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首页> 外文期刊>World Journal of Cardiovascular Diseases >Late surgical correction of anomalous left coronary artery from pulmonary trunk in children, using autogenous aortic and pulmonary endotheliazed tube
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Late surgical correction of anomalous left coronary artery from pulmonary trunk in children, using autogenous aortic and pulmonary endotheliazed tube

机译:自体主动脉和肺动脉内皮管对儿童肺动脉干左冠状动脉异常的晚期手术矫正

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Background: Direct re-implantation of an anomalous left coronary artery into the aorta is the preferred surgical option for creating a dual coronary arterial system in patients in whom the anomalous artery originated from the pulmonary trunk. This technique, however, is applicable only when the anomalous ar- tery arises from the left posterior pulmonary sinus. We report the successfully late follow-up of series of patients employing a new technique using combined autogenous aortic and pulmonary endotheliazed tube. Patients and Methods: We have treated 3 patients, aged 2 months, 6 months and 8 months respectively, who presented with anomalous origin of the left coronary artery from the left posterior pulmonary sinus and moderated mitral valve insufficiency by left ventricle dysfunction. We used a trapdoor like coronary artery elongation with autogenous aortic and pulmonary endotheliazed tube to connect the left coronary ostium to ascending aorta, avoiding the mitral valve intervention. Results: There was no early or late death. All patients are in functional class I, with good biventricular function and competent mitral valve at a median follow-up of 94 months, ranged from 108 to 132 months. Postoperative Computerized tomogramphy of aorta in our 1st patient showed good arterial flow, without any distortion. A local and distal stenosis of the left pulmonary artery was observed and submitted to stent treatment. Conclusions: The potential benefits of the trapdoor like and its modification technique are excellent operative exposure. The use of autogenous endothelized tube is a viable tissue capable of further growth, avoidance of injury to the aortic and pulmonary valvar apparatus or production of obstruction within the right ventricular outflow tract.
机译:背景:将异常左冠状动脉直接重新植入主动脉是在异常动脉起源于肺干的患者中创建双冠状动脉系统的首选手术选择。但是,该技术仅在左后肺窦出现异常血管时才适用。我们报告成功采用新技术使用自体主动脉和肺动脉内皮管相结合的一系列患者的成功后期随访。患者和方法:我们已收治了3例分别为2个月,6个月和8个月的患者,这些患者表现为左冠状动脉异常起源于左后肺窦,并因中度二尖瓣关闭不全而伴有左心室功能不全。我们使用自体主动脉和肺动脉内皮管之类的活板门如冠状动脉延长管将左冠状动脉口连接至升主动脉,避免了二尖瓣干预。结果:没有早期或晚期死亡。所有患者均属于I类功能,双心室功能良好,二尖瓣功能良好,中位随访时间为94个月,范围为108到132个月。术后第一例患者的主动脉电脑断层扫描显示动脉血流良好,没有任何扭曲。观察到左肺动脉的局部和远端狭窄并接受支架治疗。结论:活板门样及其改进技术的潜在益处是极好的手术暴露。自体内皮管的使用是一种可行的组织,能够进一步生长,避免对主动脉和肺动脉瓣膜装置的损伤或在右心室流出道内产生阻塞。

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