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睾丸女性化综合征是一种男性假两性畸形。1817年 Siegleher 首次报告1例,此后各作者所用名称不一,1953年 Morris 提出了“睾丸女性化”一词后,沿用至今。近年证明此综合征患者体内缺乏雄激素受体,又称对雄激素不敏感综合征。此类患者呈家族性遗传倾向,现将我科诊治的2例报告如下。例1 王×,18岁,社会性别女,住院号A39227。1986年7月因自幼运动后腹股沟出现包块来院就诊。外貌女性,身高162cm,体重45kg。喉结不凸起,女性声调。月经未来潮。乳房女性发育,乳晕
Testicular feminization syndrome is a male pseudohermaphroditism. In 1817, Siegleher first reported 1 case and the names used by different authors were different. After Morris proposed the term “feminization of testicles” in 1953, it has been used to date. In recent years, this syndrome shows that the lack of androgen receptor in vivo, also known as androgen insensitivity syndrome. These patients were familial genetic predisposition, now my treatment of 2 cases are reported below. Example 1 Wang ×, 18 years old, female gender, hospital number A39227. In 1986 July due to groin after childbirth appeared mass hospital for treatment. Female appearance, height 162cm, weight 45kg. Adam’s apple is not raised, female tone. Menstruation future tide. Breast female development, areola