Neovagina Using Omental Flap in Patient with Mullerian Aplasia

Background: Vaginal agenesis is characterized by the absence or hypoplasia of the uterus, proximal vagina and the fallopian tubes. This anomaly has been recently termed müllerian aplasia by the American College of Obstetricians and Gynecologist. Müllerian aplasia is an uncommon, but not rare, anomaly. The estimated incidence is 1 in 5000 newborn females. Case: A 25 years old divorced female presents with history of primary amenorrhea. She was diagnosed prior to getting married with absence of the vagina along with the right kidney as case of Mayer– Rokitansky-Kuster-Hauser syndrome. The patient had a neovagina by omental flap. After six months of follow up she did well with an excellent anatomical outcome. [Abdulrahim Gari; Bandr Hafidh Adnan Gelidan; Salah Kary and Hussein T. Sabban. Neovagina Using Omental Flap in Patient with Mullerian Aplasia. J Am Sci 2012;8(6):204-207]. (ISSN: 1545-1003). http://www.americanscience.org. 25