Sólyom J, Gács G, Keszei K, Láng K, Orley J, Petheö I, Ságodi L
Acta Endocrinol (Copenh). 1987 Jul;115(3):413-8.
We investigated the value of serum levels of adrenal steroids (dehydroepiandrosterone sulphate, testosterone, 17-hydroxyprogesterone, cortisol) in the identification in peripubertal females with late-onset congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Among 68 females (age 3-18 years) with virilization in childhood, peripubertally or postpubertally, we selected 21 girls for an ACTH test by measurement of basal blood-spot or serum 17-hydroxyprogesterone (17-OHP) levels. Eight of 21 patients had supranormal post-ACTH serum 17-OHP concentration (57-153 nmol/l) with low normal cortisol concentration. All of them had supranormal basal and post-ACTH 17-OHP to cortisol ratios. These data show a relatively high incidence (about 12%) of mild 21-hydroxylase deficiency among prepubertal and adolescent girls with virilization. It is concluded that the first step in the investigation of peripubertally virilized girls should be the determination of serum 17-OHP and cortisol. Patients with basal morning 17-OHP concentration and 17-OHP to cortisol ratio above reference range should be given an ACTH test.
我们研究了血清肾上腺类固醇(硫酸脱氢表雄酮、睾酮、17-羟孕酮、皮质醇)水平在鉴别青春期前女性迟发性先天性肾上腺皮质增生症(因21-羟化酶缺乏所致)中的价值。在68名童年期、青春期或青春期后出现男性化的女性(年龄3 - 18岁)中,我们通过测量基础血斑或血清17-羟孕酮(17-OHP)水平,挑选了21名女孩进行促肾上腺皮质激素(ACTH)试验。21名患者中有8名在ACTH刺激后血清17-OHP浓度超常(57 - 153 nmol/L),而皮质醇浓度处于正常低限。她们所有人的基础及ACTH刺激后的17-OHP与皮质醇比值均超常。这些数据表明,在青春期前及青春期出现男性化的女孩中,轻度21-羟化酶缺乏的发生率相对较高(约12%)。结论是,对青春期前后出现男性化的女孩进行检查的第一步应是测定血清17-OHP和皮质醇。基础晨起17-OHP浓度及17-OHP与皮质醇比值高于参考范围的患者应进行ACTH试验。