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新生儿右心房特发性增大掩盖左心房动脉瘤。

Idiopathic enlargement of the right atrium masking left atrial aneurysm in a neonate.

机构信息

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, Pediatric Heart Center, University of Giessen, Giessen, HE, Germany.

出版信息

Cardiol Young. 2023 Nov;33(11):2446-2448. doi: 10.1017/S104795112300255X. Epub 2023 Jul 26.

Abstract

An idiopathic enlargement of the right atrium is an extremely rare cardiac malformation. There are no established guidelines for the management of this disease, especially concerning medical versus surgical therapeutic approach and the timing for an operation. We report in this case about a neonate that first was treated conservatively until the age of 5 month and finally got an operative resection of the aneurysm. After surgery, unexpected complications occurred. A second aneurysm in the left atrium was demasked. Furthermore, a progressive dilatation of both atrial chambers after resection required regular follow-up and ongoing evaluation of treatment.

摘要

右心房特发性扩张是一种极其罕见的心脏畸形。目前尚无关于这种疾病的治疗指南,特别是关于药物治疗与手术治疗方法以及手术时机的选择。我们在此报告一例新生儿病例,其首先接受了保守治疗,直到 5 个月大,最终接受了手术切除动脉瘤。手术后,出现了意外的并发症。左心房出现第二个动脉瘤。此外,切除后两个心房腔的渐进性扩张需要定期随访和持续评估治疗效果。

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