Wierman M E, Beardsworth D E, Mansfield M J, Badger T M, Crawford J D, Crigler J F, Bode H H, Loughlin J S, Kushner D C, Scully R E
N Engl J Med. 1985 Jan 10;312(2):65-72. doi: 10.1056/NEJM198501103120201.
Recent evidence suggests that a group of children exists in whom premature sexual maturation occurs in the absence of pubertal levels of gonadotropins; that is, they have gonadotropin-independent precocious puberty. We compared six boys and one girl with this disorder with four boys and five girls with central precocious puberty, in which there is a pubertal pattern of gonadotropin release. The two groups were similar in age of onset, degree of sexual development, growth velocity, and rate of skeletal maturation. A family history of precocity was noted in four of the boys with gonadotropin-independent precocity, and the girl had McCune-Albright syndrome. Children with central precocious puberty demonstrated a pulsatile release of gonadotropins, pubertal responses to luteinizing hormone-releasing hormone, and complete suppression of gonadarche after exposure to an analogue of luteinizing hormone-releasing hormone (LHRHa). In contrast, children with gonadotropin-independent precocity demonstrated an absence of gonadotropin pulsations, variable responses to luteinizing hormone-releasing hormone, lack of suppression of puberty in response to LHRHa, and cyclic steroidogenesis. Tissue from testicular biopsies performed in five of six boys with gonadotropin-independent precocity showed a range from incipient pubertal development of the tubules with proliferation of Leydig cells to the appearance of normal adult testes. We conclude that gonadotropin-independent precocious puberty is a distinct syndrome, of unknown cause, that may be familial and may have been responsible for many previously reported cases of precocious puberty.
最近的证据表明,存在一组儿童,他们在促性腺激素未达到青春期水平的情况下就出现了性早熟;也就是说,他们患有非促性腺激素依赖性性早熟。我们将6名患有这种疾病的男孩和1名女孩与4名患有中枢性性早熟的男孩和5名女孩进行了比较,中枢性性早熟存在促性腺激素释放的青春期模式。两组在发病年龄、性发育程度、生长速度和骨骼成熟速率方面相似。在4名患有非促性腺激素依赖性性早熟的男孩中有早熟家族史,该女孩患有McCune-Albright综合征。中枢性性早熟的儿童表现出促性腺激素的脉冲式释放、对促黄体生成素释放激素的青春期反应,以及在接触促黄体生成素释放激素类似物(LHRHa)后性腺发育完全受到抑制。相比之下,非促性腺激素依赖性性早熟的儿童表现出促性腺激素无脉冲、对促黄体生成素释放激素反应不一、对LHRHa无青春期抑制反应以及周期性类固醇生成。在6名患有非促性腺激素依赖性性早熟的男孩中,有5名进行了睾丸活检,组织学表现从曲细精管开始出现青春期发育伴有Leydig细胞增生到正常成年睾丸的外观不等。我们得出结论,非促性腺激素依赖性性早熟是一种病因不明的独特综合征,可能具有家族性,可能是许多先前报道的性早熟病例的病因。