女性假两性畸形在临床上非常罕见，我院于1997年收治1例，报告如下。患者，女。7岁。因外阴畸形7年，于1997年3月8日入院。患者出生时，即表现阴蒂较正常大，随着生长发育，患者阴蒂逐渐增大，至入院时为止，明带增大似小儿阴茎。患者4岁时出现阴毛，面部及周县皮肤出现痤疮， Female pseudohermaphroditism is clinically very rare, our hospital was admitted in 1997, 1 case, the report is as follows. Patients, women. 7-year old. Due to genital malformations for 7 years, in March 8, 1997 admission. Patients at birth, the performance of the clitoris than normal large, with the growth and development, the patient’s clitoris gradually increased, until admission, Ming band increased pediatric penis. At age 4, the patient developed pubic hair, acne on the face and Zhou County skin,