Congenital lobar emphysema mis-interpreted as tension pneumothorax: a case report and literature review

被引:0
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作者
Ngam, Blessing N. [1 ]
Shu, Chinonso P. [1 ]
Tharion, John [4 ]
Brown, James A. [1 ,2 ]
Kamel, Armia S. F. [1 ]
Nwegbu, Chukwuemeka G. [3 ]
机构
[1] Mbingo Baptist Hosp, Pan African Acad Christian Surg PAACS, Bamenda, Cameroon
[2] Baptist Inst Hlth Sci BIHS, Surg Fac, Bamenda, Cameroon
[3] Mbingo Baptist Hosp, Gen Surg Pan African Acad Christian Surg, Bamenda, Cameroon
[4] Australian Natl Univ, Coll Hlth & Med, Canberra, Australia
关键词
adult CLE; case report; diagnosis; management; pneumothorax; DIAGNOSIS; PNEUMONECTOMY; CT;
D O I
10.1097/IO9.0000000000000011
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Introduction and importance: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.Case presentation: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.Discussion: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.Conclusion:Failure to recognize CLE or other cystic lung lesions can lead to harmful procedures.
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页码:24 / 28
页数:5
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