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Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature

Abernethy malformation, also called as congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Although rare, it is increasingly being reported and is important to diagnose given the adverse clinical consequences in untreated patients. It has myriad...

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Autores principales: Azad, Sushil, Arya, Adhi, Sitaraman, Radhakrishnan, Garg, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716315/
https://www.ncbi.nlm.nih.gov/pubmed/31516281
http://dx.doi.org/10.4103/apc.APC_185_18
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author Azad, Sushil
Arya, Adhi
Sitaraman, Radhakrishnan
Garg, Amit
author_facet Azad, Sushil
Arya, Adhi
Sitaraman, Radhakrishnan
Garg, Amit
author_sort Azad, Sushil
collection PubMed
description Abernethy malformation, also called as congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Although rare, it is increasingly being reported and is important to diagnose given the adverse clinical consequences in untreated patients. It has myriad of clinical presentations, from being completely asymptomatic to causing hepatic carcinoma, hepatic encephalopathy, severe pulmonary hypertension, and diffuse pulmonary arteriovenous malformation. We describe our experience with five cases in a tertiary pediatric cardiac care center with Abernethy malformation, with review of literature and also discuss possible therapeutic implications.
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spelling pubmed-67163152019-09-12 Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature Azad, Sushil Arya, Adhi Sitaraman, Radhakrishnan Garg, Amit Ann Pediatr Cardiol Review Article Abernethy malformation, also called as congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Although rare, it is increasingly being reported and is important to diagnose given the adverse clinical consequences in untreated patients. It has myriad of clinical presentations, from being completely asymptomatic to causing hepatic carcinoma, hepatic encephalopathy, severe pulmonary hypertension, and diffuse pulmonary arteriovenous malformation. We describe our experience with five cases in a tertiary pediatric cardiac care center with Abernethy malformation, with review of literature and also discuss possible therapeutic implications. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6716315/ /pubmed/31516281 http://dx.doi.org/10.4103/apc.APC_185_18 Text en Copyright: © 2019 Annals of Pediatric Cardiology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Azad, Sushil
Arya, Adhi
Sitaraman, Radhakrishnan
Garg, Amit
Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
title Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
title_full Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
title_fullStr Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
title_full_unstemmed Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
title_short Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
title_sort abernethy malformation: our experience from a tertiary cardiac care center and review of literature
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716315/
https://www.ncbi.nlm.nih.gov/pubmed/31516281
http://dx.doi.org/10.4103/apc.APC_185_18
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