https://doi.org/10.4081/monaldi.2022.2246
Anomalous left coronary artery from pulmonary artery (ALCAPA) as a silent cause of mitral regurgitation in children
Submitted: February 22, 2022
Accepted: May 19, 2022
Published: June 23, 2022
Accepted: May 19, 2022
Abstract Views: 889
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Anomalous left coronary artery from pulmonary artery (ALCAPA), also known as Bland-White-Garland syndrome, is a rare cardiac disease. This condition may present with complications such as myocardial infarction, left ventricular dilatation, mitral regurgitation, and left heart failure in children. We report a case of a four-year-old boy who presented with shortness of breath, palpitations, and recurrent upper respiratory tract infections. He was diagnosed with mitral regurgitation. During the surgery, left coronary artery (LCA) was not present in its anatomical position and ALCAPA was identified. One should keep in mind the possibility of ALCAPA in presentation of mitral regurgitation in children despite not being reported in echocardiography.
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How to Cite
Ashraf, Naela, Suha Zubairi, Mehnaz Atiq, Farheen Ahmed, and Muneer Amanullah. 2022. “Anomalous Left Coronary Artery from Pulmonary Artery (ALCAPA) As a Silent Cause of Mitral Regurgitation in Children”. Monaldi Archives for Chest Disease 93 (1). https://doi.org/10.4081/monaldi.2022.2246.
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