摘要
炎性肌纤维母细胞瘤(inflammatory myofibroblastic tumor,IMT)是一种罕见的间叶性来源的肿瘤,本文报道1例小儿男性气管腔内IMT,结合文献复习该疾病的临床特点、诊断、治疗及预后,并进行IMT与错构瘤的鉴别诊断以最终确诊该患儿肿瘤性质。
Inflammatory myofibroblastic tumor is a rare tumor of mesenchymal origin.A case of intratracheal inflammatory myofibroblastic tumor in a male child was reported.The clinical characteristics,diagnosis,treatment and prognosis of the disease were reviewed based on the literature,and a differential diagnosis between inflammatory myofibroblastic tumor and hamartoma was performed to ultimately confirm the nature of the tumor in the child.
作者
覃时超
魏东敏
徐晨阳
苏同东
雷大鹏
QIN Shichao;WEI Dongmin;XU Chenyang;SU Tongdong;LEI Dapeng(Department of Otorhinolaryngology,Qilu Hospital of Shandong University,National Health Commission Key Laboratory of Otorhinolaryngology,Ji'nan,250012,China)
出处
《临床耳鼻咽喉头颈外科杂志》
CAS
CSCD
北大核心
2023年第10期840-842,共3页
Journal of Clinical Otorhinolaryngology Head And Neck Surgery
关键词
炎性肌纤维母细胞瘤
气管
儿童
inflammatory myofibroblastic tumor
trachea
children
