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Left Atrial Drainage of the Right Superior Vena Cava: A Case Report

An isolated right superior vena cava (RSVC) draining into the left atrium represents a very rare congenital malformation, especially in the absence of a partial anomalous pulmonary venous return. This condition leads to hypoxemia, cyanosis, and clubbing without any other signs of heart defects. We d...

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Autores principales: Moradian, Maryam, Mortezaeian, Hojjat, Baghaei, Ramin, Ghadrdoost, Behshid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, 2006- 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246439/
https://www.ncbi.nlm.nih.gov/pubmed/30483319
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author Moradian, Maryam
Mortezaeian, Hojjat
Baghaei, Ramin
Ghadrdoost, Behshid
author_facet Moradian, Maryam
Mortezaeian, Hojjat
Baghaei, Ramin
Ghadrdoost, Behshid
author_sort Moradian, Maryam
collection PubMed
description An isolated right superior vena cava (RSVC) draining into the left atrium represents a very rare congenital malformation, especially in the absence of a partial anomalous pulmonary venous return. This condition leads to hypoxemia, cyanosis, and clubbing without any other signs of heart defects. We describe an 8-year-old girl, who was referred to our hospital due to unexplained cyanosis. Segmental approach in transthoracic echocardiography showed left atrial drainage of the RSVC, which was subsequently confirmed by contrast echocardiography and angiography. Surgical repair via trans-section and anastomosis of the superior vena cava to the right atrium was performed to prevent the complications of right-to-left shunting and cyanosis. During a 4-year follow-up, the patient remained in very good clinical status and her serial echocardiography was normal except for very mild left atrial and left ventricular enlargement.
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spelling pubmed-62464392018-11-27 Left Atrial Drainage of the Right Superior Vena Cava: A Case Report Moradian, Maryam Mortezaeian, Hojjat Baghaei, Ramin Ghadrdoost, Behshid J Tehran Heart Cent Case Report An isolated right superior vena cava (RSVC) draining into the left atrium represents a very rare congenital malformation, especially in the absence of a partial anomalous pulmonary venous return. This condition leads to hypoxemia, cyanosis, and clubbing without any other signs of heart defects. We describe an 8-year-old girl, who was referred to our hospital due to unexplained cyanosis. Segmental approach in transthoracic echocardiography showed left atrial drainage of the RSVC, which was subsequently confirmed by contrast echocardiography and angiography. Surgical repair via trans-section and anastomosis of the superior vena cava to the right atrium was performed to prevent the complications of right-to-left shunting and cyanosis. During a 4-year follow-up, the patient remained in very good clinical status and her serial echocardiography was normal except for very mild left atrial and left ventricular enlargement. Tehran University of Medical Sciences, 2006- 2018-04 /pmc/articles/PMC6246439/ /pubmed/30483319 Text en Copyright © 2015 Tehran Heart Center, Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Moradian, Maryam
Mortezaeian, Hojjat
Baghaei, Ramin
Ghadrdoost, Behshid
Left Atrial Drainage of the Right Superior Vena Cava: A Case Report
title Left Atrial Drainage of the Right Superior Vena Cava: A Case Report
title_full Left Atrial Drainage of the Right Superior Vena Cava: A Case Report
title_fullStr Left Atrial Drainage of the Right Superior Vena Cava: A Case Report
title_full_unstemmed Left Atrial Drainage of the Right Superior Vena Cava: A Case Report
title_short Left Atrial Drainage of the Right Superior Vena Cava: A Case Report
title_sort left atrial drainage of the right superior vena cava: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246439/
https://www.ncbi.nlm.nih.gov/pubmed/30483319
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