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Congenital absence of pericardium: two cases and a comprehensive review of the literature

机译:先天性心包缺失:2例并文献复习

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摘要

Congenital absence of pericardium (CAP) is a rare condition, generally asymptomatic or paucisymptomatic, nevertheless sporadic cases complicated by sudden death are described.CAP can be diagnosed by CT and MRI. It is classified as total or partial, and partial defects are divided into left defects and right defects.Interestingly, several articles highlight the correlation between CAP and some anatomical lung abnormalities, such as presence of lung parenchyma between the main pulmonary artery and ascending aorta, lung parenchyma between the base of the heart and left hemidiaphragm, and lung parenchyma between the proximal ascending aorta and right pulmonary artery.
机译:先天性心包缺乏症(CAP)是一种罕见病,通常无症状或有小症状,但有零星病例并发猝死,可以通过CT和MRI诊断。它分为全部或部分,部分缺损分为左缺损和右缺损。有趣的是,有几篇文章强调了CAP与一些解剖学上的肺部异常之间的相关性,例如在主肺动脉和升主动脉之间存在肺实质,肺实质位于心脏底部与左半he之间,而肺实质位于近端升主动脉与右肺动脉之间。

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