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Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report

BACKGROUND: Congenital extrahepatic portosystemic shunt, also known as Abernethy deformation, is a rare malformation caused by dysplasia in the portal vein system. There are few reports of liver transplantation as a treatment for Abernethy deformation, and our report is the first case in China. This...

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Autores principales: Xiang, Wen, Wang, Hao, Si, Zhong-Zhou, Chen, Guang-Shun, Wang, Guan-Wu, Li, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473130/
https://www.ncbi.nlm.nih.gov/pubmed/31024963
http://dx.doi.org/10.12998/wjcc.v7.i7.903
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author Xiang, Wen
Wang, Hao
Si, Zhong-Zhou
Chen, Guang-Shun
Wang, Guan-Wu
Li, Ting
author_facet Xiang, Wen
Wang, Hao
Si, Zhong-Zhou
Chen, Guang-Shun
Wang, Guan-Wu
Li, Ting
author_sort Xiang, Wen
collection PubMed
description BACKGROUND: Congenital extrahepatic portosystemic shunt, also known as Abernethy deformation, is a rare malformation caused by dysplasia in the portal vein system. There are few reports of liver transplantation as a treatment for Abernethy deformation, and our report is the first case in China. This is the second reported case with congenital extrahepatic portosystemic shunt combined with focal nodular hyperplasia and hepatopulmonary treated with liver transplantation. CASE SUMMARY: The patient was a 14-year-old girl, diagnosed preoperatively as type Ib Abernethy deformation, intrahepatic multiple space-occupying lesion, and hepatopulmonary syndrome. The patient recovered well after undergoing classic orthotopic liver transplantation. Liver function, pulmonary function, and portal vein computed tomography angiography imaging were reexamined 20 mo postoperatively, and no abnormality was observed. CONCLUSION: Liver transplantation is an effective treatment for type I Abernethy deformation combined with focal nodular hyperplasia and hepatopulmonary syndrome.
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spelling pubmed-64731302019-04-25 Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report Xiang, Wen Wang, Hao Si, Zhong-Zhou Chen, Guang-Shun Wang, Guan-Wu Li, Ting World J Clin Cases Case Report BACKGROUND: Congenital extrahepatic portosystemic shunt, also known as Abernethy deformation, is a rare malformation caused by dysplasia in the portal vein system. There are few reports of liver transplantation as a treatment for Abernethy deformation, and our report is the first case in China. This is the second reported case with congenital extrahepatic portosystemic shunt combined with focal nodular hyperplasia and hepatopulmonary treated with liver transplantation. CASE SUMMARY: The patient was a 14-year-old girl, diagnosed preoperatively as type Ib Abernethy deformation, intrahepatic multiple space-occupying lesion, and hepatopulmonary syndrome. The patient recovered well after undergoing classic orthotopic liver transplantation. Liver function, pulmonary function, and portal vein computed tomography angiography imaging were reexamined 20 mo postoperatively, and no abnormality was observed. CONCLUSION: Liver transplantation is an effective treatment for type I Abernethy deformation combined with focal nodular hyperplasia and hepatopulmonary syndrome. Baishideng Publishing Group Inc 2019-04-06 2019-04-06 /pmc/articles/PMC6473130/ /pubmed/31024963 http://dx.doi.org/10.12998/wjcc.v7.i7.903 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Xiang, Wen
Wang, Hao
Si, Zhong-Zhou
Chen, Guang-Shun
Wang, Guan-Wu
Li, Ting
Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report
title Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report
title_full Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report
title_fullStr Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report
title_full_unstemmed Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report
title_short Type I congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: A case report
title_sort type i congenital extrahepatic portosystemic shunt treated by orthotopic liver transplantation: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473130/
https://www.ncbi.nlm.nih.gov/pubmed/31024963
http://dx.doi.org/10.12998/wjcc.v7.i7.903
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