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Impact of clinical, hormonal, radiological, and immunohistochemical studies on the diagnosis of postmenopausal hyperandrogenism

机译:临床,激素,放射学和免疫组化研究对绝经后高雄激素血症的诊断的影响

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摘要

Postmenopausal biochemical hyperandrogenism occurs rarely. The presence of an underlying tumor in women with this condition may be missed without careful evaluation.- Androgen excess in these women is the result of either tumoral or nontumoral causes. Factors that distinguish between tumoral and nontumoral etiology have not been identified.The primary goal of this retrospective study was to identify specific characteristics that could help differentiate between tumoral or nontumoral etiology among postmenopausal women suspected of having an androgen-secreting tumor. Participants were 22 postmenopausal women with biochemical hyperandrogenism referred to a medical center between 1995 and 2009. Clinical, biological, and morphological evaluations were performed in all women. Surgical resection of both ovaries was most often proposed for women without adrenal tumors, and immunocytochemical studies of the ovaries were performed.Among the 22 participants, 8 cases of ovarian tumors were identified based on ultrasound and/or magnetic resonance imaging. Two additional cases had an adrenal tumor diagnosed by computed tomography. The remaining 12 women had various nontumoral conditions. The clinical presentation in women with and without tumors was very similar. Some differences between the 2 groups, however, were found in the biological phenotype. Compared with women without tumors, women with tumors had significantly higher levels of testosterone [2.6 (2.7) vs 0.9 (0.9) ng/mL, P < 0.05] and lower levels of basal follicle-stimulating hormone [FSH; 26.5 (22.9) vs 66.5 (26.0) IU/L, P < 0.01] and luteinizing hormone [12.0 (8.6) vs 24.1 (8.9) IU/L, P < 0.05]. Based on the likelihood ratio, the risk of having a testosterone level of 1.4 ng/mL or greater or an FSH level of 35 IU/L or less in postmenopausal women with a tumor was 8.4 and 10.8 times higher, respectively. Immunochemistry using P450cl7alpha antibody allowed identification of an elevated number of ovarian androgen-producing cells in 5 patients with tumors undetectable by conventional histology.These findings show no differences in clinical phenotype that can be used to discriminate between androgen-secreting tumors and other nontumoral causes of postmenopausal hyperandrogenism. The data suggest that 2 hormonal phenotypes, testosterone and basal FSH levels, may be discriminating markers.
机译:绝经后生化高雄激素很少发生。如果不进行仔细评估,可能会漏掉患有这种疾病的女性中潜在的肿瘤。-这些女性中雄激素过多是由于肿瘤或非肿瘤原因引起的。尚无区分肿瘤和非肿瘤病因的因素。这项回顾性研究的主要目的是确定可有助于在怀疑患有雄激素分泌性肿瘤的绝经后妇女中区分肿瘤或非肿瘤病因的具体特征。参与者是1995年至2009年间转诊到医学中心的22位绝经后生化高雄激素血症女性。对所有女性均进行了临床,生物学和形态学评估。对于没有肾上腺肿瘤的女性,通常建议对两个卵巢进行手术切除,并对卵巢进行免疫细胞化学研究。在22名参与者中,根据超声和/或磁共振成像确定了8例卵巢肿瘤。另外两个病例通过计算机断层扫描诊断为肾上腺肿瘤。其余12名妇女患有各种非肿瘤性疾病。有或没有肿瘤的女性的临床表现非常相似。但是,在生物学表型上发现了两组之间的一些差异。与没有肿瘤的女性相比,患有肿瘤的女性的睾丸激素水平显着较高[2.6(2.7)vs 0.9(0.9)ng / mL,P <0.05],而基础卵泡刺激素水平较低[FSH; 26.5(22.9)vs 66.5(26.0)IU / L,P <0.01]和黄体生成激素[12.0(8.6)vs 24.1(8.9)IU / L,P <0.05]。根据可能性比,绝经后患有肿瘤的女性睾丸激素水平达到1.4 ng / mL或更高或FSH水平达到35 IU / L或更低的风险分别高8.4倍和10.8倍。使用P450cl7alpha抗体进行的免疫化学分析可以鉴定5例常规组织学无法检测到的肿瘤中卵巢雄激素产生细胞的数量增加,这些发现表明,临床表型没有差异,可用于区分分泌雄激素的肿瘤和其他非肿瘤原因绝经后高雄激素血症。数据表明,两种激素表型,睾丸激素和基础FSH水平可能是区分标记。

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