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Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia

Abernethy malformation is an extrahepatic congenital portosystemic shunt characterized by the diversion of the portal blood away from the liver through a shunt that drains directly into the inferior vena cava. We present a case of a male child with Abernethy malformation, which was initially diagnos...

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Autores principales: Agarwal, Rohit, Prasad, Durga, Chauhan, Gaurav, Verma, Abhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905039/
https://www.ncbi.nlm.nih.gov/pubmed/36779160
http://dx.doi.org/10.7759/cureus.33519
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author Agarwal, Rohit
Prasad, Durga
Chauhan, Gaurav
Verma, Abhai
author_facet Agarwal, Rohit
Prasad, Durga
Chauhan, Gaurav
Verma, Abhai
author_sort Agarwal, Rohit
collection PubMed
description Abernethy malformation is an extrahepatic congenital portosystemic shunt characterized by the diversion of the portal blood away from the liver through a shunt that drains directly into the inferior vena cava. We present a case of a male child with Abernethy malformation, which was initially diagnosed as cyanotic heart disease due to pulmonary arteriovenous malformation. However, after proper clinical evaluation and investigations, the diagnosis of Abernethy malformation was established. Thereafter, the patient was successfully treated with endovascular embolization. At one year follow-up, marked relief in exertional dyspnea and improvement in physical growth was achieved with no observable complications.
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spelling pubmed-99050392023-02-09 Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia Agarwal, Rohit Prasad, Durga Chauhan, Gaurav Verma, Abhai Cureus Cardiac/Thoracic/Vascular Surgery Abernethy malformation is an extrahepatic congenital portosystemic shunt characterized by the diversion of the portal blood away from the liver through a shunt that drains directly into the inferior vena cava. We present a case of a male child with Abernethy malformation, which was initially diagnosed as cyanotic heart disease due to pulmonary arteriovenous malformation. However, after proper clinical evaluation and investigations, the diagnosis of Abernethy malformation was established. Thereafter, the patient was successfully treated with endovascular embolization. At one year follow-up, marked relief in exertional dyspnea and improvement in physical growth was achieved with no observable complications. Cureus 2023-01-08 /pmc/articles/PMC9905039/ /pubmed/36779160 http://dx.doi.org/10.7759/cureus.33519 Text en Copyright © 2023, Agarwal et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Cardiac/Thoracic/Vascular Surgery
Agarwal, Rohit
Prasad, Durga
Chauhan, Gaurav
Verma, Abhai
Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia
title Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia
title_full Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia
title_fullStr Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia
title_full_unstemmed Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia
title_short Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia
title_sort abernethy malformation masquerading as congenital heart disease: a boy with cyanosis, clubbing, and hypoxia
topic Cardiac/Thoracic/Vascular Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905039/
https://www.ncbi.nlm.nih.gov/pubmed/36779160
http://dx.doi.org/10.7759/cureus.33519
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