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首页> 外文期刊>Journal of cardiac surgery. >Congenital left main coronary artery to main pulmonary artery fistula with bicuspid aortic valve: A case report and review of literature
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Congenital left main coronary artery to main pulmonary artery fistula with bicuspid aortic valve: A case report and review of literature

机译:先天性左冠状动脉主干至肺动脉主干瘘伴二尖瓣主动脉瓣1例并文献复习

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摘要

Congenital coronary artery fistulas (CAFs) are uncommon abnormalities. A connection between the left main stem and main pulmonary artery is extremely rare. Congenital CAFs are frequently associated with another congenital heart disease. Associated anomalies include atrial septal defect, tetralogy of Fallot, patent ductus arteriosus, ventricular septal defect, and pulmonary atresia. Association of bicuspid aortic valve with CAF has not been reported in literature to date. We report on a 68-year-old man with congenital left main to pulmonary artery fistula associated with bicuspid aortic valve and moderate aortic stenoses, who underwent successful aortic valve replacement with ligation of CAF and also review the natural history, pathophysiology, and management of CAF.
机译:先天性冠状动脉瘘(CAF)是罕见的异常。左主干与肺主动脉之间的连接极少见。先天性CAF经常与另一种先天性心脏病有关。相关异常包括房间隔缺损,法洛四联症,动脉导管未闭,室间隔缺损和肺动脉闭锁。迄今为止,尚无文献报道双尖瓣主动脉瓣与CAF的关联。我们报道了一个68岁的男性,先天性左主干肺动脉瘘伴有二尖瓣主动脉瓣和中度主动脉狭窄,他们通过CAF结扎术成功地置换了主动脉瓣,并回顾了其自然病史,病理生理学和治疗CAF。

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