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大动脉转位中的主动脉-右心室通道

Aorto-Right Ventricular Tunnel in Transposition of the Great Arteries.

作者信息

Corno Antonio F, Durairaj Saravanan, Anderson Robert H

机构信息

Cardiovascular Research Center, University of Leicester, Leicester, United Kingdom.

East Midlands Congenital Heart Center, University Hospitals of Leicester, Glenfield Hospital, Leicester, United Kingdom.

出版信息

Front Pediatr. 2018 Feb 21;6:30. doi: 10.3389/fped.2018.00030. eCollection 2018.

Abstract

Aorto-ventricular tunnel is an extremely rare congenital heart defect, consisting of failure of attachment of an aortic leaflet along the semilunar hinge. In all published reports the leaflet involved was either the right coronary leaflet, most frequently, or the left coronary leaflet, in most of the cases opening toward the left ventricle, with only one-eighth of the reported cases communicating with the right ventricle. Treatment of the aorto-ventricular tunnel has been anecdotally reported by interventional closure with a device and more frequently with surgical approach, either as an isolated malformation or as associated lesions. To the best of our knowledge, the presence of an aorto-ventricular tunnel of the non-adjacent aortic leaflet in transposition of the great arteries has never been reported. We have observed an aorto-ventricular tunnel involving the non-adjacent leaflet of the aortic root, which after arterial switch became the pulmonary root. The patient presented 18 years after the arterial switch with progressive dilatation of the right ventricle due to severe degree of pulmonary valve regurgitation, confirmed by echocardiography and cardiac MRI. Indication for surgery was given with the plan for a pulmonary valve implantation. Because of the intra-operative finding of disconnection of the anterior leaflet of the pulmonary valve (former aortic valve) along the semilunar hinge, the surgical plan was modified and the anterior leaflet was attached to the valve annulus, with subsequent plasty in correspondence with the right and left commissurae to reduce the size of the dilated annulus to normal diameter. The post-operative course was uneventful, with extubation after few hours and discharge 4 days after surgery, with echocardiography showing trivial degree of pulmonary valve regurgitation. The patient remains in good conditions 6 months after surgery.

摘要

主-室通道是一种极其罕见的先天性心脏缺陷,由主动脉瓣叶沿半月瓣铰链附着失败所致。在所有已发表的报告中,受累的瓣叶最常见的是右冠状动脉瓣叶,或在大多数情况下是左冠状动脉瓣叶,多数开口朝向左心室,只有八分之一的报告病例与右心室相通。主-室通道的治疗方法有通过器械介入封堵的零星报道,更常见的是采用手术方法,可作为孤立畸形或合并其他病变进行治疗。据我们所知,大动脉转位时非相邻主动脉瓣叶的主-室通道从未有过报道。我们观察到一例涉及主动脉根部非相邻瓣叶的主-室通道,在动脉调转术后该根部成为肺动脉根部。该患者在动脉调转术后18年因严重肺动脉瓣反流导致右心室进行性扩张,经超声心动图和心脏磁共振成像证实。手术指征为计划植入肺动脉瓣。由于术中发现肺动脉瓣(原主动脉瓣)前叶沿半月瓣铰链分离,手术方案被修改,将前叶附着于瓣膜环,并对左右交界进行成形术,以将扩张的瓣环尺寸缩小至正常直径。术后过程顺利,术后数小时拔管,术后4天出院,超声心动图显示肺动脉瓣反流程度轻微。患者术后6个月情况良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97d3/5826325/ef6cba004f4f/fped-06-00030-g001.jpg

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