D-transposition of the great arteries with right-sided pulmonary hypoplasia

Unilateral pulmonary agenesis or aplasia (UPA) in combination with congenital heart defects is rare and has not been reported in connection with transposition of the great arteries. This case demonstrated dextroposition of the fetal heart, and subsequent scans could not clearly visualize the right p...

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Autores principales: Sterrett, Mary E, Chang, Eugene Y, Kumar, Neha, Willan, Keith B, Zyblewski, Sinai C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727913/
https://www.ncbi.nlm.nih.gov/pubmed/33311930
http://dx.doi.org/10.4103/apc.APC_183_20
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author Sterrett, Mary E
Chang, Eugene Y
Kumar, Neha
Willan, Keith B
Zyblewski, Sinai C
author_facet Sterrett, Mary E
Chang, Eugene Y
Kumar, Neha
Willan, Keith B
Zyblewski, Sinai C
author_sort Sterrett, Mary E
collection PubMed
description Unilateral pulmonary agenesis or aplasia (UPA) in combination with congenital heart defects is rare and has not been reported in connection with transposition of the great arteries. This case demonstrated dextroposition of the fetal heart, and subsequent scans could not clearly visualize the right pulmonary artery. UPA should be considered in the workup and counseling for a family in the setting of fetal heart malposition, as there is a significant clinical impact.
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spelling pubmed-77279132020-12-11 D-transposition of the great arteries with right-sided pulmonary hypoplasia Sterrett, Mary E Chang, Eugene Y Kumar, Neha Willan, Keith B Zyblewski, Sinai C Ann Pediatr Cardiol Case Report Unilateral pulmonary agenesis or aplasia (UPA) in combination with congenital heart defects is rare and has not been reported in connection with transposition of the great arteries. This case demonstrated dextroposition of the fetal heart, and subsequent scans could not clearly visualize the right pulmonary artery. UPA should be considered in the workup and counseling for a family in the setting of fetal heart malposition, as there is a significant clinical impact. Wolters Kluwer - Medknow 2020 2020-09-23 /pmc/articles/PMC7727913/ /pubmed/33311930 http://dx.doi.org/10.4103/apc.APC_183_20 Text en Copyright: © 2020 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 Case Report
Sterrett, Mary E
Chang, Eugene Y
Kumar, Neha
Willan, Keith B
Zyblewski, Sinai C
D-transposition of the great arteries with right-sided pulmonary hypoplasia
title D-transposition of the great arteries with right-sided pulmonary hypoplasia
title_full D-transposition of the great arteries with right-sided pulmonary hypoplasia
title_fullStr D-transposition of the great arteries with right-sided pulmonary hypoplasia
title_full_unstemmed D-transposition of the great arteries with right-sided pulmonary hypoplasia
title_short D-transposition of the great arteries with right-sided pulmonary hypoplasia
title_sort d-transposition of the great arteries with right-sided pulmonary hypoplasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727913/
https://www.ncbi.nlm.nih.gov/pubmed/33311930
http://dx.doi.org/10.4103/apc.APC_183_20
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