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SRY-Positive 46 XX Testicular Disorder of Sexual Development With Leydig Cell Tumor

机译:Sry-阳阳性46XX睾丸性发育病症与leydig细胞肿瘤

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摘要

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.
机译:随着Y染色体的性发育睾丸障碍(DSD)的睾丸病症的风险很高,但没有Y染色体的DSD病例非常罕见。我们在表型雄性个体中报道了一种具有46,XX睾丸DSD的Gonadal肿瘤。睾丸肿瘤偶然发现,在32岁的表型男性中,患有男性不孕症的医院。通过呈现46,XX的核型分析,XX睾丸DSD诊断为46,XX与Y染色体(SRY)阳性和GONADAL组织的性别测定区域而没有女性性腺。由于逐渐生长的肿瘤而进行手术。在冷冻活检中诊断良性Leydig细胞肿瘤进行部分植物切除术。

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