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一名患有多囊卵巢疾病的母亲所生新生儿的女性假两性畸形。

Female pseudohermaphroditism in a neonate born to a mother with polycystic ovarian disease.

作者信息

Bilowus M, Abbassi V, Gibbons M D

出版信息

J Urol. 1986 Nov;136(5):1098-100. doi: 10.1016/s0022-5347(17)45231-1.

Abstract

A newborn with female pseudohermaphroditism (profound masculinization of the external genitalia and preservation of the internal female genitalia) is presented. During pregnancy progressive hirsutism was noted in the mother, and polycystic ovaries were found at cesarean section. The serum testosterone level in the cord blood was elevated markedly (1,232 ng./dl). After birth the serum testosterone levels of the mother and newborn decreased dramatically. Over-all it appears that the polycystic ovaries were the source of the excessive androgen secretion that caused maternal and fetal masculinization during the pregnancy.

摘要

本文报告了一名患有女性假两性畸形(外生殖器严重男性化而内生殖器保留为女性)的新生儿。孕期母亲出现进行性多毛症,剖宫产时发现多囊卵巢。脐血中血清睾酮水平显著升高(1232 ng./dl)。出生后母亲和新生儿的血清睾酮水平急剧下降。总体来看,多囊卵巢是孕期导致母体和胎儿男性化的过量雄激素分泌的来源。

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