A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome

Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary wi...

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Autores principales: Cui, Mingyue, Xia, Binfeng, Wang, Heru, Liu, Haihui, Yin, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829515/
https://www.ncbi.nlm.nih.gov/pubmed/33472471
http://dx.doi.org/10.1177/0300060520984656
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author Cui, Mingyue
Xia, Binfeng
Wang, Heru
Liu, Haihui
Yin, Xia
author_facet Cui, Mingyue
Xia, Binfeng
Wang, Heru
Liu, Haihui
Yin, Xia
author_sort Cui, Mingyue
collection PubMed
description Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta, with Eisenmenger syndrome and without surgery.
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spelling pubmed-78295152021-02-05 A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome Cui, Mingyue Xia, Binfeng Wang, Heru Liu, Haihui Yin, Xia J Int Med Res Case Report Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta, with Eisenmenger syndrome and without surgery. SAGE Publications 2021-01-20 /pmc/articles/PMC7829515/ /pubmed/33472471 http://dx.doi.org/10.1177/0300060520984656 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Cui, Mingyue
Xia, Binfeng
Wang, Heru
Liu, Haihui
Yin, Xia
A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome
title A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome
title_full A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome
title_fullStr A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome
title_full_unstemmed A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome
title_short A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome
title_sort rare case of adult aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta leading to eisenmenger syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829515/
https://www.ncbi.nlm.nih.gov/pubmed/33472471
http://dx.doi.org/10.1177/0300060520984656
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