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Congenital Aneurysm of the Right Atrium: Two Cases Report

Congenital aneurysm or enlargement of the right atrium is a rare condition. Two children operated on at the age of 14 months and 11 years old for congenital aneurysm of the right atrium are reported. Both presented cardiomegaly and symptoms of paroxysmal supraventricular tachycardia. Diagnosis was e...

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Autores principales: Melo, Halyna, Moraes Neto, Fernando, Lapa, Cleusa, Moraes, Carlos R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cirurgia Cardiovascular 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385824/
https://www.ncbi.nlm.nih.gov/pubmed/30810683
http://dx.doi.org/10.21470/1678-9741-2018-0047
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author Melo, Halyna
Moraes Neto, Fernando
Lapa, Cleusa
Moraes, Carlos R.
author_facet Melo, Halyna
Moraes Neto, Fernando
Lapa, Cleusa
Moraes, Carlos R.
author_sort Melo, Halyna
collection PubMed
description Congenital aneurysm or enlargement of the right atrium is a rare condition. Two children operated on at the age of 14 months and 11 years old for congenital aneurysm of the right atrium are reported. Both presented cardiomegaly and symptoms of paroxysmal supraventricular tachycardia. Diagnosis was established by echocardiography. Surgical resection was successful. Both patients are free of symptoms and their chest X-ray and echocardiogram are normal. The first patient is now in her 17(th) postoperative year. The patients' evolution suggests that the surgery is a curative procedure.
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spelling pubmed-63858242019-02-27 Congenital Aneurysm of the Right Atrium: Two Cases Report Melo, Halyna Moraes Neto, Fernando Lapa, Cleusa Moraes, Carlos R. Braz J Cardiovasc Surg Case Report Congenital aneurysm or enlargement of the right atrium is a rare condition. Two children operated on at the age of 14 months and 11 years old for congenital aneurysm of the right atrium are reported. Both presented cardiomegaly and symptoms of paroxysmal supraventricular tachycardia. Diagnosis was established by echocardiography. Surgical resection was successful. Both patients are free of symptoms and their chest X-ray and echocardiogram are normal. The first patient is now in her 17(th) postoperative year. The patients' evolution suggests that the surgery is a curative procedure. Sociedade Brasileira de Cirurgia Cardiovascular 2019 /pmc/articles/PMC6385824/ /pubmed/30810683 http://dx.doi.org/10.21470/1678-9741-2018-0047 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of 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
Melo, Halyna
Moraes Neto, Fernando
Lapa, Cleusa
Moraes, Carlos R.
Congenital Aneurysm of the Right Atrium: Two Cases Report
title Congenital Aneurysm of the Right Atrium: Two Cases Report
title_full Congenital Aneurysm of the Right Atrium: Two Cases Report
title_fullStr Congenital Aneurysm of the Right Atrium: Two Cases Report
title_full_unstemmed Congenital Aneurysm of the Right Atrium: Two Cases Report
title_short Congenital Aneurysm of the Right Atrium: Two Cases Report
title_sort congenital aneurysm of the right atrium: two cases report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385824/
https://www.ncbi.nlm.nih.gov/pubmed/30810683
http://dx.doi.org/10.21470/1678-9741-2018-0047
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