新生儿巨大右心房附件动脉瘤成功治疗:一例罕见病例报告

IF 0.6 Q4 PEDIATRICS
Sudipta Bandyopadhyay , Swaminathan Vaidyanathan , C.S. Muthukumaran , Neville Solomon
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引用次数: 0

摘要

右心房附件动脉瘤是一种极为罕见的心脏异常。根据文献,到目前为止,在儿科人群中发现了10例病例。到目前为止,在新生儿时期进行手术修复的病例非常少。它可以是无症状的,也可能与心律失常或右心衰有关。这里我们提出一个新生儿的情况下,巨大的右心房附件动脉瘤,心律失常,并轻度呼吸窘迫。动脉瘤由经胸超声心动图诊断,并经心脏CT扫描证实。经体外循环手术切除。术后第2天拔管,第7天出院。由于其罕见的发生,诊断有时是困难的,它可能与Ebstein异常混淆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant right atrial appendage aneurysm successfully managed in a newborn: A rare case report

A right atrial appendage aneurysm is an extremely rare cardiac anomaly. According to the literature, so far, 10 cases have been detected in pediatric populations. A very small number of cases have so far undergone surgical repair in the newborn period. It can be asymptomatic or may be associated with arrhythmia or right heart failure. Here we are presenting a case of a newborn with a giant right atrial appendage aneurysm, arrhythmia, and mild respiratory distress. The aneurysm was diagnosed by transthoracic echocardiography and confirmed by a cardiac CT scan. It was resected surgically under cardiopulmonary bypass. Postoperatively, the baby was extubated on the 2nd postoperative day and discharged on the 7th postoperative day. Because of its rare occurrence, diagnosis is sometimes difficult, and it may be confused with the Ebstein anomaly.

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来源期刊
CiteScore
0.90
自引率
11.10%
发文量
69
审稿时长
75 days
期刊介绍: Progress in Pediatric Cardiology is an international journal of review presenting information and experienced opinion of importance in the understanding and management of cardiovascular diseases in children. Each issue is prepared by one or more Guest Editors and reviews a single subject, allowing for comprehensive presentations of complex, multifaceted or rapidly changing topics of clinical and investigative interest.
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