Vu Le Thuong, Duc Nguyen Minh, Tra My Thieu-Thi, Bang Luong Viet, My Le-Thi, Phuong Thuy Le-Tu, Sy Hoang-Van
Department of Internal Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Viet Nam.
Department of Radiology, Ha Noi Medical University, Ha Noi, Viet Nam.
Respir Med Case Rep. 2021 Jul 7;33:101471. doi: 10.1016/j.rmcr.2021.101471. eCollection 2021.
Pulmonary mucoepidermoid carcinoma (PMEC) is an extremely rare tumor of the respiratory system. The clinical presentation of PMEC is variable and nonspecific, including cough, hemoptysis, and wheezing, and may mimic other symptoms of pneumonia or asthma. Here, we present a case of PMEC in a 12-year-old male who was diagnosed with and treated for asthma for 2 years. The patient presented with symptoms of respiratory failure that did not respond to steroids or bronchodilator medications. Chest computed tomography (CT) scans revealed an endotracheal tumor. The patient underwent complete tumor resection, with no signs of recurrence 6 months after treatment.
肺黏液表皮样癌(PMEC)是一种极为罕见的呼吸系统肿瘤。PMEC的临床表现多样且无特异性,包括咳嗽、咯血和喘息,可能与肺炎或哮喘的其他症状相似。在此,我们报告一例12岁男性PMEC病例,该患者曾被诊断为哮喘并接受了2年治疗。患者出现呼吸衰竭症状,对类固醇或支气管扩张剂药物无反应。胸部计算机断层扫描(CT)显示气管内有肿瘤。患者接受了肿瘤全切术,治疗6个月后无复发迹象。