Wu R H, Boyar R M, Knight R, Hellman L, Finkelstein J W
J Clin Endocrinol Metab. 1976 Sep;43(3):506-11. doi: 10.1210/jcem-43-3-506.
An 18-year-old phenotypic girl with XY gonadal agenesis had endocrine studies. The patient had a small amount of sexual hair, a slightly enlarged clitoris, normal labia and no posterior fusion. Her vagina was of normal length, but no cervix was palpable. At laparoscopy, no gonads, uterus or fallopian tubes were identified. The buccal smear was chromatin negative and the karyotype was 46XY. The 24 h LH plasma pattern was qualitatively similar to that found in normal late pubertal subjects, but the values were in the castrate range. The 24h mean plasma concentrations of testosterone and dihydrotestosterone were 16.4 ng/dl and 14.2 ng/dl, respectively. Urinary estrogen excretion was 15 and 19 mug/day. These clinical and endocrine findings suggest that the patient was a genetic male in whom Mullerian regression occurred normally; however, the testes probably ceased functioning early in gestation preventing normal development of the Wolffian system. This set of events resulted in agenesis of the gonaductal system and female external genitalia. The patient represents the second example of this variation of male pseudohermaphroditism associated with XY gonadal agenesis.
一名患有XY性腺发育不全的18岁表型女性接受了内分泌检查。患者有少量阴毛,阴蒂略增大,阴唇正常且无后融合。她的阴道长度正常,但未触及宫颈。腹腔镜检查未发现性腺、子宫或输卵管。口腔涂片染色质阴性,核型为46XY。24小时促黄体生成素血浆模式在质量上与正常青春期晚期受试者相似,但数值处于去势范围内。睾酮和双氢睾酮的24小时平均血浆浓度分别为16.4 ng/dl和14.2 ng/dl。尿雌激素排泄量为每天15和19微克。这些临床和内分泌结果表明,该患者是一名遗传男性,其中苗勒氏管正常退化;然而,睾丸可能在妊娠早期停止功能,阻止了沃尔夫管系统的正常发育。这一系列事件导致性腺管系统发育不全和女性外生殖器。该患者是与XY性腺发育不全相关的男性假两性畸形这种变异的第二个例子。