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

Autor:	Koorosh Vahidshahi, Hamidreza Poor Ali-Akbar, Mohammad Rad Godarzi, Ramin Baghai Tehrani, Mohammad Mahdavi
Rok vydání:	2013
Předmět:	Male medicine.medical_specialty Heart malformation Coronary Vessel Anomalies Cardiovascular Abnormalities Subclavian Artery Pulmonary Artery Coronary Angiography Asymptomatic Diagnosis Differential Internal medicine medicine.artery Humans Medicine Abnormalities Multiple Computed tomography angiography Heart Failure medicine.diagnostic_test business.industry Follow up studies Infant Aberrant right subclavian artery General Medicine medicine.disease Aneurysm Echocardiography Heart failure Right coronary artery Pediatrics Perinatology and Child Health Pulmonary artery Cardiology medicine.symptom Deglutition Disorders Tomography X-Ray Computed Cardiology and Cardiovascular Medicine business Vascular Surgical Procedures Follow-Up Studies
Zdroj:	Cardiology in the Young. 24:935-937
ISSN:	1467-1107 1047-9511
DOI:	10.1017/s1047951113001510
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::442f4e08cb5136fe5c63be9faf2338d7 https://doi.org/10.1017/s1047951113001510 Zobrazit plný text záznamu