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伴有多骨纤维发育不良的特发性下丘脑性低促性腺激素性性腺功能减退症。

Idiopathic hypothalamic hypogonadotropic hypogonadism with polyostotic fibrous dysplasia.

作者信息

Shires R, Whyte M P, Avioli L V

出版信息

Arch Intern Med. 1979 Oct;139(10):1187-9.

PMID:485758
Abstract

A 22-year-old woman had polyostotic fibrous dysplasia (POFD) and idiopathic hypothalamic hypogonadotropic hypogonadism (isolated gonadotropin deficiency). Recurrent fracture of dysplastic bone during childhood was associated with primary amenorrhea, clinical and laboratory evidence of estrogen deficiency, and subnormal circulating and urinary gonadotropin levels during adolescence. Gonadorelin (luteinizing hormone-releasing hormone) stimulation initially showed a luteinizing hormone (LH) response but absent follicle-stimulating hormone (FSH) response. After three months without estrogen and progesterone and after four days of gonadorelin "priming," a subsequent gonadorelin infusion produced an enhanced LH and FSH response. All other tests of peripheral and trophic hormone levels and pituitary trophic hormone reserves were normal. Whereas POFD is known to occur with sexual precocity and other endocrinopathies, to our knowledge this is the first report of its association with isolated gonadotropin deficiency.

摘要

一名22岁女性患有多骨型纤维发育不良(POFD)和特发性下丘脑性性腺功能减退症(孤立性促性腺激素缺乏)。儿童期发育异常的骨骼反复骨折,与原发性闭经、雌激素缺乏的临床和实验室证据以及青春期循环和尿促性腺激素水平低于正常有关。促性腺激素释放激素(黄体生成素释放激素)刺激最初显示有黄体生成素(LH)反应,但无卵泡刺激素(FSH)反应。在停用雌激素和孕激素三个月后,以及在促性腺激素释放激素“预激”四天后,随后的促性腺激素释放激素输注产生了增强的LH和FSH反应。外周和促激素水平以及垂体促激素储备的所有其他测试均正常。虽然已知POFD会伴有性早熟和其他内分泌疾病,但据我们所知,这是其与孤立性促性腺激素缺乏相关的首次报告。

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