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假两性畸形在临床上比较少见,而且分类繁多,睾丸女性化综合征属罕见,国内文献报告者不多,我省更少,现报告一例。 病例报告: 患者张×× 住院号55597 21岁 已婚 回族 农民 主诉:婚后二月不能行正常之性生活而入院。患者的腹股沟有枣仁大的肿物,不痛不痒,随年龄而增大,习已为常,未曾注意,家人以女性抚养。20岁结婚,对方发现其无阴道,故用剪刀将其阴道口剪开,此后遗水不止。
Fake bisexual deformities are relatively rare in clinical practice, and the classification of many, testicular feminization syndrome is rare, few domestic literature reports, less in our province, the report is a case. Case Report: Zhang × × Hospital No. 55597 21-year-old married Muslim farmers complained: February marriage can not be normal sexual life and admission. Patients with groin Zao Ren large tumor, itching, with age and increase, habitual has been, did not notice, the family reared with women. 20-year-old married, the other found no vaginal, it cut its vaginal opening with scissors, after leaving more than water.