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SRY 阳性 46,XX 性发育障碍伴睾丸间质细胞瘤。

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

机构信息

Department of Urology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Saitama, Japan.

Department of Pathology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Saitama, Japan.

出版信息

Am J Mens Health. 2020 Sep-Oct;14(5):1557988320970071. doi: 10.1177/1557988320970071.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/7607790/e8b4e105ff61/10.1177_1557988320970071-fig1.jpg

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