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首页> 外文期刊>The Journal of Urology >Histological examination of solitary contralateral descended testis in congenital absence of testis
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Histological examination of solitary contralateral descended testis in congenital absence of testis

机译:先天性睾丸缺如的单侧对侧下降睾丸的组织学检查

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摘要

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.
机译:先天性睾丸缺乏被认为是继发于产前扭转的继发性疾病,与孤立的睾丸未下降的睾丸不同。我们确定了先天性睾丸缺失与单侧对侧睾丸下降的异常组织学是否相关。总共239名主要诊断为单侧无睾丸的男孩接受了睾丸切除术和睾丸活检。在年龄随机匹配的单侧未降睾丸患者中,对孤立的对侧睾丸和对侧睾丸的生殖细胞计数进行了比较。进行了亚组分析,评估了研究组之间的肥大睾丸和肥大青春前睾丸。单侧对侧睾丸下降组表现出明显更大的体积(p <0.001)和明显更大的生殖细胞计数(p = 0.001)。在肥大的睾丸中,有更高的生殖细胞计数(p = 0.02),更高的生殖细胞百分比(p = 0.02),更高的原代精母细胞计数(p = 0.04)和更高的原代精母细胞百分比(p = 0.03)。在成人黑暗精原细胞或Leydig细胞中未检测到显着差异。青春期前患者的原代精母细胞无显着差异。与单侧隐睾症的对侧下降睾丸相比,孤立的对侧下降睾丸表现出增大的体积,增加的生殖细胞增殖和不同的成熟方式。这些发现支持先天性睾丸扭转的产前扭转,而不是内分泌病变。在青春期后的单侧对侧睾丸下降中,可以看到更多的生殖细胞成熟,而原代精母细胞占生殖细胞总数的增加。睾丸孤立的患者可能不存在其他不孕风险。

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