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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Saudi Medical Journal
2017
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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. |
format | Online Article Text |
id | pubmed-5556286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Saudi Medical Journal |
record_format | MEDLINE/PubMed |
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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