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An Unusual Case of Biatrial Myxoma in a Young Female

Myxoma, a rare type of intracardiac tumor, forms a very small percentage of the cardiac cases. Reports of biatrial myxoma are rarer, with cases of single tumor reaching both atria being more common. Here, we present an unusual case of two independently growing atrial myxoma in a 29-year-old female....

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Detalles Bibliográficos
Autores principales: Vijan, Vikrant, Vupputuri, Anjith, Chandrasekharan Nair, Rajiv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735894/
https://www.ncbi.nlm.nih.gov/pubmed/26881142
http://dx.doi.org/10.1155/2016/3545480
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author Vijan, Vikrant
Vupputuri, Anjith
Chandrasekharan Nair, Rajiv
author_facet Vijan, Vikrant
Vupputuri, Anjith
Chandrasekharan Nair, Rajiv
author_sort Vijan, Vikrant
collection PubMed
description Myxoma, a rare type of intracardiac tumor, forms a very small percentage of the cardiac cases. Reports of biatrial myxoma are rarer, with cases of single tumor reaching both atria being more common. Here, we present an unusual case of two independently growing atrial myxoma in a 29-year-old female. We emphasize that early recognition of symptoms, confirmation of diagnosis by transesophageal echocardiography, and prompt surgical excision remain vital in the management of such patients. The patient in the present case was managed successfully with no evidences of recurrence at the last follow-up.
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spelling pubmed-47358942016-02-15 An Unusual Case of Biatrial Myxoma in a Young Female Vijan, Vikrant Vupputuri, Anjith Chandrasekharan Nair, Rajiv Case Rep Cardiol Case Report Myxoma, a rare type of intracardiac tumor, forms a very small percentage of the cardiac cases. Reports of biatrial myxoma are rarer, with cases of single tumor reaching both atria being more common. Here, we present an unusual case of two independently growing atrial myxoma in a 29-year-old female. We emphasize that early recognition of symptoms, confirmation of diagnosis by transesophageal echocardiography, and prompt surgical excision remain vital in the management of such patients. The patient in the present case was managed successfully with no evidences of recurrence at the last follow-up. Hindawi Publishing Corporation 2016 2016-01-03 /pmc/articles/PMC4735894/ /pubmed/26881142 http://dx.doi.org/10.1155/2016/3545480 Text en Copyright © 2016 Vikrant Vijan et al. https://creativecommons.org/licenses/by/4.0/ 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
Vijan, Vikrant
Vupputuri, Anjith
Chandrasekharan Nair, Rajiv
An Unusual Case of Biatrial Myxoma in a Young Female
title An Unusual Case of Biatrial Myxoma in a Young Female
title_full An Unusual Case of Biatrial Myxoma in a Young Female
title_fullStr An Unusual Case of Biatrial Myxoma in a Young Female
title_full_unstemmed An Unusual Case of Biatrial Myxoma in a Young Female
title_short An Unusual Case of Biatrial Myxoma in a Young Female
title_sort unusual case of biatrial myxoma in a young female
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735894/
https://www.ncbi.nlm.nih.gov/pubmed/26881142
http://dx.doi.org/10.1155/2016/3545480
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