有学者将先天性阴道闭锁分为两型:Ⅰ型系阴道下段闭锁,其阴道上段及子宫正常;Ⅱ型系阴道完全闭锁,多合并宫颈发育不良,子宫体正常或畸形,子宫内膜可有正常分泌功能[1,2]。1984年3月至2009年3月我院收治29例先天性宫颈闭锁患者中,26例合并阴道完全闭锁,1例合并阴道上段闭锁,2例 Some scholars will be divided into two types of congenital vaginal atresia: type I vaginal atresia block, the upper vagina and the uterus normal; type Ⅱ Department of the vagina completely blocked, combined with cervical dysplasia, normal or abnormal uterus, the endometrium may have Normal secretory function [1,2]. March 1984 to March 2009 admitted to our hospital in 29 cases of congenital cervical atresia patients, 26 patients with vaginal complete closure, 1 case combined with vaginal upper block, 2 cases