Nazer Ahmed, Abu-Zaid Ahmed, Alomar Osama, Salem Hany, Azzam Ayman, Al-Badawi Ismail A
Department of Obstetrics and Gynecology, King Faisal Specialist Hospital and Research Center (KFSH&RC), P.O. Box 3354, Riyadh 11211, Saudi Arabia.
Case Rep Obstet Gynecol. 2013;2013:450165. doi: 10.1155/2013/450165. Epub 2013 Oct 31.
Müllerian duct anomalies (MDAs) encompass a group of anatomical malformations resulting from defective development, fusion, migration, or resorption of Müllerian (paramesonephric) ducts during embryonic life. Herein, we report the first case of an exceedingly uncommon MDA (bilateral ectopic hypoplastic uteri attached to bilateral pelvic sidewalls) in a 21-year-old woman who was referred to our tertiary care center as a case of primary amenorrhea for workup and further management.
苗勒管异常(MDAs)包括一组由于胚胎期苗勒管(副中肾管)发育、融合、迁移或吸收缺陷而导致的解剖学畸形。在此,我们报告首例极其罕见的苗勒管异常病例(双侧异位发育不全子宫附着于双侧盆腔侧壁),该病例为一名21岁女性,因原发性闭经转诊至我们的三级医疗中心进行检查和进一步治疗。