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Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia

A 49-year-old woman presented with recurrent palpitations and presyncope. Monitoring revealed recurrent non-sustained ventricular tachycardia (VT) episodes. Cardiac catheterization showed the right coronary artery originating from the left coronary cusp. Cardiac computerized tomography revealed the...

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Detalles Bibliográficos
Autores principales: Hernandez, Ilsen E., Prakash, Atul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MediaSphere Medical 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193872/
https://www.ncbi.nlm.nih.gov/pubmed/37216087
http://dx.doi.org/10.19102/icrm.2023.14051
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author Hernandez, Ilsen E.
Prakash, Atul
author_facet Hernandez, Ilsen E.
Prakash, Atul
author_sort Hernandez, Ilsen E.
collection PubMed
description A 49-year-old woman presented with recurrent palpitations and presyncope. Monitoring revealed recurrent non-sustained ventricular tachycardia (VT) episodes. Cardiac catheterization showed the right coronary artery originating from the left coronary cusp. Cardiac computerized tomography revealed the course between the aorta and the pulmonary artery. Despite surgical correction, VT persisted. Genetic testing revealed a rare BCL2-associated athanogene 3 (BAG3) variant associated with dilated cardiomyopathy.
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spelling pubmed-101938722023-05-19 Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia Hernandez, Ilsen E. Prakash, Atul J Innov Card Rhythm Manag Case Report A 49-year-old woman presented with recurrent palpitations and presyncope. Monitoring revealed recurrent non-sustained ventricular tachycardia (VT) episodes. Cardiac catheterization showed the right coronary artery originating from the left coronary cusp. Cardiac computerized tomography revealed the course between the aorta and the pulmonary artery. Despite surgical correction, VT persisted. Genetic testing revealed a rare BCL2-associated athanogene 3 (BAG3) variant associated with dilated cardiomyopathy. MediaSphere Medical 2023-05-15 /pmc/articles/PMC10193872/ /pubmed/37216087 http://dx.doi.org/10.19102/icrm.2023.14051 Text en Copyright: © 2023 Innovations in Cardiac Rhythm Management https://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
Hernandez, Ilsen E.
Prakash, Atul
Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia
title Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia
title_full Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia
title_fullStr Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia
title_full_unstemmed Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia
title_short Coexisting BAG3 Variant and the Anomalous Origin of the Right Coronary Artery Presenting with Recurrent Ventricular Tachycardia
title_sort coexisting bag3 variant and the anomalous origin of the right coronary artery presenting with recurrent ventricular tachycardia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193872/
https://www.ncbi.nlm.nih.gov/pubmed/37216087
http://dx.doi.org/10.19102/icrm.2023.14051
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