Tan Yang, Yang Peng, Deng Xiaoyu, Tang Yan
Department of Pathology, Dujiangyan Maternal and Child Health Care Hospital, Chengdu, Sichuan 611830, P.R. China.
Department of Pathology, The Third People's Hospital of Chengdu, Chengdu, Sichuan 610031, P.R. China.
Oncol Lett. 2015 Mar;9(3):1273-1277. doi: 10.3892/ol.2015.2871. Epub 2015 Jan 13.
A 44-year-old male presented with progressing cough, dyspnea and hemoptysis due to a tracheal tumor involving the posterior wall of the lower trachea, with severe airway obstruction and coagulopathy. Consequently the patient underwent segmental resection of the trachea with an end-to-end anastomosis. Twenty months after treatment there remained no evidence of endobronchial recurrence at bronchoscopy or imaging studies. The diagnosis was benign tracheal glomus tumor (GT) which is an exceedingly rare mass lesion in the trachea. There are three subtypes: GT proper, glomangioma and glomangiomyoma. The present study describes the clinical and pathological features of glomangioma through a case report and literature review. To the best of our knowledge, this is the fifth report of glomangioma subtype arising from the trachea.
一名44岁男性因气管肿瘤累及气管下段后壁,出现进行性咳嗽、呼吸困难和咯血,伴有严重气道阻塞和凝血病。因此,该患者接受了气管节段切除及端端吻合术。治疗20个月后,支气管镜检查或影像学检查均未发现支气管内复发迹象。诊断为良性气管血管球瘤(GT),这是一种极其罕见的气管肿块病变。它有三种亚型:典型血管球瘤、血管球血管瘤和血管球血管肌瘤。本研究通过病例报告和文献复习描述了血管球血管瘤的临床和病理特征。据我们所知,这是气管起源的血管球血管瘤亚型的第五例报告。