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Partial anomalous pulmonary venous return: A case series with management approach
Partial anomalous pulmonary venous return (PAPVR) is a rare congenital anomaly that results in a left-to-right shunt. Based on the shunt fraction, PAPVR has a wide spectrum of presentations. If a significant left-to-right shunt is left unrepaired, pulmonary vascular remodeling can occur resulting in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456451/ https://www.ncbi.nlm.nih.gov/pubmed/31008046 http://dx.doi.org/10.1016/j.rmcr.2019.100833 |
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author | El-Kersh, Karim Homsy, Elie Daniels, Curt J. Smith, J. Shaun |
author_facet | El-Kersh, Karim Homsy, Elie Daniels, Curt J. Smith, J. Shaun |
author_sort | El-Kersh, Karim |
collection | PubMed |
description | Partial anomalous pulmonary venous return (PAPVR) is a rare congenital anomaly that results in a left-to-right shunt. Based on the shunt fraction, PAPVR has a wide spectrum of presentations. If a significant left-to-right shunt is left unrepaired, pulmonary vascular remodeling can occur resulting in the development of pulmonary arterial hypertension (PAH). Furthermore, if the condition is associated with an atrial septal defect (ASD), the patient can develop shunt reversal and Eisenmenger's syndrome in setting of severe PAH. Management plans include close observation, surgical repair, and treatment with pulmonary artery vasodilator therapies. Here, we present multiple cases of PAPVR to highlight the wide spectrum of presentations and the individualized treatment for each case. |
format | Online Article Text |
id | pubmed-6456451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-64564512019-04-19 Partial anomalous pulmonary venous return: A case series with management approach El-Kersh, Karim Homsy, Elie Daniels, Curt J. Smith, J. Shaun Respir Med Case Rep Article Partial anomalous pulmonary venous return (PAPVR) is a rare congenital anomaly that results in a left-to-right shunt. Based on the shunt fraction, PAPVR has a wide spectrum of presentations. If a significant left-to-right shunt is left unrepaired, pulmonary vascular remodeling can occur resulting in the development of pulmonary arterial hypertension (PAH). Furthermore, if the condition is associated with an atrial septal defect (ASD), the patient can develop shunt reversal and Eisenmenger's syndrome in setting of severe PAH. Management plans include close observation, surgical repair, and treatment with pulmonary artery vasodilator therapies. Here, we present multiple cases of PAPVR to highlight the wide spectrum of presentations and the individualized treatment for each case. Elsevier 2019-04-03 /pmc/articles/PMC6456451/ /pubmed/31008046 http://dx.doi.org/10.1016/j.rmcr.2019.100833 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article El-Kersh, Karim Homsy, Elie Daniels, Curt J. Smith, J. Shaun Partial anomalous pulmonary venous return: A case series with management approach |
title | Partial anomalous pulmonary venous return: A case series with management approach |
title_full | Partial anomalous pulmonary venous return: A case series with management approach |
title_fullStr | Partial anomalous pulmonary venous return: A case series with management approach |
title_full_unstemmed | Partial anomalous pulmonary venous return: A case series with management approach |
title_short | Partial anomalous pulmonary venous return: A case series with management approach |
title_sort | partial anomalous pulmonary venous return: a case series with management approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456451/ https://www.ncbi.nlm.nih.gov/pubmed/31008046 http://dx.doi.org/10.1016/j.rmcr.2019.100833 |
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