Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare congenital heart defect. Herein, we describe three cases of ARCAPA in an 8 months old, 18 months old, and 4 year old child. Two cases were incidentally diagnosed using a computed tomographic angiograph, a...

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Autores principales: Al-Dairy, Alwaleed, Rezaei, Yousef, Pouraliakbar, Hamidreza, Mahdavi, Mohammad, Bayati, Parvin, Gholampour-Dehaki, Maziar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Cardiology 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287178/
https://www.ncbi.nlm.nih.gov/pubmed/28154604
http://dx.doi.org/10.4070/kcj.2016.0174
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author Al-Dairy, Alwaleed
Rezaei, Yousef
Pouraliakbar, Hamidreza
Mahdavi, Mohammad
Bayati, Parvin
Gholampour-Dehaki, Maziar
author_facet Al-Dairy, Alwaleed
Rezaei, Yousef
Pouraliakbar, Hamidreza
Mahdavi, Mohammad
Bayati, Parvin
Gholampour-Dehaki, Maziar
author_sort Al-Dairy, Alwaleed
collection PubMed
description Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare congenital heart defect. Herein, we describe three cases of ARCAPA in an 8 months old, 18 months old, and 4 year old child. Two cases were incidentally diagnosed using a computed tomographic angiograph, and the other was incidentally diagnosed using a coronary angiograph. These cases underwent a reimplantation technique on diagnosis and resulting in positive clinical outcomes during the follow-up period which was a mean of 1.5 years.
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spelling pubmed-52871782017-02-02 Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery Al-Dairy, Alwaleed Rezaei, Yousef Pouraliakbar, Hamidreza Mahdavi, Mohammad Bayati, Parvin Gholampour-Dehaki, Maziar Korean Circ J Case Report Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare congenital heart defect. Herein, we describe three cases of ARCAPA in an 8 months old, 18 months old, and 4 year old child. Two cases were incidentally diagnosed using a computed tomographic angiograph, and the other was incidentally diagnosed using a coronary angiograph. These cases underwent a reimplantation technique on diagnosis and resulting in positive clinical outcomes during the follow-up period which was a mean of 1.5 years. The Korean Society of Cardiology 2017-01 2016-11-28 /pmc/articles/PMC5287178/ /pubmed/28154604 http://dx.doi.org/10.4070/kcj.2016.0174 Text en Copyright © 2017 The Korean Society of Cardiology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al-Dairy, Alwaleed
Rezaei, Yousef
Pouraliakbar, Hamidreza
Mahdavi, Mohammad
Bayati, Parvin
Gholampour-Dehaki, Maziar
Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
title Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
title_full Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
title_fullStr Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
title_full_unstemmed Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
title_short Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
title_sort surgical repair for anomalous origin of the right coronary artery from the pulmonary artery
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287178/
https://www.ncbi.nlm.nih.gov/pubmed/28154604
http://dx.doi.org/10.4070/kcj.2016.0174
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