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普拉德-拉布哈特-威利综合征的青春期发育

Pubertal development in the Prader-Labhart-Willi syndrome.

作者信息

Kauli R, Prager-Lewin R, Laron Z

出版信息

Acta Paediatr Scand. 1978 Nov;67(6):763-7. doi: 10.1111/j.1651-2227.1978.tb16258.x.

Abstract

The sexual maturation in the Prader-Labhart-Willi (PLW) syndrome was investigated in 14 patients, 10 females and 4 males. A wide variability in the pattern of pubertal development was found including delayed puberty in 5 patients and normal puberty in 4 patients; sexual precocity was also observed in 5 patients, true precocious puberty in one patient and incomplete sexual precocity in the form of precocious pubarche in 4 patients. In 5 patients, 3 of them with precocious pubarche, the appearance of the pubertal signs was followed by a delay or arrest in their future development. An LH-RH stimulation test was performed in 11 patients. In the 6 patients who eventually developed normal puberty, the basal levels and the peak responses of both LH and FSH were within the range of those observed in normal controls of the same pubertal stage. In 4 patients showing marked delay or arrest of puberty, the basal levels were normal or low and the responses of LH and FSH to LH-RH were blunted. Priming with repeated LH-RH stimulation in one of the male patients led to an augmented LH response, suggesting a hypothalamic hypogonadotrophism. It is concluded that the lack of uniformity in the pattern of sexual maturation in the PLW syndrome is due to a variability in the location and extent of a hypothalamic lesion, which may comprise an active process continuing beyond the perinatal period.

摘要

对14例普拉德-拉巴哈特-威利(PLW)综合征患者(10例女性,4例男性)的性成熟情况进行了研究。发现青春期发育模式存在广泛差异,包括5例青春期延迟、4例青春期正常;还观察到5例性早熟,其中1例为真性性早熟,4例为以阴毛早现为形式的不完全性早熟。在5例患者中,3例有阴毛早现,其青春期体征出现后未来发育延迟或停滞。对11例患者进行了促性腺激素释放激素(LH-RH)刺激试验。在最终青春期发育正常的6例患者中,促黄体生成素(LH)和促卵泡生成素(FSH)的基础水平及峰值反应均在同一青春期阶段正常对照者的观察范围内。在4例青春期明显延迟或停滞的患者中,基础水平正常或偏低,LH和FSH对LH-RH的反应迟钝。对1例男性患者反复进行LH-RH刺激激发后,LH反应增强,提示下丘脑促性腺激素功能减退。结论是,PLW综合征性成熟模式缺乏一致性是由于下丘脑病变的位置和范围存在差异,这可能是一个持续到围生期之后的活跃过程。

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