Otsuki Hideo, Ito Keiichi, Sato Ken, Kosaka Takeo, Shimazaki Hideyuki, Kaji Tatsumi, Asano Tomohiko
Departments of Urology, Tokorozawa, Saitama 359-8513, Japan.
Oncol Lett. 2013 May;5(5):1625-1628. doi: 10.3892/ol.2013.1221. Epub 2013 Mar 1.
Mucosa-associated lymphoid tissue (MALT) lymphoma occurs in various sites, but rarely in the urinary tract. Imaging studies of a 69-year-old male revealed a left hydronephrosis and diffuse thickening of the renal pelvic and upper ureteral wall. Retrograde pyelography revealed a narrowing in this region, and brush cytology specimens contained atypical cells. As the lesion was considered to be malignant, surgical excision was performed. Histological analysis revealed an intense lymphoid infiltrate mainly consisting of B cells. The immunohistochemistry results demonstrated that the lesion was positive for CD20 and CD79a and negative for CD5 and cyclin D1. These findings led to a diagnosis of MALT lymphoma. Pathological exploration disclosed a focally dense invasion of lymphoma cells into not only the renal pelvis, but the whole ureteral wall and surrounding tissue; therefore, the patient underwent eight courses of rituximab treatment. Diffuse invasion of lymphoma cells into the whole ureter was rarely observed. Since the surgery, the patient has survived for 78 months without evidence of a recurrence of lymphoma.
黏膜相关淋巴组织(MALT)淋巴瘤可发生于多个部位,但很少发生于泌尿系统。一名69岁男性的影像学检查显示左肾积水以及肾盂和输尿管上段壁弥漫性增厚。逆行肾盂造影显示该区域狭窄,刷检细胞学标本中含有非典型细胞。由于该病变被认为是恶性的,遂进行了手术切除。组织学分析显示主要由B细胞组成的密集淋巴细胞浸润。免疫组化结果表明,该病变CD20和CD79a呈阳性,CD5和细胞周期蛋白D1呈阴性。这些发现导致诊断为MALT淋巴瘤。病理检查发现淋巴瘤细胞不仅局灶性密集浸润肾盂,还浸润整个输尿管壁及周围组织;因此,该患者接受了8个疗程的利妥昔单抗治疗。淋巴瘤细胞弥漫性浸润整个输尿管的情况很少见。自手术以来,该患者已存活78个月,无淋巴瘤复发迹象。