학술논문
Anomalous right coronary artery from the pulmonary artery in an infant with tetralogy of Fallot.
Document Type
Article
Source
Subject
*PULMONARY artery
*RARE diseases
*COMPUTED tomography
*PREOPERATIVE care
*CORONARY arteries
*TETRALOGY of Fallot
*ECHOCARDIOGRAPHY
*CHILDREN
CORONARY artery abnormalities
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Language
ISSN
0974-2069
Abstract
An anomalous right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital anomaly that does not have the typical presentation of the more common anomalous left coronary artery. We present an infant with tetralogy of Fallot with atypical findings on the preoperative echocardiogram. A cardiac computerized tomographic (CT) scan showed ARCAPA. This was confirmed intraoperatively and repaired successfully. Close attention to coronaries on echocardiography and a low threshold for additional imaging can successfully diagnose ARCAPA in the presence of additional congenital heart defects. [ABSTRACT FROM AUTHOR]