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Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta

The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have re...

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Detalles Bibliográficos
Autores principales: Zeng, Shi, Zhou, Qichang, Zhou, Jiawei, Peng, Qinghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502634/
https://www.ncbi.nlm.nih.gov/pubmed/26199806
http://dx.doi.org/10.1055/s-0035-1547331
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author Zeng, Shi
Zhou, Qichang
Zhou, Jiawei
Peng, Qinghai
author_facet Zeng, Shi
Zhou, Qichang
Zhou, Jiawei
Peng, Qinghai
author_sort Zeng, Shi
collection PubMed
description The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have reported fetal anomalous origin of PA from aorta with other malformation. We report a case of isolated distal anomalous origin of the right PA from the aorta that was diagnosed by fetal echocardiography at 25 weeks' of gestation. Tracing the course of PA branches is important to make diagnosis.
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spelling pubmed-45026342015-07-21 Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta Zeng, Shi Zhou, Qichang Zhou, Jiawei Peng, Qinghai AJP Rep Article The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have reported fetal anomalous origin of PA from aorta with other malformation. We report a case of isolated distal anomalous origin of the right PA from the aorta that was diagnosed by fetal echocardiography at 25 weeks' of gestation. Tracing the course of PA branches is important to make diagnosis. Thieme Medical Publishers 2015-03-04 2015-04 /pmc/articles/PMC4502634/ /pubmed/26199806 http://dx.doi.org/10.1055/s-0035-1547331 Text en © Thieme Medical Publishers
spellingShingle Article
Zeng, Shi
Zhou, Qichang
Zhou, Jiawei
Peng, Qinghai
Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
title Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
title_full Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
title_fullStr Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
title_full_unstemmed Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
title_short Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
title_sort fetal isolated anomalous origin of right pulmonary artery from aorta
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502634/
https://www.ncbi.nlm.nih.gov/pubmed/26199806
http://dx.doi.org/10.1055/s-0035-1547331
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