Dong Chunge, Yang Youping, Wu Siying, Chen Guorong
Department of Pathology, The First People Hospital of Wenling, Wenling, 317500, China.
J Cancer Res Ther. 2015 Jul-Sep;11(3):663. doi: 10.4103/0973-1482.144653.
Villous adenoma is a rare primary tumor of the urinary system, especially the bladder and kidneys. This study presents two cases of right pelvis villous adenoma, including that of a 61-year-old patient who had experienced hematuria for more than 1 year and was diagnosed with bladder and ureteral stones via B-ultrasound examination, and the other one involving a 65-year-old patient who was hospitalized for 6 days due to a right upper quadrant mass and diagnosed with right renal pelvis stones and hydrops via B-ultrasound examination. Both patients underwent nephrectomy, and their histological analysis demonstrated papillary projections covered by columnar cells and goblet cells. The first patient had a large amount of renal pelvis mucus accumulation with obvious microscopic intestinal metaplasia and mild-moderate nuclear atypia. Immunohistochemical studies revealed positive carcinoembryonic antigen and the caudal type homeobox 2 staining with varying degrees of cytokeratin (CK)-7 and CK20 expression in both patients. Recurrences or metastasis was not observed during the follow-up period of 3-4 years.
绒毛状腺瘤是泌尿系统罕见的原发性肿瘤,尤其是膀胱和肾脏。本研究报告了两例右肾盂绒毛状腺瘤病例,其中一例为61岁患者,有1年多的血尿病史,经B超检查诊断为膀胱和输尿管结石;另一例为65岁患者,因右上腹肿块住院6天,经B超检查诊断为右肾盂结石和积水。两名患者均接受了肾切除术,组织学分析显示乳头状突起被柱状细胞和杯状细胞覆盖。首例患者肾盂有大量黏液积聚,镜下可见明显的肠化生和轻至中度核异型性。免疫组化研究显示,两名患者癌胚抗原和尾型同源盒2染色均呈阳性,细胞角蛋白(CK)-7和CK20表达程度各异。在3至4年的随访期内未观察到复发或转移。