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Infantile scimitar syndrome with unusual associations

Scimitar syndrome is a variant of partial anomalous pulmonary venous connection (PAPVC), in which all or part of the right lung is drained by right pulmonary veins that anomalously connect to the inferior vena cava (IVC). The affected lung and its associated airways are often hypoplastic. In additio...

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Autores principales: Al-Shamrani, Abullah, AlSadi, Reem S., Elhoury, Motea E., AlHarbi, Adel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556286/
https://www.ncbi.nlm.nih.gov/pubmed/28674724
http://dx.doi.org/10.15537/smj.2017.7.18365
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author Al-Shamrani, Abullah
AlSadi, Reem S.
Elhoury, Motea E.
AlHarbi, Adel S.
author_facet Al-Shamrani, Abullah
AlSadi, Reem S.
Elhoury, Motea E.
AlHarbi, Adel S.
author_sort Al-Shamrani, Abullah
collection PubMed
description Scimitar syndrome is a variant of partial anomalous pulmonary venous connection (PAPVC), in which all or part of the right lung is drained by right pulmonary veins that anomalously connect to the inferior vena cava (IVC). The affected lung and its associated airways are often hypoplastic. In addition, aortopulmonary collateral vessels may be involved on the affected side, causing sequestration of that side; such involvement is commonly associated with cardiac defects. We report a case of infantile scimitar syndrome that involved a typical association with the right lung, but with extremely unusual associations with congenital hydrocephalus and heart blockage. The presentation of this case and the role of different diagnostic approaches and management are discussed.
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spelling pubmed-55562862017-08-28 Infantile scimitar syndrome with unusual associations Al-Shamrani, Abullah AlSadi, Reem S. Elhoury, Motea E. AlHarbi, Adel S. Saudi Med J Case Report Scimitar syndrome is a variant of partial anomalous pulmonary venous connection (PAPVC), in which all or part of the right lung is drained by right pulmonary veins that anomalously connect to the inferior vena cava (IVC). The affected lung and its associated airways are often hypoplastic. In addition, aortopulmonary collateral vessels may be involved on the affected side, causing sequestration of that side; such involvement is commonly associated with cardiac defects. We report a case of infantile scimitar syndrome that involved a typical association with the right lung, but with extremely unusual associations with congenital hydrocephalus and heart blockage. The presentation of this case and the role of different diagnostic approaches and management are discussed. Saudi Medical Journal 2017-07 /pmc/articles/PMC5556286/ /pubmed/28674724 http://dx.doi.org/10.15537/smj.2017.7.18365 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al-Shamrani, Abullah
AlSadi, Reem S.
Elhoury, Motea E.
AlHarbi, Adel S.
Infantile scimitar syndrome with unusual associations
title Infantile scimitar syndrome with unusual associations
title_full Infantile scimitar syndrome with unusual associations
title_fullStr Infantile scimitar syndrome with unusual associations
title_full_unstemmed Infantile scimitar syndrome with unusual associations
title_short Infantile scimitar syndrome with unusual associations
title_sort infantile scimitar syndrome with unusual associations
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556286/
https://www.ncbi.nlm.nih.gov/pubmed/28674724
http://dx.doi.org/10.15537/smj.2017.7.18365
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