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Prevalence of late-onset adrenal hyperplasia in postmenarchal hirsutism.

作者信息

Motta P, Catania A, Airaghi L, Mangone I, Cantalamessa L, Zanussi C

机构信息

Clinica Medica I, Università di Milano, Italy.

出版信息

J Endocrinol Invest. 1988 Oct;11(9):675-8. doi: 10.1007/BF03350213.

DOI:10.1007/BF03350213
PMID:2851623
Abstract

The response of plasma 17-hydroxyprogesterone (17-OHP) to exogenous ACTH was investigated in 85 consecutive women referred for postmenarchal hirsutism, in order to assess the prevalence of late-onset adrenal hyperplasia due to 21-hydroxylase deficiency and its relevance to the clinical practice. An exaggerated response of plasma 17-OHP to ACTH, indicating 21-hydroxylase deficiency, was found in only one patient with a prevalence of 1.1%. The patient with late-onset adrenal hyperplasia presented signs of virilism and had high basal levels of 17-OHP. On the basis of our results, late-onset adrenal hyperplasia accounts for a very small proportion of cases of hirsutism; moreover, from this and previous studies it is apparent that the determination of basal plasma 17-OHP may be sufficient to discover late-onset 21-hydroxylase deficiency. Therefore, we do not consider ACTH testing an advisable step in the routine screening for hirsutism.

摘要

相似文献

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引用本文的文献

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本文引用的文献

1
The determination of urinary steroids. I. The preparation of pigment-free extracts and a simplified procedure for the estimation of total 17-ketosteroids.尿甾体的测定。I. 无色素提取物的制备及总17-酮甾体测定的简化程序。
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Clinical assessment of body hair growth in women.女性体毛生长的临床评估
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High frequency of nonclassical steroid 21-hydroxylase deficiency.非经典型类固醇21-羟化酶缺乏症的高发病率。
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5
Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.迟发性21-羟化酶缺乏症,临床表现类似特发性多毛症或多囊卵巢疾病。
Ann Intern Med. 1982 Feb;96(2):143-8. doi: 10.7326/0003-4819-96-2-143.
6
Evidence of excessive androgen secretion by both the ovary and the adrenal in patients with idiopathic hirsutism.特发性多毛症患者卵巢和肾上腺雄激素分泌过多的证据。
Obstet Gynecol. 1982 Jan;59(1):46-51.
7
The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women.多毛女性中因21-羟化酶缺乏所致迟发型先天性肾上腺皮质增生症的发病率。
J Clin Endocrinol Metab. 1984 Apr;58(4):595-8. doi: 10.1210/jcem-58-4-595.
8
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.迟发型类固醇21-羟化酶缺乏症:经典型先天性肾上腺皮质增生症的一种变异型。
J Clin Endocrinol Metab. 1982 Nov;55(5):817-27. doi: 10.1210/jcem-55-5-817.
9
Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.因21-羟化酶缺乏不完全导致的先天性肾上腺增生症的成人表现,酷似多囊卵巢疾病。
Am J Obstet Gynecol. 1980 Nov 15;138(6):720-6. doi: 10.1016/0002-9378(80)90095-2.
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The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
J Clin Endocrinol Metab. 1980 Sep;51(3):647-9. doi: 10.1210/jcem-51-3-647.