Li Zuwei, Lin Canbin, Wang Danyun, Xie Jiansen, Zhou Cankun, Chen Peijie, Yang Yu, Sun Shuolei, Peng Jian, Yang Shangqi, Lai Yongqing
Department of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Department of Urology, Shantou University Medical College, Shantou, Guangdong 515041, P.R. China.
Mol Clin Oncol. 2018 Sep;9(3):335-338. doi: 10.3892/mco.2018.1679. Epub 2018 Jul 19.
Primary small-cell neuroendocrine carcinoma (SCNEC) of the urinary bladder is a rare tumor characterized by poor differentiation and high aggressiveness. Only ~150 cases have been reported in the literature to date. We herein present a case of an 87-year-old man who presented with hematuria and was found to have an ill-defined mass in the urinary bladder on computed tomography and cystoscopic examination. On pathological examination following tumor biopsy, the mucosa of the bladder wall was found to be extensively infiltrated by neuroendocrine carcinoma, positive for CD56 and synaptophysin and negative for epithelial membrane antigen, consistent with SCNEC of the urinary bladder. The patient refused further surgical treatment and succumbed to the disease 2 months after the diagnosis. In the present study, this rare case of primary SCNEC of the urinary bladder is presented, along with a discussion on the clinical presentation, immunohistochemical and cytomorphological characteristics, management, biological behavior and prognosis of this disease.
原发性膀胱小细胞神经内分泌癌(SCNEC)是一种罕见肿瘤,其特征为分化差且侵袭性高。迄今为止,文献中仅报道了约150例病例。我们在此报告一例87岁男性,该患者因血尿就诊,经计算机断层扫描和膀胱镜检查发现膀胱内有边界不清的肿块。肿瘤活检后的病理检查显示,膀胱壁黏膜被神经内分泌癌广泛浸润,CD56和突触素呈阳性,上皮膜抗原呈阴性,符合膀胱SCNEC。患者拒绝进一步手术治疗,诊断后2个月死于该疾病。在本研究中,我们展示了这例罕见的原发性膀胱SCNEC病例,并对该疾病的临床表现、免疫组化和细胞形态学特征、治疗、生物学行为及预后进行了讨论。