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[男性化综合征与多毛症]

[Virilization syndrome and hirsutism].

作者信息

Takayanagi R, Nawata H

机构信息

Third Department of Internal Medicine, Faculty of Medicine, Kyushu University.

出版信息

Nihon Rinsho. 1997 Nov;55(11):2887-92.

PMID:9396282
Abstract

Severe virilization syndrome is seen in testosterone-producing ovarian or adrenal tumor while symptom in late-onset congenital adrenal hyperplasia (CAH) are usually mild hirsutism and amenorrhea. We determined the serum levels of 17 alpha-hydroxy pregnenolone (17P5) and 17 alpha-hydroxyprogesterone (17P4) 60 min after the intravenous injection of 250 micrograms of ACTH in 10 normal Japanese females with age ranging from 18 to 29 years old. In this test, 1 mg of dexamethasone had been administered orally at 11 p.m. on the previous day to suppress the effect of endogenous ACTH. The ratio of 17P5 to 17P4 was 10.0 +/- 3.6 (mean +/- SD). Five females with hirsutism of no ovarian origin showed normal responses to this rapid ACTH test, suggesting that the incidence of the late-onset CAH is not so high as reported previously.

摘要

严重男性化综合征可见于分泌睾酮的卵巢或肾上腺肿瘤,而迟发性先天性肾上腺皮质增生症(CAH)的症状通常为轻度多毛症和闭经。我们测定了10名年龄在18至29岁之间的正常日本女性静脉注射250微克促肾上腺皮质激素(ACTH)60分钟后的血清17α-羟孕烯醇酮(17P5)和17α-羟孕酮(17P4)水平。在该试验中,前一天晚上11点口服1毫克地塞米松以抑制内源性ACTH的作用。17P5与17P4的比值为10.0±3.6(平均值±标准差)。5名无卵巢源性多毛症的女性对该快速ACTH试验反应正常,提示迟发性CAH的发病率并不像先前报道的那么高。

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