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军人成年患者未诊断哮喘致自发性纵隔气肿。

Spontaneous Pneumomediastinum Secondary to Undiagnosed Asthma in Military Adult.

机构信息

Internal Medicine Residency Program, Wright-Patterson AFB Medical Center, Dayton, OH 45433, USA.

Pulmonary and Critical Care, Wright-Patterson AFB Medical Center, Dayton, OH 45433, USA.

出版信息

Mil Med. 2024 Jan 23;189(1-2):e433-e438. doi: 10.1093/milmed/usad263.

Abstract

Spontaneous pneumomediastinum (SPM) is a rare but described complication of exercise-induced bronchoconstriction (EIB), more commonly observed in children with asthma. We present a 23-year-old active duty military male and avid distance runner who developed progressive radiating retrosternal chest pain preceded by wheezing and coughing paroxysm. A chest computed tomography revealed extensive pneumomediastinum. SPM results from increased intrathoracic pressure with alveolar rupture and subsequent tracking of air between fascial planes. Like most cases of SPM, our patient remained hemodynamically stable and responded well to conservative therapies with complete resolution. After thorough evaluation, undiagnosed asthma was determined to be the inciting etiology. The patient is now well controlled and symptom free on a daily low-dose inhaled corticosteroid without SPM reoccurrence. In young adult patients presenting with SPM, EIB and asthma should be considered on the differential diagnosis as appropriate medical therapy will improve symptoms and reduce risk of reoccurrence.

摘要

自发性纵隔气肿(SPM)是运动性支气管收缩(EIB)的罕见但已描述的并发症,在哮喘儿童中更为常见。我们介绍了一位 23 岁的现役男性和热衷长跑的运动员,他在出现喘息和咳嗽发作之前出现进行性放射状胸骨后胸痛。胸部计算机断层扫描显示广泛的纵隔气肿。SPM 是由于胸腔内压力增加导致肺泡破裂,随后空气在筋膜平面之间跟踪所致。与大多数 SPM 病例一样,我们的患者血流动力学稳定,对保守治疗反应良好,完全缓解。经过彻底评估,确定未诊断的哮喘是引发病因。患者目前病情控制良好,每天使用低剂量吸入皮质类固醇,无症状,无 SPM 复发。在出现 SPM 的年轻成年患者中,应考虑 EIB 和哮喘作为鉴别诊断,因为适当的药物治疗将改善症状并降低复发风险。

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