Abstract
Uterine didelphys is a congenital malformation characterized by the presence of two separated hemiuteri and hemivaginas, due to lack of midfusion of the Mullerian ducts. We report a case of UD-BHRA(uterine didelphys with blind hemivagina and ipsilateral renal agenesis), a rare type of uterine didelphys charaterized by symptomatic unilateral hematocolpos due to blind hemivagina after menarche and ipsilateral renal agenesis. The MRI findings in 22-year-old woman with bilateral ovarian tumors demonstrated two separated uterine horns and cervical and vaginal canals, with left hematocolpos and left renal agenesis.
REFERENCES
1.The American Fertility Society. The American Fertility Society classification of adnexal lesions, distal tubal occlusion, tubal occlusion, tubal occlusion secondary to tubal ligation, tubal pregnancies, mullerian anomalies, and intrauterine adhesion. Fertil Steril. 1988. 49:944–955.
2.Woolf RB., Allen WM. Concomitant malformations. The frequent simultaneous occurence of congenital malformations of the reproductive and urinary tracts. Obstet Gynecol. 1953. 2:236–265.
3.Anderson KA., McAninch JW. Uterus didelphia with left hematocolpos and ipsilateral renal agenesis. J Urol. 1982. 127:550–553.
4.Sardanelli F., Renzetti P., Oddone M., To ma P. Uterus Didelphys with blind hemivagina and ipsilateral renal agenesis: MR findings before and after vaginal septum resection. Eur J Radiol. 1995. 19:164–170.
5.Stassart JP., Nagel TC., Prem KA., Phipps WR. Uterus didelphys, obstructed hemivagina and ipsilateral renal agensis: the university of Minnesota experience. Fertil Steril. 1992. 57:756–761.
6.Woods Μ J., Sheppard RG., Hardman DA., Woods HJ. Congenital genitourinary anomalies. Is there a prediction for multiple primary malignant neoplasms? Cancer. 1992. 69:546–549.