摘要
The most common presentation of congenital absence ofthe vagina is known as Mayer-Rokitansky-Kuster-Hauser(MRKH) syndrome.Several procedures, invasiveand noninvasive, have been used for the creation of aneovagina. A technique frequently used for this purposein China over the last 20 years is rectosigmoidcolpopoiesis. Here we report a successful rectosigmoidcolpopoiesis done laparoscopically in a patient withMRKH syndrome.