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Total transcatheter correction of scimitar variant having dual pulmonary venous drainage
Scimitar syndrome is a clinical triad of anomalous pulmonary venous drainage, lung hypoplasia, and anomalous aortic blood supply to the lung segment. When there is dual pulmonary venous drainage both to inferior vena cava and left atrium, it is called scimitar variant. A young child presenting with...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727905/ https://www.ncbi.nlm.nih.gov/pubmed/33311925 http://dx.doi.org/10.4103/apc.APC_141_19 |
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author | Singh, Arvind Sahadev Sivakumar, Kothandam |
author_facet | Singh, Arvind Sahadev Sivakumar, Kothandam |
author_sort | Singh, Arvind Sahadev |
collection | PubMed |
description | Scimitar syndrome is a clinical triad of anomalous pulmonary venous drainage, lung hypoplasia, and anomalous aortic blood supply to the lung segment. When there is dual pulmonary venous drainage both to inferior vena cava and left atrium, it is called scimitar variant. A young child presenting with recurrent chest infections, dextroposition of the heart, and scimitar shadow on chest X-ray was identified to have scimitar variant after a detailed evaluation and managed successfully by catheter interventions. This report discusses the embryogenesis and angiographic findings of scimitar variants, indications for interventions, and issues in its management. |
format | Online Article Text |
id | pubmed-7727905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-77279052020-12-11 Total transcatheter correction of scimitar variant having dual pulmonary venous drainage Singh, Arvind Sahadev Sivakumar, Kothandam Ann Pediatr Cardiol Case Report Scimitar syndrome is a clinical triad of anomalous pulmonary venous drainage, lung hypoplasia, and anomalous aortic blood supply to the lung segment. When there is dual pulmonary venous drainage both to inferior vena cava and left atrium, it is called scimitar variant. A young child presenting with recurrent chest infections, dextroposition of the heart, and scimitar shadow on chest X-ray was identified to have scimitar variant after a detailed evaluation and managed successfully by catheter interventions. This report discusses the embryogenesis and angiographic findings of scimitar variants, indications for interventions, and issues in its management. Wolters Kluwer - Medknow 2020 2020-09-01 /pmc/articles/PMC7727905/ /pubmed/33311925 http://dx.doi.org/10.4103/apc.APC_141_19 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 Singh, Arvind Sahadev Sivakumar, Kothandam Total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
title | Total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
title_full | Total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
title_fullStr | Total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
title_full_unstemmed | Total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
title_short | Total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
title_sort | total transcatheter correction of scimitar variant having dual pulmonary venous drainage |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727905/ https://www.ncbi.nlm.nih.gov/pubmed/33311925 http://dx.doi.org/10.4103/apc.APC_141_19 |
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