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Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation
Congenital sternal cleft is a rare abnormality resulting from fusion failure of sternum. It occurs in isolation or along with defects of abdominal wall, diaphragm, pericardium, and heart. Early surgical correction is required to protect the underlying structures for risk of cardiac compression. Here...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697142/ https://www.ncbi.nlm.nih.gov/pubmed/23841006 http://dx.doi.org/10.1155/2013/192478 |
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author | Saha, Anindya Kumar Sardar, Syamal Kumar Sur, Amitava |
author_facet | Saha, Anindya Kumar Sardar, Syamal Kumar Sur, Amitava |
author_sort | Saha, Anindya Kumar |
collection | PubMed |
description | Congenital sternal cleft is a rare abnormality resulting from fusion failure of sternum. It occurs in isolation or along with defects of abdominal wall, diaphragm, pericardium, and heart. Early surgical correction is required to protect the underlying structures for risk of cardiac compression. Here we report a case of 20-day female child presenting with congenital sternal cleft associated with multiple congenital heart disease and left-sided superior vena cava. She was operated by the cardiothoracic surgical team successfully and is doing well on followup. We discuss this rare case, imaging studies, and surgical strategy. |
format | Online Article Text |
id | pubmed-3697142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36971422013-07-09 Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation Saha, Anindya Kumar Sardar, Syamal Kumar Sur, Amitava Case Rep Pediatr Case Report Congenital sternal cleft is a rare abnormality resulting from fusion failure of sternum. It occurs in isolation or along with defects of abdominal wall, diaphragm, pericardium, and heart. Early surgical correction is required to protect the underlying structures for risk of cardiac compression. Here we report a case of 20-day female child presenting with congenital sternal cleft associated with multiple congenital heart disease and left-sided superior vena cava. She was operated by the cardiothoracic surgical team successfully and is doing well on followup. We discuss this rare case, imaging studies, and surgical strategy. Hindawi Publishing Corporation 2013 2013-06-13 /pmc/articles/PMC3697142/ /pubmed/23841006 http://dx.doi.org/10.1155/2013/192478 Text en Copyright © 2013 Anindya Kumar Saha et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Saha, Anindya Kumar Sardar, Syamal Kumar Sur, Amitava Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation |
title | Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation |
title_full | Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation |
title_fullStr | Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation |
title_full_unstemmed | Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation |
title_short | Congenital Sternal Cleft along with Persistent Left-Sided Superior Vena Cava: A Rare Presentation |
title_sort | congenital sternal cleft along with persistent left-sided superior vena cava: a rare presentation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697142/ https://www.ncbi.nlm.nih.gov/pubmed/23841006 http://dx.doi.org/10.1155/2013/192478 |
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