Bryner J R, Asch R H, Greenblatt R B
Obstet Gynecol. 1977 Jul;50(1 Suppl):30s-34s.
A report of a patient with bilateral gonadoblastomas who sought consultation for primary amenorrhea and infertility is presented. Thelarche and adrenarche occurred spontaneously at age 13. Clitoromegaly and a hypoplastic uterus were noted on physical examination. Flat plate X-ray of the abdomen demonstrated radiopaque material in both adnexa. Urinary 17-ketosteroid levels were normal, but the serum testosterone concentration was elevated. Serum gonadotropin values were markedly elevated, and total serum estrogens levels were very low. The karyotype was XY. The gonads were extirpated, and typical histology is demonstrated. A postulate was made to explain the clinical findings.
本文报告了一名患有双侧性腺母细胞瘤的患者,该患者因原发性闭经和不孕前来咨询。乳房发育和肾上腺功能初现于13岁时自发出现。体格检查发现阴蒂肥大和子宫发育不全。腹部平片显示双侧附件有不透X线的物质。尿17-酮类固醇水平正常,但血清睾酮浓度升高。血清促性腺激素值显著升高,血清总雌激素水平非常低。核型为XY。切除性腺,并展示了典型的组织学特征。提出了一个假说来解释临床发现。