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伴有完整间隔和发育不全右心室的共同动脉干:一种罕见的胚胎学实体。

Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity.

作者信息

Chikkagoudar Kalyanraddi, Gupta Palak, Koneti Nageswara Rao, Dash Tapan K, Doraiswamy Vinoth

机构信息

Department of Pediatric Cardiology, CARE Hospitals, Hyderabad, Telangana, India.

Department of Pediatric Cardiac Surgery, CARE Hospitals, Hyderabad, Telangana, India.

出版信息

Ann Pediatr Cardiol. 2020 Apr-Jun;13(2):157-159. doi: 10.4103/apc.APC_48_19. Epub 2020 Apr 13.

Abstract

Embryologically, the common arterial trunk (CAT) is due to the failure of septation by the major outflow cushions. This invariably leads to the presence of an associated large juxta-arterial ventricular septal defect. Overriding of the ventricular septum leads to its biventricular origin in more than 2/3 of cases. Uncommonly, CAT may be associated with an intact ventricular septum (IVS) and univentricular origin. We describe an infant with CAT, intact IVS, hypoplastic right ventricle, and Ebstein's anomaly of the tricuspid valve who presented to us and palliated successfully. The embryological mechanisms are discussed in this report.

摘要

从胚胎学角度来看,共同动脉干(CAT)是由于主要流出道垫的分隔失败所致。这必然会导致伴有一个大的动脉旁室间隔缺损。超过2/3的病例中,室间隔骑跨导致其双心室起源。罕见的是,CAT可能与完整的室间隔(IVS)和单心室起源相关。我们描述了一名患有CAT、IVS完整、右心室发育不全以及三尖瓣埃布斯坦畸形的婴儿,该婴儿前来就诊并成功接受了姑息治疗。本报告讨论了其胚胎学机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99f3/7331841/4feb0c231f36/APC-13-157-g001.jpg

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