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Giant right atrium: a long-term complication of rheumatic heart disease

Giant right atrium (RA) is a rare entity often seen during childhood due to congenital anomalies. Limited literature has reported such finding in patients with rheumatic valvular heart disease. Here we present a case of a 68-year-old female with a history of rheumatic valve disease treated with a St...

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Detalles Bibliográficos
Autores principales: Abugroun, Ashraf, Taha, Mohamed, Daoud, Hussein, Ibrahim, Walid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588348/
https://www.ncbi.nlm.nih.gov/pubmed/33133628
http://dx.doi.org/10.1093/omcr/omaa011
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author Abugroun, Ashraf
Taha, Mohamed
Daoud, Hussein
Ibrahim, Walid
author_facet Abugroun, Ashraf
Taha, Mohamed
Daoud, Hussein
Ibrahim, Walid
author_sort Abugroun, Ashraf
collection PubMed
description Giant right atrium (RA) is a rare entity often seen during childhood due to congenital anomalies. Limited literature has reported such finding in patients with rheumatic valvular heart disease. Here we present a case of a 68-year-old female with a history of rheumatic valve disease treated with a Starr Edwards mechanical ball-in-cage mitral valve replacement and tricuspid valve annuloplasty ring procedures. The patient developed heart failure and had multiple hospital admissions over three decades for heart failure exacerbations mostly triggered by medication and dietary non-compliance. She eventually developed a giant RA that filled most of her thorax. This case demonstrates an extreme form of cardiac remodeling caused by long-term rheumatic valvular heart disease.
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spelling pubmed-75883482020-10-30 Giant right atrium: a long-term complication of rheumatic heart disease Abugroun, Ashraf Taha, Mohamed Daoud, Hussein Ibrahim, Walid Oxf Med Case Reports Case Report Giant right atrium (RA) is a rare entity often seen during childhood due to congenital anomalies. Limited literature has reported such finding in patients with rheumatic valvular heart disease. Here we present a case of a 68-year-old female with a history of rheumatic valve disease treated with a Starr Edwards mechanical ball-in-cage mitral valve replacement and tricuspid valve annuloplasty ring procedures. The patient developed heart failure and had multiple hospital admissions over three decades for heart failure exacerbations mostly triggered by medication and dietary non-compliance. She eventually developed a giant RA that filled most of her thorax. This case demonstrates an extreme form of cardiac remodeling caused by long-term rheumatic valvular heart disease. Oxford University Press 2020-02-28 /pmc/articles/PMC7588348/ /pubmed/33133628 http://dx.doi.org/10.1093/omcr/omaa011 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Abugroun, Ashraf
Taha, Mohamed
Daoud, Hussein
Ibrahim, Walid
Giant right atrium: a long-term complication of rheumatic heart disease
title Giant right atrium: a long-term complication of rheumatic heart disease
title_full Giant right atrium: a long-term complication of rheumatic heart disease
title_fullStr Giant right atrium: a long-term complication of rheumatic heart disease
title_full_unstemmed Giant right atrium: a long-term complication of rheumatic heart disease
title_short Giant right atrium: a long-term complication of rheumatic heart disease
title_sort giant right atrium: a long-term complication of rheumatic heart disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588348/
https://www.ncbi.nlm.nih.gov/pubmed/33133628
http://dx.doi.org/10.1093/omcr/omaa011
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