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Anomalous right coronary artery from the pulmonary artery (ARCAPA), and aberrant right subclavian artery in a 2-month infant with heart failure

Published online by Cambridge University Press:  29 October 2013

Mohammad Mahdavi ,
Koorosh Vahidshahi ,
Ramin Baghai Tehrani ,
Hamidreza Poor Ali-Akbar  and
Mohammad Rad Godarzi
Mohammad Mahdavi*
Affiliation:
Department of Pediatric Cardiology, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Koorosh Vahidshahi
Affiliation:
Department of Pediatric Cardiology, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Ramin Baghai Tehrani
Affiliation:
Department of Cardiovascular Surgery, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Hamidreza Poor Ali-Akbar
Affiliation:
Department of Radiology, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Mohammad Rad Godarzi
Affiliation:
Department of Pediatrics, Golestan University of Medical Science, Golestan, Iran
*
Correspondence to: Dr M. Mahdavi, Department of Peadiatric Cardiology, Rajaie Cardiovascular Medical and Research Center, Vali-asr Ave., Niyayesh Blvd., 199691-1151 Tehran, Iran. E-mail: [email protected]
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Abstract

Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare congenital heart anomaly. Most of the cases are asymptomatic during infancy and childhood. We report ARCAPA associated with aberrant right subclavian artery in a 2-month male infant presenting with heart failure. We used computed tomography angiography for confirming the diagnosis and also for post-operative follow-up.

Keywords

Anomalous origin of the right coronary artery from the pulmonary arteryinfantheart failure
Type
Brief Reports
Information
Cardiology in the Young , Volume 24 , Issue 5 , October 2014 , pp. 935 - 937
Copyright
Copyright © Cambridge University Press 2013 

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