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继发于17β-羟类固醇脱氢酶缺乏的男性假两性畸形:青春期的性别角色转变

Male pseudohermaphroditism secondary to 17 beta-hydroxysteroid dehydrogenase deficiency: gender role change with puberty.

作者信息

Imperato-McGinley J, Peterson R E, Stoller R, Goodwin W E

出版信息

J Clin Endocrinol Metab. 1979 Sep;49(3):391-5. doi: 10.1210/jcem-49-3-391.

Abstract

A 31-yr-old male pseudohermaphrodite is reported with 17 beta-hydroxysteroid dehydrogenase deficiency. Laboratory data revealed a plasma testosterone of 228 ng/100 ml, a plasma androstenedione of 620 ng/100 ml, and an abnormal androstenedione to testosterone ratio. Plasma estradiol was 4.6 ng/100 ml and plasma estrone was 22 ng/100 ml. This subject was born in a hospital, incontrovertibly declared to be a female, and unambiguously raised as a girl by his parents for the first 17 yr of his life. At age 14 yr, he was able to change to a male gender role with ease. As an adult, he is a well adjusted, happily married man with a successful professional career. Surgical correction of bilateral cryptorchidism and hypospadias was carried out at age 14 yr. At age 30 yr, he developed a teratocarcinoma-seminoma of the right testis with retroperitoneal node metastases. After orchiectomy and retroperitoneal node dissection, he was placed on chemotherapy and is presently free of metastases.

摘要

报道了一名31岁男性假两性畸形患者,其患有17β-羟类固醇脱氢酶缺乏症。实验室数据显示,血浆睾酮为228 ng/100 ml,血浆雄烯二酮为620 ng/100 ml,且雄烯二酮与睾酮的比值异常。血浆雌二醇为4.6 ng/100 ml,血浆雌酮为22 ng/100 ml。该患者出生于一家医院,无可争议地被宣布为女性,并在其生命的前17年被父母明确当作女孩抚养。14岁时,他能够轻松转变为男性性别角色。成年后,他是一个适应良好、婚姻幸福的男子,拥有成功的职业生涯。14岁时进行了双侧隐睾和尿道下裂的手术矫正。30岁时,他患上了右侧睾丸畸胎癌-精原细胞瘤并伴有腹膜后淋巴结转移。在睾丸切除和腹膜后淋巴结清扫术后,他接受了化疗,目前无转移。

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