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卵巢巨大水肿与男性化。

Massive edema of the ovary and virilization.

作者信息

Vasquez S B, Sotos J F, Kim M H

出版信息

Obstet Gynecol. 1982 Jun;59(6 Suppl):95S-9S.

PMID:6283445
Abstract

Endocrine studies of a virilized adolescent patient with massive ovarian edema are reported. The histologic features of the affected ovary consisted of diffuse edematous stroma with scattered islands of lutein-like cells and no evidence of recent ovulation. Plasma concentrations of progesterone and 17-hydroxyprogesterone (17-OHP) in the peripheral and left ovarian veins and their ovarian-peripheral vein gradients were above the range observed during normal follicular phase. The considerable increase in the ovarian vein concentrations of both steroids observed after adrenocorticotropic hormone administration was noteworthy as a direct effect of this hormone on the ovarian synthesis of steroids has not previously been observed. Peripheral vein levels of testosterone (T) were increased. The secretion of T by the ovary was demonstrated by its elevated levels in the ovarian vein and in the ovarian-peripheral vein gradient. Unexpectedly, the levels of androstenedione in the ovarian vein were normal, suggesting an alteration in the ovarian biosynthetic pathway for the production of T. Similar findings have been observed in hirsute women with hyperthecosis ovarii. After surgery, the peripheral vein levels of 17-OHP and T returned to normal, pointing toward the ovary as their source of excess. The data indicate that stromal luteinization of the massive ovarian edema may lead to changes in normal ovarian steroidogenesis that would be responsible for the clinical manifestations of this disorder.

摘要

本文报道了一名患有大量卵巢水肿的男性化青春期患者的内分泌研究情况。患侧卵巢的组织学特征为弥漫性水肿性间质,伴有散在的黄体样细胞岛,且无近期排卵迹象。外周血及左侧卵巢静脉中孕酮和17-羟孕酮(17-OHP)的血浆浓度及其卵巢-外周静脉梯度均高于正常卵泡期所观察到的范围。值得注意的是,给予促肾上腺皮质激素后,观察到两种类固醇在卵巢静脉中的浓度显著增加,因为此前尚未观察到该激素对卵巢类固醇合成有直接作用。外周静脉睾酮(T)水平升高。卵巢静脉中T水平及其卵巢-外周静脉梯度升高,证明卵巢分泌T。出乎意料的是,卵巢静脉中雄烯二酮水平正常,提示卵巢产生T的生物合成途径发生改变。在患有卵巢泡膜细胞增生症的多毛女性中也观察到了类似的发现。手术后,外周静脉中17-OHP和T水平恢复正常,表明卵巢是其过量分泌的来源。数据表明,大量卵巢水肿的间质黄体化可能导致正常卵巢类固醇生成发生变化,这可能是该疾病临床表现的原因。

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