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Acquired Cryptorchidism in a Boy with Disorder of SexDevelopment

机译:性障碍男孩的后天隐睾症发展历程

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摘要

Recently, it has been reported that boys with severe hypospadias are at increased risk for acquired cryptorchidism. The reports suggested that prenatal and postnatal androgen disruption might be correlated with this condition. We experienced a case of ovotesticular disorder of sex development (DSD), which was ultimately diagnosed at surgery for acquired cryptorchidism. Ascent of the scrotal contents of the left side was detected in a 7-yr-old boy with the 46, XX karyotype, who had a history of perineal hypospadias repair. Intraoperative findings revealed the left gonad consisted of 2 segments, and this was histologically diagnosed as ovotestis by biopsy specimen. Resection of the ovarian segment was performed simultaneously. Exploration of the contralateral gonad showed the same findings. This is the first report of acquired cryptorchidism observed in a patient with DSD presenting with ambiguous genitalia.
机译:最近,据报道患有严重尿道下裂的男孩患后天性隐睾症的风险增加。报告表明,产前和产后雄激素的破坏可能与这种情况有关。我们经历了一例性发育的卵睾丸疾病(DSD),该病最终在手术中被诊断为后天性隐睾症。在一个有会阴尿道下裂修复史的7岁男孩中,发现其左侧阴囊含量的上升是一个46岁,XX核型的男孩。术中发现左性腺由2个部分组成,根据活检标本经组织学诊断为卵睾丸。同时切除卵巢段。对侧性腺的探索显示了相同的发现。这是在患有歧义生殖器的DSD患者中观察到的获得性隐睾症的首次报道。

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