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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1/4,000～5,000。临床上较多见于Rokitansky-Kuster-Hauser综合征者,少数为睾丸女性化综合征患者,极少数为真两性畸形及性腺发育不全病例。对于这种疾病的治疗首次作出尝试的是德国的Dupuytren,他于1817年对1例无阴道患者采用三棱套针在会阴处戳刺,但结果失败。嗣后,许多妇、外科学者相继设计了各种疗法并逐步进行了改进。疗法可分为非手术与手术两大类。手术疗法一种是在无阴道患者外阴部作一切口,并在尿道、膀胱和直肠间分
Congenital absence of the vagina is not uncommon genital abnormalities, foreign reports of the incidence of 1 / 4,000 to 5,000. Clinically more common in Rokitansky-Kuster-Hauser syndrome, a small number of testicular feminization syndrome patients, very few cases of true hermaphroditism and gonadal dysgenesis. The first attempt at treatment for the disease was in Germany, Dupuytren, who punctuated the perineum with a three-pronged trocar in 1817 without vaginosis, but failed. Subsequently, many women and surgeons successively designed various therapies and gradually improved them. Therapy can be divided into two categories of non-surgical and surgical. Surgical treatment is a non-vaginal patients in the vulva for a cut, and in the urethra, bladder and rectum