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[自发性气胸的一种罕见病因]

[A Rare Cause of a Spontaneous Pneumothorax].

作者信息

Lepiorz M, Großer C, Hofmann H-S, Pfeifer M

机构信息

Klinik für Pneumologie und konservative Intensivmedizin - Krankenhaus Barmherzige Brüder, Regensburg.

Klinik für Thoraxchirurgie - Krankenhaus Barmherzige Brüder, Regensburg.

出版信息

Pneumologie. 2017 Sep;71(9):590-593. doi: 10.1055/s-0043-112886. Epub 2017 Jul 28.

Abstract

A young patient presented himself to the emergency department with sudden-onset, breathing-dependent right-sided thoracic pain. The auscultation revealed diminished breath sounds on the right. The radiograph showed a pneumothorax which was immediately dealt with chest tube drainage. The CT scan of the thorax showed minuscule subpleural bullae. Video-assisted thoracoscopic surgery (VATS) was performed due to persistent fistulae formation through the drain. The subpleural, bullous and emphysematous changes were histologically confirmed. Investigations into the cause showed evidence of alpha-1-antitrypsin deficiency (AATD). The patient is a Pi MZ type. Few cases of spontaneous pneumothorax as the first manifestation of alpha-1-antitrypsin deficiency have been described. When diagnosing primary spontaneous pneumothorax, alpha-1-antitrypsin deficiency should be considered.

摘要

一名年轻患者因突发、与呼吸相关的右侧胸痛前往急诊科就诊。听诊发现右侧呼吸音减弱。胸部X光片显示气胸,立即进行了胸腔闭式引流。胸部CT扫描显示有微小的胸膜下肺大疱。由于通过引流管持续形成瘘管,遂进行了电视辅助胸腔镜手术(VATS)。胸膜下、肺大疱和肺气肿改变经组织学证实。病因调查显示有α-1抗胰蛋白酶缺乏症(AATD)的证据。该患者为Pi MZ型。很少有将自发性气胸作为α-1抗胰蛋白酶缺乏症首发表现的病例报道。在诊断原发性自发性气胸时,应考虑α-1抗胰蛋白酶缺乏症。

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