Department of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China.
BMC Med Genomics. 2022 Sep 5;15(1):188. doi: 10.1186/s12920-022-01347-0.
46,XX male disorders of sex development are rare. Approximately 80% of cases of testicular tissue differentiation may be due to translocation of SRY to the X chromosome or an autosome. SRY-negative 46,XX males show overexpression of pro-testis genes, such as SOX9 and SOX3, or failure of pro-ovarian genes, such as WNT4 and RSPO1, which induces testis differentiation, however, almost all testicles exhibit dysgenesis. Following inadequate exposure to androgens during the embryo stage, remnants of the Mullerian duct and incomplete closure of the urogenital sinus lead to enlargement of prostatic utricles. This condition is associated with proximal hypospadias and disorders of sex development. Many cases are asymptomatic, but show increased rates of postoperative complications and surgical failure.
A 5-year-old Chinese boy with scrotal hypospadias and bilateral cryptorchidism with prostatic utricles was presented. Gonadal histology showed ovo-testicular tissue on the right side and testicular tissue on the left side; all testicular tissue exhibited dysgenesis. Furthermore, chromosome karyotype analysis revealed 46,XX and, the presence of SRY was ruled out by polymerase chain reaction analysis. Whole-genome analysis showed the boy has a 1.4-Mb duplication in the Xq27.1q27.2 region (arr[hg19]Xq27.1q27.2:139585794-140996652) involving SOX3. No SOX3 duplication was observed in the parents, who had a normal phenotype.
We report the first case of an SRY-negative 46 XX male with prostatic utricle caused by SOX3 duplication. SOX3 duplication may cause sex reversal, and all 46,XX SRY-negative males should be screened for SOX3 mutations. Gonadal biopsy is recommended to evaluate ovarian and testicular tissue development. Testicular dysgenesis and low exposure to male hormones during fetal development can lead to enlarged prostatic utricles. Thus endoscopic examination should be performed preoperatively to detect prostatic utricles in SRY-negative 46,XX males to determine the surgical plan and reduce postoperative complications.
46,XX 男性性发育障碍较为罕见。大约 80%的睾丸组织分化病例可能是由于 SRY 易位到 X 染色体或常染色体上。SRY 阴性 46,XX 男性表现出促睾丸基因如 SOX9 和 SOX3 的过度表达,或促卵巢基因如 WNT4 和 RSPO1 的失活,这些基因会诱导睾丸分化,但几乎所有睾丸都表现出发育不良。在胚胎期雄激素暴露不足后,苗勒管的残余物和尿生殖窦的不完全闭合导致前列腺囊的增大。这种情况与近端尿道下裂和性发育障碍有关。许多病例无症状,但术后并发症和手术失败的发生率增加。
一名 5 岁的中国男孩,表现为阴囊型尿道下裂和双侧隐睾伴前列腺囊增大。性腺组织学检查显示右侧为卵睾组织,左侧为睾丸组织;所有睾丸组织均表现为发育不良。此外,染色体核型分析显示为 46,XX,聚合酶链反应分析排除了 SRY 的存在。全基因组分析显示该男孩 Xq27.1q27.2 区域存在 1.4-Mb 重复(arr[hg19]Xq27.1q27.2:139585794-140996652),涉及 SOX3。父母均无表型异常,未观察到 SOX3 重复。
我们报告了首例由 SOX3 重复引起的 SRY 阴性 46 XX 男性伴前列腺囊增大的病例。SOX3 重复可能导致性别反转,所有 46,XX SRY 阴性男性都应筛查 SOX3 突变。建议进行性腺活检以评估卵巢和睾丸组织发育。胎儿发育过程中睾丸发育不良和雄激素暴露不足可导致前列腺囊增大。因此,术前应进行内镜检查以检测 SRY 阴性 46,XX 男性的前列腺囊,以确定手术计划并减少术后并发症。