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在女性生殖道畸形中,双子宫、双宫颈、双阴道畸形较为少见,合并单侧阴道盲端一侧肾输尿管缺如更为罕见。我院自1977年元月至1981年12月,五年共收治生殖道畸形25例,占妇科总住院人数的0.41％,其中子宫畸形9例,占生殖道畸形者的36％,合并妊娠3例,不合并妊娠6例。在9例子宫畸形中,双子宫、双宫颈、双阴道5例,其中合并单侧阴道盲端者4例,占子宫畸形的44％,此4例均有一侧肾输尿管缺如,其中左侧肾输尿管全缺2例,右侧肾输尿管全缺2例。现将此4例报道如下:
In female genital tract deformity, double uterus, double cervix, double vaginal deformity is relatively rare, combined with unilateral vaginal blind side renal ureter absent even more rare. Our hospital from January 1977 to December 1981, five years treated a total of 25 cases of genital malformations, accounting for 0.41% of total gynecological hospital, including 9 cases of uterine malformations, accounting for 36% of genital abnormalities, combined with pregnancy 3 Cases, 6 cases without pregnancy. In 9 cases of uterine malformations, double uterus, double cervix and double vagina in 5 cases, including unilateral vaginal blind end in 4 cases, accounting for 44% of uterine malformations, all of these 4 cases have kidney ureter absent, of which the left Nephrotic total absence of 2 cases, right kidney ureter missing in 2 cases. Now these 4 cases are reported as follows: