-016-0159-0 Text en © Kurihara et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Kurihara, Takeshi
Yoshizumi, Tomoharu
Itoh, Shinji
Harimoto, Norifumi
Harada, Noboru
Ikegami, Toru
Inagaki, Yuki
Oshiro, Yukio
Ohkohchi, Nobuhiro
Okamoto, Hiroaki
Maehara, Yoshihiko
Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report
title Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report
title_full Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report
title_fullStr Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report
title_full_unstemmed Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report
title_short Chronic hepatitis E virus infection after living donor liver transplantation via blood transfusion: a case report
title_sort chronic hepatitis e virus infection after living donor liver transplantation via blood transfusion: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826363/
https://www.ncbi.nlm.nih.gov/pubmed/27059470
http://dx.doi.org/10.1186/s40792-016-0159-0
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