Inflammatory myofibroblastic tumor of the urinary bladder: A rare diagnostic challenge.

IF 1.7 Q3 UROLOGY & NEPHROLOGY
Central European Journal of Urology Pub Date : 2025-01-01 Epub Date: 2025-11-17 DOI:10.5173/ceju.2025.0195
Layla Settaf-Cherif, Adam Ostrowski, Chidindu Chikwendu, Oliwia Kwiatkowska, Michał Czarnogórski, Paweł Lipowski, Kajetan Juszczak, Jan Adamowicz, Tomasz Drewa
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引用次数: 0

Abstract

We present a case of a 44-year-old male with gross hematuria and lower urinary tract symptoms (LUTS). Ultrasonography revealed a 3 cm lesion, initially non-indicative of bladder cancer. Magnetic resonance imaging (MRI) identified a 26 mm posterior bladder wall mass, suggesting muscle invasive bladder cancer (MIBC). Transurethral resection of the bladder tumor (TURBT) was performed. Histopathology and immunohistochemistry confirmed an inflammatory myofibroblastic tumor (IMT). No neuro- or angioinvasion was present. Follow-up clinical evaluation revealed no evidence of recurrence, and the patient remained asymptomatic with complete resolution of urinary symptoms.

膀胱炎性肌纤维母细胞瘤:罕见的诊断挑战。
我们报告一例44岁男性,有肉眼血尿和下尿路症状(LUTS)。超声检查显示一个3厘米的病变,最初没有膀胱癌的迹象。磁共振成像(MRI)发现26毫米膀胱后壁肿块,提示肌性浸润性膀胱癌(MIBC)。经尿道膀胱肿瘤切除术(turt)。组织病理学和免疫组化证实为炎性肌纤维母细胞瘤(IMT)。未见神经或血管侵犯。随访临床评估显示无复发迹象,患者无症状,泌尿系统症状完全消退。
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来源期刊
Central European Journal of Urology
Central European Journal of Urology UROLOGY & NEPHROLOGY-
CiteScore
2.30
自引率
8.30%
发文量
48
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