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伪装成重度难治性哮喘的肺动脉高压

Pulmonary arterial hypertension masquerading as severe refractory asthma.

作者信息

Achouh L, Montani D, Garcia G, Jaïs X, Hamid A M, Mercier O, Simonneau G, Humbert M

机构信息

Université Paris-Sud 11, Centre National de Référence de L'Hypertension Artérielle Pulmonaire, Service de Pneumologie et Réanimation Respiratoire, Hôpital Antoine-Béclère, Clamart, France.

出版信息

Eur Respir J. 2008 Aug;32(2):513-6. doi: 10.1183/09031936.00005408.

Abstract

Once the diagnosis of pulmonary arterial hypertension is established, wheezing and chronic cough are rarely described during the course of the disease. The present study reports on two nonsmoking patients with severe pulmonary arterial hypertension, confirmed by right-heart catheterisation, who developed chronic cough, wheezing and irreversible obstructive lung disease masquerading as adult-onset severe refractory asthma. In both cases, extrinsic proximal airway obstruction by dilated pulmonary arteries was demonstrated by fibreoptic bronchoscopy and computed tomography of the chest. The present observations add dilatation of the central pulmonary arteries with compression of the mainstem bronchi to the list of masqueraders of asthma in patients with pulmonary arterial hypertension.

摘要

一旦确诊为肺动脉高压,在疾病过程中很少会出现喘息和慢性咳嗽。本研究报告了两名经右心导管检查确诊为重度肺动脉高压的非吸烟患者,他们出现了慢性咳嗽、喘息和伪装成成人起病的重度难治性哮喘的不可逆阻塞性肺疾病。在这两个病例中,纤维支气管镜检查和胸部计算机断层扫描均显示扩张的肺动脉导致外在性近端气道阻塞。本观察结果表明,在肺动脉高压患者中,中央肺动脉扩张伴主支气管受压是哮喘伪装者之一。

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