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International Journal of Clinical Obstetrics and Gynaecology

International Journal of Clinical Obstetrics and Gynaecology

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P-ISSN: 2522-6614, E-ISSN: 2522-6622
Peer Reviewed Journal

International Journal of Clinical Obstetrics and Gynaecology

2025, Vol. 9, Issue 2, Part C

Uterine didelphys: A rare case report of an incidental intraoperative diagnosis
Author(s): Mazen Mohammed Alrassad, Amr Ahmed Mahmoud, Taghreed Alnakeeb, Ahmed Mohamed Kamal Bakr and Amr Nabih Eisa
Abstract: Uterine didelphys is a rare congenital Müllerian anomaly characterized by the failure of fusion of the paramesonephric ducts, resulting in two separate uteri, often associated with variations in vaginal, cervical, and adnexal structures. This report presents an unusual case of a 34-year-old female with a history of two prior cesarean deliveries, who was admitted in labor at 7 cm cervical dilation. During an emergency cesarean section at Kafr Eldawar General Hospital, a second, previously undiagnosed uterus was discovered intraoperatively. This nongravid uterus was found to have a previous surgical scar, indicating a prior pregnancy, and had the right ovary and fallopian tube, whereas the gravid uterus lacked these structures. This case highlights the importance of considering Müllerian anomalies in obstetric patients, emphasizing the role of intraoperative vigilance and thorough surgical evaluation.
Pages: 163-166 | 180 Views | 87 Downloads
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International Journal of Clinical Obstetrics and Gynaecology
How to cite this article:
Mazen Mohammed Alrassad, Amr Ahmed Mahmoud, Taghreed Alnakeeb, Ahmed Mohamed Kamal Bakr, Amr Nabih Eisa. Uterine didelphys: A rare case report of an incidental intraoperative diagnosis. Int J Clin Obstet Gynaecol 2025;9(2):163-166. DOI: 10.33545/gynae.2025.v9.i2c.1610
International Journal of Clinical Obstetrics and Gynaecology

International Journal of Clinical Obstetrics and Gynaecology

International Journal of Clinical Obstetrics and Gynaecology