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男性两性畸形睾丸女性化综合症,近年来有少数报导。现将我院收治一例报告如下: 患者王××,社会性别女性,6岁,于1985年12月19日以右侧腹股沟斜疝收住院。既往无肝炎、结核病史,曾接种过各种疫苗,本人为足月顺产所生,在胎儿期前6个月,其母亲曾服用避孕药(药名不洋),后发现已怀孕6个月时停药。父母非近亲结婚,家族中及患儿两姐姐无同病史。检查:T36℃,R21次/分,P120次/分,BP80/50mm H。女性外貌,发育正常,营养中等,五官端正,喉结平坦,乳头发育正常,心肺腹无异常,右侧腹股沟处可触及活动性4×3cm肿物,呈椭园形.质地软,可还纳。
Male genital abnormalities testicular feminization syndrome, a few reported in recent years. Now admitted to our hospital a case report is as follows: Patient Wang × ×, female gender, 6 years old, on December 19, 1985 to the right inguinal hernia admitted to hospital. Past no history of hepatitis, tuberculosis, had vaccinated a variety of vaccines, I gave birth to term full-term, 6 months before the fetus, the mother had contraceptives (drug name is not foreign), was found to be 6 months pregnant When the withdrawal. Parents of non-relatives married, family and children with no history of the two sisters. Check: T36 ℃, R21 beats / min, P120 beats / min, BP80 / 50mm H. Female appearance, normal development, moderate nutrition, facial features, flat Adam’s apple, normal nipple development, no abnormal heart and lung abdomen, the right groin can reach the activity of 4 × 3cm tumor, was oval-shaped. Soft texture can be satisfied.