Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
J Urol. 2012 Feb;187(2):676-80. doi: 10.1016/j.juro.2011.10.021. Epub 2011 Dec 16.
Congenital absence of the testis is believed to be secondary to prenatal torsion, differing from the isolated undescended testis. We determined whether congenital absence of the testis is associated with abnormal histology in the solitary contralateral descended testis.
A total of 239 boys with a primary diagnosis of unilateral absent testis underwent orchiectomy and testis biopsy. Germ cell counts were compared between solitary contralateral descended testes and contralateral descended testes in a randomly selected, age matched cohort of patients with unilateral undescended testes. Subanalyses evaluating hypertrophic testes and hypertrophic prepubertal testes between the study groups were performed.
The solitary contralateral descended testis group exhibited a significantly greater volume (p <0.001) and a significantly greater germ cell count (p = 0.001). In the hypertrophied testes there was a greater gonocyte count (p = 0.02), greater percentage of gonocytes (p = 0.02), greater primary spermatocyte count (p = 0.04) and greater percentage of primary spermatocytes (p = 0.03). No significant differences in adult dark spermatogonia or Leydig cells were detected. Primary spermatocytes did not differ significantly in prepubertal patients.
The solitary contralateral descended testis exhibits increased volume, increased germ cell proliferation and dissimilar maturation patterns compared to the contralateral descended testis in unilateral cryptorchidism. These findings support prenatal torsion rather than endocrinopathy as the etiology for the congenitally absent testis. In the postpubertal solitary contralateral descended testis more germ cell maturation is seen and primary spermatocytes account for the increased total germ cell count. Patients with a solitary testis are likely not at additional risk for infertility.
先天性睾丸缺失被认为是产前扭转的继发原因,与孤立性未降睾丸不同。我们确定先天性睾丸缺失是否与单侧隐睾对侧下降睾丸的异常组织学有关。
共有 239 名患有单侧无睾症的男孩接受了睾丸切除术和睾丸活检。在单侧未降睾丸的随机选择、年龄匹配的患者队列中,比较了对侧下降睾丸和对侧下降睾丸的生精细胞计数。对研究组之间的肥大睾丸和青春期前肥大睾丸进行了亚分析。
孤立的对侧下降睾丸组表现出明显更大的体积(p <0.001)和明显更高的生精细胞计数(p = 0.001)。在肥大睾丸中,有更多的精原细胞计数(p = 0.02),更多的精原细胞百分比(p = 0.02),更多的初级精母细胞计数(p = 0.04)和更多的初级精母细胞百分比(p = 0.03)。在成年暗精原细胞或睾丸间质细胞中未发现显著差异。青春期前患者的初级精母细胞无显著差异。
与单侧隐睾对侧下降睾丸相比,单侧隐睾对侧下降睾丸的体积增大、生殖细胞增殖增加且成熟模式不同。这些发现支持产前扭转而不是内分泌异常是先天性睾丸缺失的病因。在青春期后,对侧下降睾丸中更多的生殖细胞成熟,并且初级精母细胞占增加的总生殖细胞计数。单侧隐睾的患者不太可能有额外的不育风险。