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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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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. |
format | Online Article Text |
id | pubmed-6473130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
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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