Wei Li, Jianbo Liang, Qiang Wei, Hai Yu, Zhixiang Lan
Department of Urology, The People's Hospital of Guangxi Zhuang, Autonomous Region, Nanning, China;
Can Urol Assoc J. 2013 Mar-Apr;7(3-4):E237-40. doi: 10.5489/cuaj.544.
Inflammatory myofibroblastic tumour (IMT) is a rare tumour with malignant potential, and has been described in many major organs. However, bladder location is very uncommon. We report the case of a 23-year-old woman who presented with painless gross hematuria for 2 weeks. Contrast-enhanced computed tomography revealed a bladder tumour. The patient underwent an open partial cystectomy and the final pathologic diagnosis was IMT of bladder. Typical IMTs can be locally aggressive, therefore close follow-up is necessary.
炎性肌纤维母细胞瘤(IMT)是一种具有恶性潜能的罕见肿瘤,已在许多主要器官中被描述。然而,膀胱部位非常少见。我们报告一例23岁女性患者,其出现无痛性肉眼血尿2周。增强计算机断层扫描显示膀胱肿瘤。患者接受了开放性部分膀胱切除术,最终病理诊断为膀胱IMT。典型的IMT可能具有局部侵袭性,因此密切随访是必要的。