Lai Yulin, Xie Jiansen, Tian Peikai, Zhong Liming, Ni Liangchao
Department of Urology, Peking University Shenzhen Hospital, Institute of Urology, Shenzhen PKU-HKUST Medical Center, Shenzhen, Guangdong 518036, P.R. China.
Graduate Institute, Guangzhou Medical University, Guangzhou, Guangdong 511436, P.R. China.
Mol Clin Oncol. 2019 Jan;10(1):97-100. doi: 10.3892/mco.2018.1760. Epub 2018 Nov 8.
The aim of the present study was to discuss the diagnosis and treatment of a patient with true hermaphroditism complicated by seminoma. The patient was a 35-year-old man who was admitted to the Peking University Shenzhen Hospital with a retractable mass in the left inguinal region for 20 years. A computed tomography examination revealed right cryptorchidism. The postoperative pathology suggested true hermaphroditism with a seminoma. The results of immunohistochemical examination were as follows: Sal-like protein 4+ (partially weak); octamer-binding transcription factor 4+ (partially weak); CD117+; cytokeratin+; CD30-, α-fetoprotein-, inhibin-α-. The karyotype was 46, XY. Adult true hermaphroditism combined with seminoma is rare in clinical practice. Combined histopathological analysis, immunophenotype detection and karyotype analysis are of great value in the diagnosis and differential diagnosis. Early intervention and combined surgery with radiotherapy and chemotherapy can significantly improve the prognosis of such patients.
本研究的目的是探讨一名真性两性畸形合并精原细胞瘤患者的诊断与治疗。该患者为一名35岁男性,因左侧腹股沟区可复性肿物20年入住北京大学深圳医院。计算机断层扫描检查显示右侧隐睾。术后病理提示真性两性畸形合并精原细胞瘤。免疫组化检查结果如下:Sal样蛋白4+(部分弱阳性);八聚体结合转录因子4+(部分弱阳性);CD117+;细胞角蛋白+;CD30-、甲胎蛋白-、抑制素-α-。核型为46,XY。成人真性两性畸形合并精原细胞瘤在临床实践中较为罕见。联合组织病理学分析、免疫表型检测和核型分析对诊断和鉴别诊断具有重要价值。早期干预以及手术联合放疗和化疗可显著改善此类患者的预后。