摘要
目的:探讨输尿管炎性肌纤维母细胞瘤(IMT)的临床病理特征。方法:报道1例输尿管炎性肌纤维母细胞瘤。结果:B超示左输尿管实性包块;免疫组化:SMA(+)S-100(+)Vim(+)。术后随访1年未见复发。结论:输尿管炎性肌纤维母细胞瘤罕见,临床可表现为腹部包块,腹痛,确诊需病理检查及免疫组化。
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