Surgical management of an obstructive Müllerian Anomaly in a patient with anorectal malformation

Müllerian duct anomalies are rare in the general population, occurring less than 3% of women, but much more prevalent female patients with anorectal malformation, up to 30% these patients. Unicornuate uterus a rudimentary non-communicating horn is congenital anomaly development which can be seen isolation or conjunction other anomalies, several case reports described VACTERL association. These may asymptomatic until patient develops dysmenorrhea devastating obstetrical complications. We describe successful surgical management an obstructive post-pubertal malformation.