Uterine didelphys: a rare case report
DOI:
https://doi.org/10.18203/2320-1770.ijrcog20150760Keywords:
Uterus Didelphys, Mullerian Ducts, ProlapseAbstract
Uterus Didelphys is a rare congenital abnormality of uterus in which uterus is present as a paired organ when the embryogenetic fusion of the mullerian ducts fail to occur .As a result there occurs a double uterus with two separate cervices and often a double vagina as well. Each uterus has a single horn linked to the ipsilateral fallopian tube that faces its ovaries. We present a case of a multiparous lady who has uterus didelphys has previous two normal vaginal deliveries and during her third delivery she has prolapse of non-gravid uterus during second trimester which reduced gradually but spontaneously with advancing gestational age and she delivered a male child by caesarean section due to oligohydramnios with breech presentation during current pregnancy.
References
Grimbizis GF, Camus M, Tarlatzis BC, Bontis JN, Devroey P. “Clinical implications of uterine malformations and hysteroscopic treatment results”. Human Reproduction Update. 2001;7(2):161-74.
Carrington BM, Hricak H, Nuruddin RN, et al. Mullerian ducts anomalies: MR imaging evaluation. Radiology. 1990;176:715-20.
Cansole D, Tamburrini S, Barresi D, et al. The value of MR imaging in the evaluation of Mullerian ducts anomalies. Radiol Med. 2001;102:226-32.
Brown MA. MR imaging of benign uterine disease. Magn Reson Imaging Clin N Am. 2006;14:439-53.
Heinonen PK. “uterus diadelphys: a report of 26 cases” European journal of obstetrics & gynecology & reproductive biology. 1984;17(5):345-50.
Pui M. “Imaging diagnosis of congenital uterine malformation” Computerized medical imaging and graphics. 2004;28(7):425-33.