先天性无阴道是双侧米勒发育不全的结果[1],根据国外资料,其发病率可以达到1/5000～1/4000,所以在临床上这类患者并不少见。先天性无阴道患者的治疗主要是创造一个解剖上和功能上接近正常状态的人工阴道,目前随着腹腔镜腹膜阴道成形术(罗湖一式及罗湖二式)[2-3]术式的成熟和改进,这种治疗方法变得简单易行。但在临床工作中,我们也发现有些此 Congenital absence of vagina is the result of bilateral Miller hypoplasia [1], according to foreign data, the incidence rate can reach 1/5000 ~ 1/4000, so in clinical patients with such is not uncommon. The treatment of congenital non-vaginal patients is to create an artificial vagina that is anatomically and functionally close to normal. Currently, with the development of laparoscopic peritoneal vaginoplasty (Luohu and Luohu II) [2-3] Improved, this treatment method becomes easy. But in the clinical work, we also found some of this