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Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia
We describe the rare instance of concomitant biliary atresia and alpha-1-antitrypsin deficiency and the first documented successful portoenterostomy in this scenario. The potential for dual pathology must be recognized and underscores that prompt diagnosis of biliary atresia, despite concomitant alp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727568/ https://www.ncbi.nlm.nih.gov/pubmed/29318077 http://dx.doi.org/10.1155/2017/9348461 |
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author | Wang, Andrew W. Newton, Kimberly Kling, Karen |
author_facet | Wang, Andrew W. Newton, Kimberly Kling, Karen |
author_sort | Wang, Andrew W. |
collection | PubMed |
description | We describe the rare instance of concomitant biliary atresia and alpha-1-antitrypsin deficiency and the first documented successful portoenterostomy in this scenario. The potential for dual pathology must be recognized and underscores that prompt diagnosis of biliary atresia, despite concomitant alpha-1-antitrypsin deficiency, is essential to afford potential longstanding native liver function. |
format | Online Article Text |
id | pubmed-5727568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-57275682018-01-09 Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia Wang, Andrew W. Newton, Kimberly Kling, Karen Case Rep Surg Case Report We describe the rare instance of concomitant biliary atresia and alpha-1-antitrypsin deficiency and the first documented successful portoenterostomy in this scenario. The potential for dual pathology must be recognized and underscores that prompt diagnosis of biliary atresia, despite concomitant alpha-1-antitrypsin deficiency, is essential to afford potential longstanding native liver function. Hindawi 2017 2017-11-29 /pmc/articles/PMC5727568/ /pubmed/29318077 http://dx.doi.org/10.1155/2017/9348461 Text en Copyright © 2017 Andrew W. Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Wang, Andrew W. Newton, Kimberly Kling, Karen Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia |
title | Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia |
title_full | Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia |
title_fullStr | Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia |
title_full_unstemmed | Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia |
title_short | Successful Outcome and Biliary Drainage in an Infant with Concurrent Alpha-1-Antitrypsin Deficiency and Biliary Atresia |
title_sort | successful outcome and biliary drainage in an infant with concurrent alpha-1-antitrypsin deficiency and biliary atresia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727568/ https://www.ncbi.nlm.nih.gov/pubmed/29318077 http://dx.doi.org/10.1155/2017/9348461 |
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