Volume 82, Issue 1 pp. 163-167
Pediatric and Congenital Heart Disease

Recurrent coronary artery thrombosis after anomalous right coronary artery re-implantation to the aorta

Seol Young Han MD

Seol Young Han MD

New York Methodist Hospital, New York

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John F. Heitner MD

John F. Heitner MD

New York Methodist Hospital, New York

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Sorin J. Brener MD

Corresponding Author

Sorin J. Brener MD

New York Methodist Hospital, New York

Correspondence to: Sorin J. Brener, MD, New York Methodist Hospital, Division of Cardiology, 506 Sixth Street, Brooklyn, NY 11215-9008. E-mail: [email protected]Search for more papers by this author
First published: 19 April 2012
Citations: 4

Conflict of interest: Nothing to report.

Abstract

Anomalous origin of the right coronary artery (RCA) from the pulmonary artery is a rare entity. The current recommendation is corrective operation even in asymptomatic patients when this cardiac malformation is found. We report a case of a 21-year-old male who initially presented with ST elevations. After surgical repair with re-implantation of the RCA to the aorta, he was found to have an acute thrombus in his left circumflex and several months later developed a thrombus in the proximal left anterior descending artery. We propose that the change from a hyperkinetic high flow state to a slow flow state in the setting of inadequate coronary flow reserve and endothelial function predisposed our patient to thrombus formation in the persistently dilated coronary arteries. It is expected that restoration of normal flow pattern in all coronary arteries will result in normalization of perfusion, decrease in feeding artery size, and return of endothelial function. Because this anomaly is rare, limited information exists on the effects of the procedure on myocardial perfusion. These findings raise the question of whether re-implantation of the anomalous artery is truly the superior approach. © 2013 Wiley Periodicals, Inc.

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