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先天性子宫阴道缺如(MRKH)综合征是由于双侧副中肾管未发育或其尾端发育停滞而未向下延伸所致,表现为子宫及阴道发育不全,其发病率约为1/4500[1]。此类患者的核型为46XX,其智力及体格发育正常,卵巢发育及功能正常,具有典型的女性第二性征和性心理,所以有迫切的治疗要求。MRKH综合征的主要治疗方式为人工阴道成形术。我院采用悬吊式腹腔镜下的腹膜代阴道成形术治疗
Congenital uterine absence of the vagina (MRKH) syndrome is due to the development of bilateral unilateral middle or proximal tubal growth retardation and did not extend downward, manifested as uterine and vaginal hypoplasia, the incidence rate of about 1 / 4500 [1]. The karyotype of these patients is 46XX, with normal intelligence and physical development, normal ovarian development and function, typical female secondary sexual characteristics and psychology, so there is an urgent therapeutic requirement. The main treatment for MRKH syndrome is artificial vaginoplasty. In our hospital, the laparoscopic peritoneal vaginoplasty was performed