Symptomatic giant left atrial aneurysm in a child: a rare entity.

Images in paediatric cardiology Pub Date : 2010-01-01
N Awasthy, M Tomar, S Radhakrishnan, S Shrivastava, Ks Iyer
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引用次数: 0

Abstract

Isolated left atrial aneurysms are rare entities in clinical practice. Usually the condition is diagnosed in the second to fourth decades of life. The presence of such lesions in the pediatric age group is scantily described. We present a 2 year boy who presented with complaints of excessive irritability, respiratory distress and swelling of the feet. On examination, child was tachypnoeic with irregularly irregular rhythm. Echo showed a huge aneurysmal LA appendage with severe left ventricle dysfunction. The child underwent surgical resection for same. Findings were confirmed intraoperatively but he continued to have low cardiac output state after the surgery, with frequent arrhythmias and expired on day 7 of surgery. The case is reviewed and compared with the available English literature.

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儿童有症状的巨大左心房动脉瘤:罕见病例。
孤立性左心房动脉瘤在临床上是罕见的。这种情况通常在生命的第二到第四十年被诊断出来。这种病变在儿童年龄组的存在很少被描述。我们提出一个2岁的男孩谁提出申诉过度烦躁,呼吸窘迫和肿胀的脚。经检查,患儿呼吸急促,节律不规则。超声显示巨大的动脉瘤状左室附属物伴严重的左心室功能障碍。孩子接受了手术切除。术中发现得到证实,但术后患者仍处于低心输出量状态,心律失常频繁,于手术第7天死亡。本文回顾了本病例,并与现有的英文文献进行了比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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