真两性畸形伴隐睾原位生殖细胞肿瘤合并性腺母细胞瘤1例报告并文献复习  

Cryptorchidism in true hermaphroditism with a combination of germ cell neoplasia in situ(GCNIS)with gonadoblastoma:a case report and literature review

作　　者：周大鹏 荆翌峰[1] 韩邦旻[1] 孙娟娟 师晓琴 高峰[2] 郭文焕[2] Zhou Dapeng;Jing Yifeng;Han Bangmin;Sun Juanjuan;Shi Xiaoqin;Gao Feng;Guo Wenhuan(Department of Urology,Shanghai First People's Hospital,Shanghai Jiaotong University,Shanghai 200080;Department of Pathology,Shanghai First People's Hospital,Shanghai Jiaotong University,Shanghai 200080)

机构地区：[1]上海交通大学附属第一人民医院泌尿外科,上海200080 [2]上海交通大学附属第一人民医院病理科,上海200080

出　　处：《中国男科学杂志》2020年第3期51-53,共3页Chinese Journal of Andrology

摘　　要：目的探讨真两性畸形伴隐睾原位生殖细胞肿瘤合并性腺母细胞瘤的临床病理特点。方法对上海市第一人民医院1例真两性畸形伴隐睾原位生殖细胞母肿瘤合并性腺细胞瘤患者进行回顾性分析。结果患者为真两性畸形,社会性别女性,术后隐睾病理检查示原位生殖细胞肿瘤合并性腺母细胞瘤。结论真两性畸形是一种少见的DSD,真两性畸形患者隐睾发生原位生殖细胞肿瘤合并性腺母细胞瘤更为罕见。通过对罕见病的分析总结,有利于提高临床诊疗水平。Objective To investigate the clinicopathological characteristics of true hermaphroditism combined with with germ cell neoplasia in situ(GCNIS)combined with gonadoblastoma.Methods A case of cryptorchidism diagnosed with germ cell tumor in Shanghai First People's hospital was analyzed retrospectively.Results The patient was true hermaphroditism and female of social gender.The pathological examination of cryptorchidism showed GCNIS combined with gonadoblastoma.Conclusions True hermaphroditism is a rare form of DSD,especially with GCNIS combined with gonadoblastoma in cryptorchidism.Through the analysis and summary of this rare disease,it is helpful to improve the level of clinical diagnosis and treatment.

关 键 词：卵睾性 性发育疾病 肿瘤 生殖细胞和胚胎性 性腺母细胞瘤 

分 类 号：R736.8[医药卫生—肿瘤]