Djurhuus Bjarki Ditlev, Krogdahl Annelise Solveig, Godballe Christian
Øre-Naese-Halskirurgisk Afdeling, Odense Universitetshospital, 5000 Odense C.
Ugeskr Laeger. 2010 Jul 5;172(27):2040-1.
Paraganglioma with tracheal location is a rare tumor. Twelve cases with involvement of the trachea have been reported in English literature, including six cases of solely tracheal paragangliomas. We present a case of a paraganglioma confined to the tracheal wall in a 33-year-old pregnant woman. The tumor was locally resected. Follow-up 17 months later showed no evidence of relapse. Based on the literature, we found that the most common symptoms are respiratory impairment and haemoptysis. None of the cases showed malignant behaviour.
气管部位的副神经节瘤是一种罕见肿瘤。英文文献中已报道12例累及气管的病例,其中包括6例单纯气管副神经节瘤。我们报告一例33岁孕妇的局限于气管壁的副神经节瘤病例。该肿瘤进行了局部切除。17个月后的随访显示无复发迹象。基于文献,我们发现最常见的症状是呼吸功能障碍和咯血。所有病例均未表现出恶性行为。