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先天性无阴道是一种并不罕见的生殖器官异常性疾病,国外文献报道其发病率为1/4000～5000。临床上较多见于女性生殖道畸形综合症亦称Rokitansky—kuster—Hauset(R—K—H)综合征。我科曾采用羊膜移植法、植皮法、皮瓣法,效果均不理想。1986年12月我们采用乙状结肠代阴道成形术一例,效果满意,现报道如下。病历介绍患者女,22岁。住院号6470。主因青春期后无月经来潮,近一年自觉周期性下腹隐痛,不治自愈,结婚两个月性交困难,于1986年11月12日住院。
Congenital absence of the vagina is not uncommon genital abnormalities, foreign reports of its incidence of 1/4000 ~ 5000. More common in clinical female reproductive tract deformity syndrome also known as Rokitansky-kuster-Hauset (R-K-H) syndrome. My department had used amniotic membrane transplantation, skin grafting, flap method, the effect is not satisfactory. December 1986 we use sigmoid colon vaginoplasty a case of satisfactory results are reported below. Patient female medical record, 22 years old. Hospital number 6470. Mainly due to no menstrual cramps after puberty, spontaneous recurrent lower abdominal pain nearly a year, healed, married two months of sexual intercourse difficult, in November 12, 1986 hospitalization.