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目的:提高对输尿管炎性肌纤维母细胞瘤(IMT)的认识,避免误诊。方法:报告1例发生于输尿管的IMT患儿临床资料。行左侧肾、输尿管和输尿管入口袖口状膀胱部分切除;病理检查诊断为肾脏IMT。结果:随访11个月,未见肿瘤复发和转移。结论:输尿管IMT为少见的良性或低恶性肿瘤,临床无特异性表现,确诊依靠病理检查,手术治疗时应先送病理检查,以避免误诊误治。
Objective: To improve the understanding of ureteral inflammation myofibroblastic tumor (IMT), to avoid misdiagnosis. Methods: One patient with IMT who had ureter was reported. The left kidney, ureter and ureter entrance cuff-like bladder partial resection; pathological diagnosis of renal IMT. Results: Followed up for 11 months, no tumor recurrence and metastasis. Conclusions: Ureteral IMT is a rare benign or malignant tumor with no specific clinical manifestations. Diagnosis depends on pathological examination. Pathological examination should be performed before surgical treatment to avoid misdiagnosis and mistreatment.