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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。Abstract: 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.
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Key words:
- inflammatory myofibroblastic tumor /
- trachea /
- children
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