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特发性下丘脑性性腺功能减退伴多骨型纤维性发育不良:1例报告

Idiopathic hypothalamic hypogonadism with polyostotic fibrous dysplasia: report of a case.

作者信息

Huang T S, Chang C C, Lai S M, Chen F W

机构信息

Department of Medicine, National Taiwan University Hospital, Taipei, R.O.C.

出版信息

J Formos Med Assoc. 1990 Apr;89(4):310-3.

PMID:1976749
Abstract

A 48-year-old man with Albright's syndrome and hypogonadism is presented. Eunuchoid status, hypogenitalia and hypogonadotropinemia were associated with pathological fracture and deformity of bones. GnRH test revealed minimal LH response and delayed FSH peak. After pulsatile GnRH priming, the LH response to GnRH increased. Results of other provocative hypothalamic-pituitary tests were consistent with hypothalamic lesions. To the best of our knowledge, this is the first report of a male patient with Albright's syndrome and idiopathic hypothalamic hypogonadism. The hypothesis of endocrinopathy and its relation to other components of this syndrome were reviewed.

摘要

本文报告了一名患有奥尔布赖特综合征和性腺功能减退的48岁男性。类无睾状态、生殖器发育不全和促性腺激素缺乏血症与病理性骨折和骨骼畸形相关。促性腺激素释放激素(GnRH)试验显示促黄体生成素(LH)反应极小且促卵泡生成素(FSH)峰值延迟。在脉冲式GnRH激发后,LH对GnRH的反应增强。其他下丘脑 - 垂体激发试验结果与下丘脑病变一致。据我们所知,这是首例关于患有奥尔布赖特综合征和特发性下丘脑性腺功能减退男性患者的报告。本文对内分泌病假说及其与该综合征其他组成部分的关系进行了综述。

相似文献

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Hypothalamic hypogonadism.下丘脑性性腺功能减退
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