多囊卵巢综合征现状1:定义、病理生理、临床表现、诊断及并发症

K. Zoltán, Kun Ildikó, Kolcsár Melinda
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摘要

摘要:多囊卵巢综合征(PCOS)是育龄妇女中最常见的内分泌疾病,是多毛症最著名的病因,假设患病率为8-22%。论文的第一部分讨论了该综合征的概念演变,从1935年Stein和Leventhal的描述到今天。它描述了标准体系的变化,强调2003年由欧洲人类生殖与胚胎学会/美国生殖医学学会提出的鹿特丹标准至今仍然有效。该系统与早前(1990年)的nih标准在一个方面基本不同:它引入了两种新的表型,一种没有高雄激素症,另一种有排卵周期,因此它区分了4种表型。多囊卵巢综合征的病因和发病机制是异质性的,多因素的,目前尚不清楚。我们提出了3种主要的假设(1 -下丘脑-垂体紊乱,2 -卵巢原发性酶紊乱,或卵巢/肾上腺类固醇生成,主要导致17 α -羟化酶/17,20-裂解酶亢进,3 -胰岛素抵抗-高胰岛素血症和其他代谢功能障碍)。我们强调基因决定的高雄激素症的作用,胰岛素抵抗-高胰岛素症和相互加强的重要性。随后,讨论了代谢综合征的加重方面,然后讨论了上述病理过程对参与性功能调节的内分泌和其他器官结构的影响。我们强调围产期和青春期雄激素暴露在多囊卵巢综合征发病机制中的假设作用。本文还讨论了排卵的机制和子宫内膜病变的机制。并对其临床表现、临床旁及实验室检查、阳性诊断及鉴别诊断及并发症作了介绍。我们打算在接下来的一篇论文中讨论多囊卵巢综合征的治疗方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current aspects of polycystic ovary syndrome I: definition, pathophysiology, clinical manifestations, diagnosis and complications
Abstract Polycystic ovary syndrome (PCOS) is the most frequent endocrine disease among women with childbearing potential, the best-known cause of hirsutism, with a hypothesized prevalence of 8-22%. The first part of the paper discusses the conceptional evolution of the syndrome, from its description in 1935 by Stein and Leventhal till today. It describes the changes in the criteria systems, emphasizing that the Rotterdam criteria, proposed in 2003 by the European Society for Human Reproduction and Embryology/American Society for Reproductive Medicine, are still valid today. This system basically differs from earlier (1990) NIH-criteria in one aspect: it introduced two newer phenotypes, one without hyperandrogenism and the other with ovulatory cycles, so it distinguishes 4 phenotypes. The etiology and pathogenesis of PCOS is heterogeneous, multifactorial, poorly understood. We present the 3 leading hypotheses (1 - hypothalamo-hypophyseal disturbances, 2 – primary enzyme disorders in ovarian, or ovarian/adrenal steroidogenesis, resulting primarily in hyperactivity of 17alpha-hydroxylase/17,20-lyase, 3 – insulin resistance-hyperinsulinism and other metabolic dysfunctions). We emphasize the role of genetically determined hyperandrogenism, that of insulin resistance-hyperinsulinism and the importance of reinforcing each other. Subsequently, the aggravating aspects of the frequently associated metabolic syndrome are discussed, and then the effects of the mentioned pathological processes on the endocrine and other organ structures participating in the regulation of sexual functions. We stress the hypothetical role of perinatal and pubertal androgen exposition in the pathogenesis of PCOS. The mechanisms of anovulation and those of the endometrial lesions are discussed, too. The clinical manifestations, the paraclinical and laboratory examinations, the positive and differential diagnosis and the complications are also presented. We intend to deal with the therapeutic aspects of PCOS in an upcoming paper.
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