Objective: To report a rare uterine anomaly consisting of a normal uterus, a double cervix, and a double vagina.
Design: Case report.
Setting: University hospital.
Patient(s): A 28-year-old nulligravida patient referred for evaluation of primary infertility and a suspected müllerian anomaly.
Intervention(s): Clinical and surgical evaluation of the anomaly.
Main outcome measure(s): Description and treatment for a rare uterine anomaly and a subsequent literature search.
Result(s): Successful resection of vaginal septum and subsequent pregnancy.
Conclusion(s): This extremely rare anomaly is not explained by classic embryologic teachings, and it does not fit into the classification system currently used to describe müllerian anomalies.