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[女性男性化的生物学参数]

[Biological parameters of virilism in women].

作者信息

Botella-Llusiá J, Tresguerres J A, Vaticón M D, Ruiz-González M C, Martin-Santos F J, Guadalix F J, Novo Dominguez A

出版信息

Ann Endocrinol (Paris). 1978;39(6):439-49.

PMID:747380
Abstract

Comparative results of the suppression-stimulation test by dexamethasone and chorionic gonadotropin, chromatographic separation of 17-ketosteroids, and plasma testosterone levels in the ovarian and adrenal veins, in cases of virilism in women. Thirteen patients with hirsutism and virilization were investigated as follows: 1. measurement of plasma testosterone (T) levels by radioimmunoassay (RIA) during suppression-stimulation tests by the administration of Dexamethasone (DXM) and chorionic Gonadotropin (HCG). 2. chromatographic determination of urinary 17-ketosteroids, pregnanediol (P2), and pregnanetriol (P3). An attempt was made to classify virilism as "ovarian" or "adrenal" based on the results of 1. and 2. 3. bilateral ovarian and adrenal venous catheterization through the femoral vein to measure T (RIA) levels. 4. laparotomy with bilateral wedge resections of the ovaries for therapeutic and biopsy purposes. Surgical catheterization of the ovarian veins was carried out during the operation. The results of these tests show that: a) the dynamic DXM-HCG test can be used to separate those cases in which the ovary is not involved in T formation from those in which, apparently, it is involved. b) chromatographic determination of urinary steroids has no aetiological value, as the variations in the different fractions are not significant. c) in all patients, the principal source of T is the adrenals and not the ovaries, even when there is an increase in T in the ovarian efferent blood vessels.

摘要

女性男性化病例中地塞米松和绒毛膜促性腺激素抑制 - 刺激试验的比较结果、17 - 酮类固醇的色谱分离以及卵巢静脉和肾上腺静脉中的血浆睾酮水平。对13例多毛症和男性化患者进行了如下研究:1. 在给予地塞米松(DXM)和绒毛膜促性腺激素(HCG)进行抑制 - 刺激试验期间,通过放射免疫测定法(RIA)测量血浆睾酮(T)水平。2. 对尿中17 - 酮类固醇、孕二醇(P2)和孕三醇(P3)进行色谱测定。试图根据1和2的结果将男性化分为“卵巢性”或“肾上腺性”。3. 通过股静脉进行双侧卵巢和肾上腺静脉插管以测量T(RIA)水平。4. 为治疗和活检目的进行双侧卵巢楔形切除术的剖腹手术。手术期间对卵巢静脉进行手术插管。这些测试结果表明:a)动态DXM - HCG试验可用于区分卵巢不参与T形成的病例和明显参与T形成的病例。b)尿类固醇的色谱测定没有病因学价值,因为不同组分的变化不显著。c)在所有患者中,T的主要来源是肾上腺而非卵巢,即使卵巢输出血管中的T有所增加。

相似文献

1
[Biological parameters of virilism in women].[女性男性化的生物学参数]
Ann Endocrinol (Paris). 1978;39(6):439-49.
2
Preoperative localization of a testosterone-secreting ovarian tumor by retrograde venous catheterization and selective sampling.
Am J Obstet Gynecol. 1974 Sep;120(1):91-6. doi: 10.1016/0002-9378(74)90184-7.
3
[Effect of wedge excision of the ovary on steroid excretion in virilism].
Zentralbl Gynakol. 1974 Jul 12;96(28):884-95.
4
Peripheral, ovarian, and adrenal vein steroids in hirsute women: acute effects of human chorionic gonadotropin and adrenocorticotrophic hormone.多毛女性外周血、卵巢及肾上腺静脉中的类固醇:人绒毛膜促性腺激素和促肾上腺皮质激素的急性效应
Fertil Steril. 1975 Sep;26(9):877-88.
5
Hirsutism and virilism in women.女性多毛症和男性化
Spec Top Endocrinol Metab. 1984;6:55-93.
6
Diagnostic evaluation of hirsutism in women by selective bilateral adrenal and ovarian venous catheterization.
Fertil Steril. 1978 Sep;30(3):283-8.
7
Selective venous catheterization in the evaluation of hyperandrogenism.在高雄激素血症评估中进行选择性静脉插管术。
J Endocrinol Invest. 1991 Dec;14(11):949-56. doi: 10.1007/BF03347121.
8
Diurnal change of serum androstenedione and testosterone and response to hCG and dexamethasone in women with polycystic ovaries, adrenal hyperandrogenism and unexplained hirsutism.多囊卵巢、肾上腺雄激素过多症及不明原因多毛症女性血清雄烯二酮和睾酮的昼夜变化以及对人绒毛膜促性腺激素和地塞米松的反应
Acta Endocrinol (Copenh). 1980 Feb;93(2):216-22. doi: 10.1530/acta.0.0930216.
9
[Suppression-stimulation functional test in virilism. Assay of a new method for determination of testosterone in plasma].[男性化的抑制-刺激功能试验。血浆睾酮测定新方法的分析]
Acta Ginecol (Madr). 1975 Jun 15;26(12):643-8.
10
Determination of the source(s) of androgen overproduction in hirsutism associated with polycystic ovary syndrome by simultaneous adrenal and ovarian venous catheterization. Comparison with the dexamethasone suppression test.通过同时进行肾上腺和卵巢静脉插管来确定多囊卵巢综合征相关多毛症中雄激素过度产生的来源。与地塞米松抑制试验的比较。
J Clin Endocrinol Metab. 1986 Nov;63(5):1204-10. doi: 10.1210/jcem-63-5-1204.