Boloursaz M R, Khalilzadeh S, Abbasi Dezfoli A, Kahkoee Sh, Karimi Sh, Abbaszadeh M, Masjedi M R, Velayati A A
Pediatric Respiratory Disease Research Center, National Research Institue of Tuberculosis and Lung Disease, Masih Daneshvari Hospital, Shaheed Beheshti University of Medical Science, Tehran, Iran.
Pneumologia. 2010 Oct-Dec;59(4):215-6.
This report described a 2-year-old boy who presented with severe respiratory distress and stridor. Bronchoscopy and CT revealed a mass in the left anterolateral tracheal wall and histopathology showed a tracheal inflammatory myofibroblastic tumor. Initial removal by rigid bronchoscopy resulted in prompt recurrence of the tumor. Therefore he underwent tracheal surgical resection. A bronchoscopy at 12 months after surgery did not show any recurrence sign.
本报告描述了一名2岁男孩,他出现严重呼吸窘迫和喘鸣。支气管镜检查和CT显示左前外侧气管壁有一个肿块,组织病理学显示为气管炎性肌纤维母细胞瘤。最初通过硬质支气管镜切除导致肿瘤迅速复发。因此,他接受了气管手术切除。术后12个月的支气管镜检查未显示任何复发迹象。