Centro de Investigaciones Endocrinológicas (CEDIE-CONICET), División de Endocrinología, Hospital de Niños Ricardo Gutiérrez, Buenos Aires, Argentina.
Clin Endocrinol (Oxf). 2012 May;76(5):698-705. doi: 10.1111/j.1365-2265.2011.04297.x.
The biphasic ontogeny of serum gonadotrophins observed in normal children also exists in girls with gonadal dysgenesis, although with higher levels. However, limited data exist in prepubertal boys with anorchia.
To investigate whether the existence of testicular tissue is required for gonadotrophin downregulation in boys. Secondarily, we analysed the prevalence of high gonadotrophins and its diagnostic value to assess the presence or absence of testes in childhood.
In a retrospective, semi-longitudinal study, we compared serum gonadotrophin levels in 35 boys with anorchia aged 0-18 years, in 29 bilaterally cryptorchid boys with abdominal testes and in 236 normal boys.
In anorchid boys, follicle stimulating hormone (FSH) and luteinizing hormone (LH) were abnormally high in the first months after birth, then decreased progressively. LH decreased more readily than FSH and dropped to normal values in up to 70% of anorchid patients before the usual age of pubertal onset, when both gonadotrophins increased again to very high levels. In cryptorchid boys, FSH was elevated in a significantly (P < 0·0001) lower proportion of cases. Below the age of 6 years, FSH below 2 IU/l ruled out anorchia and LH above 5 IU/l confirmed anorchia with high accuracy. Between 6 and 11 years, FSH or LH levels above 5 IU/l were highly specific for the absence of testes.
The U-shaped pattern of serum gonadotrophins observed in normal males from birth to puberty was also found in anorchid boys, but with gonadotrophin levels considerably elevated. Serum gonadotrophin levels may normalize in anorchid boys during late childhood only to rise again at puberty. The presence of testicular tissue results in restrain of gonadotrophin secretion in most patients, even if the testes are cryptorchid.
正常儿童血清促性腺激素的双相性发育也存在于性腺发育不良的女孩中,尽管水平较高。然而,在无睾症的青春期前男孩中,相关数据有限。
研究睾丸组织的存在是否是男孩促性腺激素下调所必需的。其次,我们分析了高促性腺激素血症的患病率及其诊断价值,以评估儿童期睾丸的存在与否。
在一项回顾性、半纵向研究中,我们比较了 35 名年龄 0-18 岁的无睾症男孩、29 名双侧隐睾伴腹部睾丸的男孩和 236 名正常男孩的血清促性腺激素水平。
在无睾症男孩中,促卵泡激素(FSH)和促黄体生成素(LH)在出生后的头几个月异常升高,然后逐渐下降。LH 比 FSH下降得更快,在大多数无睾症患者达到青春期开始的正常年龄之前,LH 降至正常水平,此时两种促性腺激素再次升高至非常高的水平。在隐睾男孩中,FSH 升高的比例显著(P < 0·0001)较低。在 6 岁以下,FSH 低于 2 IU/l 可排除无睾症,LH 高于 5 IU/l 可准确确认无睾症。在 6-11 岁之间,FSH 或 LH 水平高于 5 IU/l 高度提示睾丸缺失。
从出生到青春期,正常男性血清促性腺激素呈 U 形模式,无睾症男孩也存在这种模式,但促性腺激素水平显著升高。只有在青春期前的后期,无睾症男孩的血清促性腺激素水平才可能恢复正常,然后再次升高。即使睾丸隐睾,睾丸组织的存在也会导致大多数患者的促性腺激素分泌受到抑制。