Perisson Caroline, Nathan Nadia, Thierry Briac, Corvol Harriet
Pediatric Pulmonology-INSERM UMR S-938, AP-HP Hôpital Armand Trousseau, Paris, France.
BMJ Case Rep. 2013 Nov 19;2013:bcr2013200776. doi: 10.1136/bcr-2013-200776.
A 12-month-old boy, with no medical history, was admitted for dyspnoea with no cough or fever. Chest auscultation revealed an expiratory wheezing with decreased right-sided breath sounds. Chest imaging revealed subcarinal adenopathy and a nodule in the right principal bronchus (RB). Bronchoscopy showed a major obstruction of the RB by a granuloma, and a smaller granuloma in the left principal bronchus. The granulation tissue was removed by laser section. Histological examination revealed a necrotising granulomatous inflammation, culture showed a Mycobacterium avium complex (MAC). Tests to rule out tuberculosis and immunodeficiency were negative. The diagnosis of an MAC endobronchial granuloma was ascertained and a multidrug therapy associating clarithromycin, rifampin and ethambutol was started. The clinical outcome was good after 3 months of treatment and the bronchoscopy normalised after 1 year. Although rare, the frequency of MAC respiratory infections in immunocompetent children can increase. Reporting these cases should help to optimise diagnosis and treatment.
一名12个月大的男童,无病史,因呼吸困难入院,无咳嗽或发热症状。胸部听诊发现呼气性哮鸣音,右侧呼吸音减弱。胸部影像学检查显示隆突下淋巴结肿大及右主支气管(RB)内有一个结节。支气管镜检查显示RB被肉芽肿严重阻塞,左主支气管内有一个较小的肉芽肿。通过激光切片切除了肉芽组织。组织学检查显示为坏死性肉芽肿性炎症,培养显示为鸟分枝杆菌复合群(MAC)。排除结核病和免疫缺陷的检查均为阴性。确诊为MAC支气管内肉芽肿,并开始使用克拉霉素、利福平和乙胺丁醇联合的多药治疗。治疗3个月后临床结果良好,1年后支气管镜检查恢复正常。尽管罕见,但免疫功能正常儿童中MAC呼吸道感染的发生率可能会增加。报告这些病例应有助于优化诊断和治疗。