被误认为张力性气胸的先天性肺叶气肿:病例报告和文献综述

Pub Date : 2024-01-19 DOI:10.1097/io9.0000000000000011
B. N. Ngam, Chinonso P. Shu, John Tharion, James A. Brown, Armia S.F. Kamel, C. G. Nwegbu
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引用次数: 0

摘要

先天性肺大叶气肿(CLE)是一种罕见的肺发育异常,偶尔会在成年前一直没有症状。正确的诊断对其治疗至关重要。 作者报告了一个 29 岁的非吸烟男性病例。他曾被误诊为张力性气胸,后转诊至医院。他最初的症状是慢性咳嗽和进行性呼吸困难。他的胸片显示右肺野无肺标记,气管偏向左侧,被解释为张力性气胸。然而,插入胸管后,他的呼吸困难加重了。计算机断层扫描最初被解释为气胸,但结果显示与 CLE 一致。 成人 CLE 是一种非常罕见的病症。计算机断层扫描是首选的造影检查。尽管对特定患者进行观察等待是合理的,但肺叶切除术仍是标准的治疗方法,最好通过视频辅助胸腔手术进行。 如果未能识别 CLE 或其他肺囊性病变,可能会导致有害的手术。
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Congenital lobar emphysema mis-interpreted as tension pneumothorax: a case report and literature review
Congenital lobar emphysema (CLE) is a rare developmental lung anomaly that occasionally remains asymptomatic until adulthood. The right diagnosis is very crucial in its management. The authors report the case of a 29-year-old otherwise healthy, nonsmoker male. Referred after management of a presumptuous diagnosis of tension pneumothorax. His symptoms at initial presentation were a chronic cough and progressive exertional dyspnea. His chest radiography revealed absent lung markings in the right lung field with a trachea deviation to the left, interpreted as a tension pneumothorax. However, chest tube insertion worsened his dyspnea. A computed tomography scan, though initially interpreted as pneumothorax, showed findings consistent with CLE. Adult CLE is a very rare presentation. A computed tomography scan is the imaging of choice. Even though watchful waiting is reasonable in selected patients, lobectomy remains the standard of care, preferably via video-assisted thoracic surgery. Failure to recognize CLE or other cystic lung lesions can lead to harmful procedures.
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