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有症状的心肌桥:一种常见的冠状动脉变异可导致患有潜在心脏疾病的患儿出现严重心肌缺血。

Symptomatic myocardial bridging: a frequently occurring coronary variation can cause severe myocardial ischaemia in affected children with underlying cardiac conditions.

作者信息

Kiess Alexandra, Vollroth Marcel, Bakhtiary Farhad, Seki Hiroshi, Kostelka Martin, Djukic Milan, Daehnert Ingo, Wagner Robert

机构信息

1Department of Pediatric Cardiology and Congenital Heart Disease,Heart Center,University of Leipzig,Leipzig,Germany.

2Department of Cardiac Surgery,Heart Center,University of Leipzig,Leipzig,Germany.

出版信息

Cardiol Young. 2018 Jun;28(6):826-831. doi: 10.1017/S1047951118000409. Epub 2018 May 16.

Abstract

Myocardial bridging is a congenital coronary artery anomaly in which the coronary artery has a partly "tunnelled" intramyocardial course. This tunnelling leads to compression of the affected vessel segment during ventricular systole. It is considered to be a benign variation of the norm in about 25% of the population caused by an aberrancy of embryologic coronary development. The bridging is also thought to cause severe cardiac conditions in a few of those affected. The series of six young patients presented here is the largest series so far to report on symptomatic myocardial bridging in children with different underlying heart diseases. All patients recently presented to our centre with signs of myocardial ischaemia. They subsequently underwent coronary angiography, which revealed myocardial bridging of the ramus interventricularis anterior. In all patients, therapy with β blockers was started to reduce heart rate and myocardial contractility. β Blocker treatment was also given in order to prolong diastole and improve coronary artery blood flow. Two patients underwent surgical exposure of the involved coronary segment: a 2-year-old boy because of recurrent, severe myocardial ischaemia in combination with a reduction of general health, changes in ST-segments, and the presence of a dilative cardiomyopathy; and a 13-year-old girl because of evidence of myocardial ischaemia during exercise testing after surviving sudden cardiac death. Surgery was successful and recovery was complete and uneventful. The presented series shows that myocardial bridging can be symptomatic and may require urgent treatment and even surgical intervention in early childhood in rare cases.

摘要

心肌桥是一种先天性冠状动脉异常,其中冠状动脉有部分走行于心肌内,呈“隧道”样。这种隧道样结构导致心室收缩期时受累血管段受压。在约25%的人群中,它被认为是一种正常的良性变异,由胚胎期冠状动脉发育异常引起。也有少数患者被认为会因心肌桥而出现严重心脏疾病。本文介绍的这组6例年轻患者是目前关于不同基础心脏病患儿有症状性心肌桥的最大病例系列报道。所有患者近期因心肌缺血症状就诊于我们中心。随后他们接受了冠状动脉造影,结果显示前室间支存在心肌桥。所有患者均开始使用β受体阻滞剂治疗,以降低心率和心肌收缩力。给予β受体阻滞剂治疗也是为了延长舒张期并改善冠状动脉血流。两名患者接受了受累冠状动脉段的手术显露:一名2岁男孩,因反复出现严重心肌缺血,伴有全身健康状况下降、ST段改变以及扩张型心肌病;另一名13岁女孩,因在心脏性猝死存活后运动试验时有心肌缺血证据。手术成功,恢复完全且顺利。该病例系列表明,心肌桥可能有症状,在极少数情况下,可能需要在儿童早期进行紧急治疗甚至手术干预。

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