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对患有明显男性乳房增生症的青春期男孩进行达那唑治疗期间下丘脑-垂体-性腺轴的内分泌学研究。

Endocrinological studies of the hypothalamo-pituitary gonadal axis during danazol treatment in pubertal boys with marked gynecomastia.

作者信息

Beck W, Stubbe P

出版信息

Horm Metab Res. 1982 Dec;14(12):653-7. doi: 10.1055/s-2007-1019110.

Abstract

The present paper evaluates the variations of the hypothalamo-pituitary gonadal axis during Danazol treatment in pubertal boys with marked gynecomastia (breast size more than 6 cm in diameter). Before treatment a normal sleep-dependent gonadotropin increase was found together with a normal response to LHRH stimulation. Plasma prolactin increased at sleep as well. Plasma testosterone values were normal for pubertal age. During Danazol treatment 200 mg daily for 6 months basal gonadotropin levels, the sleep related hormone increases as well as the response to luteinizing-hormone releasing hormone (LHRH) stimulation were blunted. Concomitantly, testosterone values decreased to values seen in pubertal stage II-III. After 6 months of therapy, 4 of 5 boys treated so far, demonstrated a reduction of the gynecomastia to a maximum of 3 cm in diameter. In 1 boy Danazol treatment was finished after 3 months. Because of increased psychological problems a mastectomy was performed. 6 months after cessation of Danazol treatment a normal sleep dependent gonadotropin rhythm and a normal response to LHRH was found again demonstrating a normalization of the physiologic sleep-related gonadotropin rhythms. Plasma testosterone levels nearly increased to values seen before treatment. From the clinical aspect there were no signs of a recurrence of the marked pubertal gynecomastia in all boys treated with Danazol. These results indicate that Danazol is a specific gonadotropin inhibitor acting at the hypothalamo-pituitary level. No side effects on other hormones or on the development of secondary sex characteristics were noted during and after Danazol treatment.

摘要

本文评估了达那唑治疗青春期男性显著男性乳房发育(乳房直径超过6厘米)期间下丘脑-垂体-性腺轴的变化。治疗前,发现睡眠依赖性促性腺激素正常升高,对促性腺激素释放激素(LHRH)刺激反应正常。血浆催乳素在睡眠时也升高。血浆睾酮值在青春期年龄正常。在达那唑治疗期间,每日200毫克,持续6个月,基础促性腺激素水平、与睡眠相关的激素升高以及对促黄体生成素释放激素(LHRH)刺激的反应均减弱。同时,睾酮值降至青春期II-III期所见水平。治疗6个月后,迄今为止接受治疗的5名男孩中有4名男性乳房发育缩小至最大直径3厘米。1名男孩在3个月后结束达那唑治疗。由于心理问题增加,进行了乳房切除术。达那唑治疗停止6个月后,再次发现睡眠依赖性促性腺激素节律正常,对LHRH反应正常,表明生理性睡眠相关促性腺激素节律恢复正常。血浆睾酮水平几乎升至治疗前所见水平。从临床角度看,所有接受达那唑治疗的男孩均未出现明显青春期男性乳房发育复发的迹象。这些结果表明,达那唑是一种作用于下丘脑-垂体水平的特异性促性腺激素抑制剂。在达那唑治疗期间及之后,未观察到对其他激素或第二性征发育的副作用。

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