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Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes

Anomalous origin of the right coronary artery from the left sinus of Valsalva and coursing between the aorta and pulmonary artery is a rare congenital abnormality representing less than 3% of the congenital coronary anomalies. Patients can present with myocardial ischemia, arrhythmias, or sudden car...

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Detalles Bibliográficos
Autores principales: Narayanan, Sunil Roy, Al Shamkhani, Warkaa, Rajappan, Anil Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867971/
https://www.ncbi.nlm.nih.gov/pubmed/27133342
http://dx.doi.org/10.1016/j.ihj.2016.01.016
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author Narayanan, Sunil Roy
Al Shamkhani, Warkaa
Rajappan, Anil Kumar
author_facet Narayanan, Sunil Roy
Al Shamkhani, Warkaa
Rajappan, Anil Kumar
author_sort Narayanan, Sunil Roy
collection PubMed
description Anomalous origin of the right coronary artery from the left sinus of Valsalva and coursing between the aorta and pulmonary artery is a rare congenital abnormality representing less than 3% of the congenital coronary anomalies. Patients can present with myocardial ischemia, arrhythmias, or sudden cardiac death (SCD). This diagnosis should be suspected in young patients without risk factors for coronary artery disease and the diagnosis can be confirmed easily by 64-slice MDCT angiography. Surgery is generally recommended in symptomatic patients whereas conservative management in asymptomatic patients. Incidence of SCD is rare after the age of 35 years and hence conservative treatment may be advised in asymptomatic patients over the age of 35 years.
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spelling pubmed-48679712017-03-01 Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes Narayanan, Sunil Roy Al Shamkhani, Warkaa Rajappan, Anil Kumar Indian Heart J Research Letter Anomalous origin of the right coronary artery from the left sinus of Valsalva and coursing between the aorta and pulmonary artery is a rare congenital abnormality representing less than 3% of the congenital coronary anomalies. Patients can present with myocardial ischemia, arrhythmias, or sudden cardiac death (SCD). This diagnosis should be suspected in young patients without risk factors for coronary artery disease and the diagnosis can be confirmed easily by 64-slice MDCT angiography. Surgery is generally recommended in symptomatic patients whereas conservative management in asymptomatic patients. Incidence of SCD is rare after the age of 35 years and hence conservative treatment may be advised in asymptomatic patients over the age of 35 years. Elsevier 2016 2016-02-06 /pmc/articles/PMC4867971/ /pubmed/27133342 http://dx.doi.org/10.1016/j.ihj.2016.01.016 Text en © 2015 Cardiological Society of India. Published by Elsevier B.V. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Letter
Narayanan, Sunil Roy
Al Shamkhani, Warkaa
Rajappan, Anil Kumar
Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes
title Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes
title_full Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes
title_fullStr Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes
title_full_unstemmed Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes
title_short Anomalous origin of RCA from left coronary sinus presenting as PSVT and recurrent acute coronary syndromes
title_sort anomalous origin of rca from left coronary sinus presenting as psvt and recurrent acute coronary syndromes
topic Research Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867971/
https://www.ncbi.nlm.nih.gov/pubmed/27133342
http://dx.doi.org/10.1016/j.ihj.2016.01.016
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