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Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract
We present a case of a prematurely born 2‐month‐old girl with a double outlet right ventricle with pulmonary atresia and a left pulmonary artery coarctation arising after ductal closure. The case highlights the importance of knowledge and identification of such an anomaly in patients with congenital...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291456/ https://www.ncbi.nlm.nih.gov/pubmed/34637184 http://dx.doi.org/10.1111/jocs.16067 |
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author | van Vliet, Relin Kroft, Lucia J. M. Hazekamp, Mark G. Roest, Arno A. W. van der Palen, Roel L. F. |
author_facet | van Vliet, Relin Kroft, Lucia J. M. Hazekamp, Mark G. Roest, Arno A. W. van der Palen, Roel L. F. |
author_sort | van Vliet, Relin |
collection | PubMed |
description | We present a case of a prematurely born 2‐month‐old girl with a double outlet right ventricle with pulmonary atresia and a left pulmonary artery coarctation arising after ductal closure. The case highlights the importance of knowledge and identification of such an anomaly in patients with congenital heart malformations with severe pulmonary stenosis to atresia. |
format | Online Article Text |
id | pubmed-9291456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92914562022-07-20 Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract van Vliet, Relin Kroft, Lucia J. M. Hazekamp, Mark G. Roest, Arno A. W. van der Palen, Roel L. F. J Card Surg Case Image We present a case of a prematurely born 2‐month‐old girl with a double outlet right ventricle with pulmonary atresia and a left pulmonary artery coarctation arising after ductal closure. The case highlights the importance of knowledge and identification of such an anomaly in patients with congenital heart malformations with severe pulmonary stenosis to atresia. John Wiley and Sons Inc. 2021-10-12 2021-12 /pmc/articles/PMC9291456/ /pubmed/34637184 http://dx.doi.org/10.1111/jocs.16067 Text en © 2021 The Authors. Journal of Cardiac Surgery published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Image van Vliet, Relin Kroft, Lucia J. M. Hazekamp, Mark G. Roest, Arno A. W. van der Palen, Roel L. F. Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract |
title | Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract |
title_full | Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract |
title_fullStr | Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract |
title_full_unstemmed | Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract |
title_short | Pulmonary ductal coarctation: An entity associated with congenital heart defects involving the right ventricle outflow tract |
title_sort | pulmonary ductal coarctation: an entity associated with congenital heart defects involving the right ventricle outflow tract |
topic | Case Image |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291456/ https://www.ncbi.nlm.nih.gov/pubmed/34637184 http://dx.doi.org/10.1111/jocs.16067 |
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