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男性假两性畸形——睾丸女性化,又称睾丸女性化综合症,比较少见,我院1983年至1989年收治3例,现报告如下。临床资料3例社会性别均为女性,已婚,均因原发性闭经、不孕、双侧大阴唇部有肿块而就诊。均否认有家族史。女性体态,面容消瘦型,发育中等,智力正常。3例均无胡须、喉结,乳房发育差,乳头小,乳晕色浅。2例无腋毛、阴毛,妇科检查均未扪及宫颈、子宫、附件,见附表。
Male false bisexual deformity - Testicular feminization, also known as testicular feminization syndrome, is relatively rare, our hospital from 1983 to 1989 admitted to 3 cases, are as follows. Clinical data 3 cases of female gender, married, are due to primary amenorrhea, infertility, bilateral labia minora lumps and treatment. Both denied family history. Female body shape, face thin, moderately developed, normal intelligence. No beard in 3 cases, Adam’s apple, poor breast development, small nipple, and areola color. 2 cases without armpit hair, pubic hair, gynecological examination did not palpable cervix, uterus, annex, see Schedule.