先天性左心包部分缺失。

S Kostiainen, T J Maamies
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引用次数: 0

摘要

一位38岁的女性先天性左心包部分缺失。这种情况相当罕见,通常在胸内手术或尸检时偶然诊断出来。文献报道了11例手术矫正病例。本病例因短暂发作的胸痛、心悸和呼吸困难而入院。当她左侧躺下时,这些攻击就发生了,并迅速改变了姿势。胸片显示左心边界上方突出,心脏稍左移。左侧诊断性气胸证实了心包缺损的诊断。缺损经心包成形术修复。由于心脏脱出心包和猝死的危险,手术矫正部分左心包缺损是必要的。据报道,感染从胸膜腔扩散到心包和心脏也造成了死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital partial absence of the left pericardium.

A 38 year old woman with congenital partial absence of the left pericardium is presented. The condition is fairly rare, usually diagnosed incidentally during intrathoracic operations or at autopsy. Eleven operatively corrected cases are reported in the literature. The present case was admitted because of transient attacks of chest pain, palpitation and dyspnoea. These attacks were brought on when she lay on her left side and were promptly relieved by a change of position. The chest radiograph revealed a prominence of the superior aspect of the left heart border and a slight laevo-position of the heart. A diagnostic pneumothorax on the left side confirmed the diagnosis of a pericardial defect. The defect was repaired by pericardioplasty. Operative correction of a partial left pericardial defect is indicated because of the danger of luxation of the heart out of the pericardium and sudden death. This has been reported, as well as a death caused by spreading of infection from the pleural cavity into the pericardium and heart.

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