[一种新的抗促性腺激素治疗性早熟和青春期女性乳房发育症[作者译]。

W Swoboda, E Turnheim, H Frisch, J Spona
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引用次数: 0

摘要

从睾酮(异恶唑-乙酯酮)中提取的合成类固醇化合物丹那唑具有促性腺激素抑制活性,用于治疗4例特发性性早熟(2 1/2至4岁)和10例严重青春期女性乳房发育。在性早熟中,对月经和乳房增大的抑制效果较好,而对纵向生长加速和骨成熟的抑制效果不如醋酸环丙孕酮。大多数患有妇科乳房发育症的男孩在几周或几个月内出现明显的乳房增大消退。不同剂量(性早熟患者200- 300mg /天,女性乳房发育患者300- 400mg /天)血浆激素水平(LH、FSH、孕酮、雌二醇、睾酮)变化均在无显著性变化范围内。睾丸激素的下降似乎是一个相当规律的发现。在研究的14名患者中没有发现药物的不良副作用。总之,到目前为止,与用于治疗同性性早熟的化合物相比,达纳唑没有显示出任何优势。相反,这种药物被证明对青春期男性乳房发育症有效,这种情况在严重程度上肯定需要药物治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A new antigonadotropin in the treatment of precocious puberty and pubertal gynaecomastia (author's transl)].

A synthetic steroid compound derived from testosteron (isoxazol-ethisterone), Danazol, with gonadotropin-depressing activity, was used in the treatment of 4 cases of idiopathis sexual precocity (age 2 1/2 to 4 years) and in 10 cases of severe pubertal gynaecomastia. In sexual precocity the suppression of menstruation as well as of breast-enlargement was good, while the suppression of acceleration of longitudinal growth and bone maturation was inferior compared with cyproteron-acetate. In most boys with gynaecomastia a marked regression of breast enlargement occurred within a few weeks or months. With the dosage used (200-300 mg/day in the sexual precocity patients, 300-400 mg in the gynaecomastia patients) the changes in plasma hormone levels (LH, FSH, progesterone, estradiol, testosterone) were within a non significant range. Depression of testosterone seemed to be a rather regular finding. No untoward side-effects of the medication were noticed in the 14 patients studied. In summary, Danazol did not show any advantages compared with the compounds used in the treatment of isosexual precocity sofar. In contrast, the drug proved to have useful effects in pubertal gynecomastia, a condition which in severe degrees certainly deserves medical treatment.

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