Costa Susana, Chacim Sérgio, Oliveira Ângelo, Castro Carla
Radiation Oncology, Instituto Português de Oncologia do Porto, Porto, PRT.
Hematology, Instituto Português de Oncologia do Porto, Porto, PRT.
Cureus. 2024 May 23;16(5):e60885. doi: 10.7759/cureus.60885. eCollection 2024 May.
Primary lymphoma of the urinary bladder is extremely rare. We present the case of a 67-year-old woman diagnosed with primary extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) of the urinary bladder. The patient presented with macroscopic hematuria. Renal ultrasound revealed a solid vascularized mass, in the inferior wall of the bladder. Pelvic computed tomography (CT) and magnetic resonance imaging (MRI) confirmed the presence of a polypoid lesion on the left side of the inferior bladder wall, measuring 40x45 mm, and the MRI study with gadolinium revealed that the entire bladder wall was involved. The patient underwent transurethral resection of the bladder tumor, demonstrating a histologic extensive involvement of bladder tissue by MALT lymphoma. The patient was treated with radiotherapy (24 Gy in 12 fractions) and four cycles of rituximab. She remained without evidence of disease 12 months later.
原发性膀胱淋巴瘤极为罕见。我们报告一例67岁女性,被诊断为原发性膀胱黏膜相关淋巴组织(MALT)结外边缘区淋巴瘤。患者出现肉眼血尿。肾脏超声显示膀胱下壁有一个实性血管化肿块。盆腔计算机断层扫描(CT)和磁共振成像(MRI)证实膀胱下壁左侧存在一个息肉样病变,大小为40×45 mm,钆增强MRI研究显示整个膀胱壁均受累。患者接受了经尿道膀胱肿瘤切除术,病理显示MALT淋巴瘤广泛侵犯膀胱组织。患者接受了放射治疗(12次分割,共24 Gy)和四个周期的利妥昔单抗治疗。12个月后,她没有疾病复发的迹象。