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Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature

Unilateral Absence of Pulmonary Artery (UAPA) is a rare congenital malformation that is usually associated with cardiac anomalies. When there is no congenital cardiac abnormality it is rarer still and is termed isolated unilateral absence of pulmonary artery (IUAPA) (4). IUAPA may remain undetected...

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Autores principales: Loo, Yi Jia, Thomas, Rajesh, Yagnik, Lokesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745554/
https://www.ncbi.nlm.nih.gov/pubmed/36523545
http://dx.doi.org/10.1002/rcr2.1073
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author Loo, Yi Jia
Thomas, Rajesh
Yagnik, Lokesh
author_facet Loo, Yi Jia
Thomas, Rajesh
Yagnik, Lokesh
author_sort Loo, Yi Jia
collection PubMed
description Unilateral Absence of Pulmonary Artery (UAPA) is a rare congenital malformation that is usually associated with cardiac anomalies. When there is no congenital cardiac abnormality it is rarer still and is termed isolated unilateral absence of pulmonary artery (IUAPA) (4). IUAPA may remain undetected until adulthood and frequently found incidentally on imaging for other indications. Symptoms are usually secondary to complications which include pulmonary hypertension, recurrent respiratory tract infections, bronchiectasis and haemoptysis. We report two cases with widely contrasting presentation and trajectories, leading to individualized management strategies.
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spelling pubmed-97455542022-12-14 Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature Loo, Yi Jia Thomas, Rajesh Yagnik, Lokesh Respirol Case Rep Case Reports Unilateral Absence of Pulmonary Artery (UAPA) is a rare congenital malformation that is usually associated with cardiac anomalies. When there is no congenital cardiac abnormality it is rarer still and is termed isolated unilateral absence of pulmonary artery (IUAPA) (4). IUAPA may remain undetected until adulthood and frequently found incidentally on imaging for other indications. Symptoms are usually secondary to complications which include pulmonary hypertension, recurrent respiratory tract infections, bronchiectasis and haemoptysis. We report two cases with widely contrasting presentation and trajectories, leading to individualized management strategies. John Wiley & Sons, Ltd 2022-12-13 /pmc/articles/PMC9745554/ /pubmed/36523545 http://dx.doi.org/10.1002/rcr2.1073 Text en © 2022 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Loo, Yi Jia
Thomas, Rajesh
Yagnik, Lokesh
Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature
title Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature
title_full Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature
title_fullStr Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature
title_full_unstemmed Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature
title_short Isolated unilateral absence of pulmonary artery (IUAPA) in adults: A case series and review of literature
title_sort isolated unilateral absence of pulmonary artery (iuapa) in adults: a case series and review of literature
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745554/
https://www.ncbi.nlm.nih.gov/pubmed/36523545
http://dx.doi.org/10.1002/rcr2.1073
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