Successful treatment of anomalous origin of the left coronary artery from the pulmonary artery in a 5-week-old male infant.

M Kamisago, S Ogawa, Y Hino, O Jimbo, Y Nagai, R Hayashi, T Seki, T Ohkubo, J Zhang, H Yamauchi, J Ninomiya, M Yamamoto
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引用次数: 1

Abstract

A 5-week-old male infant who was referred to our hospital because of tachypnea and poor feeding. An electrocardiogram showed a deep Q wave in lead aVL, negative T waves in leads I, II, III, aVF and V6 and a positive T wave in VL. Echocardiography revealed severely impaired left ventricular function. Aortography confirmed with a diagnosis of anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA). Takeuchi's procedure was performed and the patient maintained postoperatively on assisted circulation for 7 hours even though sternal closure delayed until 7 days post operatively. His left ventricular function showed and marked improvement gradually.

成功治疗1例5周大男婴左冠状动脉起源于肺动脉的异常。
一个5周大的男婴因呼吸急促和喂养不良被转介到我们医院。心电图示aVL导联深Q波,1、2、3、aVF、V6导联负T波,VL正T波。超声心动图显示左心室功能严重受损。主动脉造影证实左冠状动脉起源于肺动脉异常(ALCAPA)。采用Takeuchi手术,患者术后维持辅助循环7小时,尽管胸骨闭合延迟至术后7天。他的左心室功能逐渐有明显改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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