Compression of an anomalous single coronary artery from pulmonary artery by banding

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Abstract

This report describes a case with double outlet right ventricle and doubly committed ventricular septal defect associated with congenital diaphragmatic hernia. The patient underwent pulmonary artery banding and clipping of patent ductus arteriosus after repair of the diaphragmatic hernia. At 6 months, cardiac catheterization revealed anomalous origin ofa single coronary artery from the pulmonary artery of the proximal banding. Although ischaemic symptoms had not been observed, the banding had resulted in compression of the coronary ostium. An emergency Rastelli procedure with Damus-Kaye-Stansel anastomosis was successfully performed. © The Author 2012. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

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Kawamura, A., Oshima, Y., Maruo, A., & Matsuhisa, H. (2012). Compression of an anomalous single coronary artery from pulmonary artery by banding. European Journal of Cardio-Thoracic Surgery, 41(4). https://doi.org/10.1093/ejcts/ezr269

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