Department of Urology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Saitama, Japan.
Department of Pathology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Saitama, Japan.
Am J Mens Health. 2020 Sep-Oct;14(5):1557988320970071. doi: 10.1177/1557988320970071.
The risk of a gonadal tumor is high in testicular disorder of sexual development (DSD) with the Y chromosome, but cases of DSD without the Y chromosome are extremely rare. We reported a gonadal tumor in a phenotypically male individual with 46, XX testicular DSD. A testicular tumor was incidentally found in a 32-year-old phenotypic male who was presented to the hospital with male infertility. A diagnosis of 46, XX testicular DSD was made by the presentation of karyotype analysis of 46, XX with the sex-determining region of the Y chromosome (SRY) positive and gonadal tissue without female gonads. Surgery was performed due to a gradually growing tumor. The partial orchidectomy was performed with the diagnosis of a benign Leydig cell tumor in frozen biopsy.
性发育障碍(DSD)伴 Y 染色体患者发生性腺肿瘤的风险较高,但不伴 Y 染色体的 DSD 极为罕见。我们报告了 1 例表型男性 46,XX 睾丸 DSD 患者发生性腺肿瘤。1 名 32 岁表型男性因男性不育就诊时偶然发现睾丸肿瘤。该患者核型分析为 46,XX,Y 染色体性别决定区(SRY)阳性,性腺组织无女性性腺,诊断为 46,XX 睾丸 DSD。由于肿瘤逐渐增大,故进行了手术。冷冻活检诊断为良性 Leydig 细胞瘤,行部分睾丸切除术。