Case Report
Volume 7 Issue 8 - 2018
Magnetic Resonance Imaging and Ultrasound Depiction of Robert’s Uterus: A Rare Müllerian Duct Anomaly Causing Left Hematometra and Left Hematosalpinx
Nehal Mohamed Ibrahim Saloum1, Mohamed Mohamed Helmi Ahmed1*, Amal Mohamed Hassan Alobaidli1 and Ahmed Emad Taha Mahfouz2
1Department of Clinical Imaging, Women’s Wellness Research Center, Hamad Medical Corporation, Doha, Qatar
2Department of Clinical Imaging, Hamad General Hospital, Hamad Medical Corporation, Doha, Qatar
*Corresponding Author: Mohamed Mohamed Helmi Ahmed, Department of Clinical Imaging, Women’s Wellness Research Center, Hamad Medical Corporation, Doha, Qatar.
Received: July 24, 2018; Published: August 07, 2018
Citation: Mohamed Mohamed Helmi Ahmed., et al. “Magnetic Resonance Imaging and Ultrasound Depiction of Robert’s Uterus: A Rare Müllerian Duct Anomaly Causing Left Hematometra and Left Hematosalpinx”. EC Gynaecology 7.8 (2018): 328-332.
Abstract
Robert’s uterus is a rare unique mullerian duct anomaly, first reported by Robert in 1970. The uterus shows two uterine cavities with one is being blind causing hematometra and the other cavity is communicating to a single cervix. So the patients present with cyclic abdominal pain during menstruation in spite of normal menstrual flow.
Any associated hematometra or endometriomas complicating this condition can be depicted with MRI which aid in the appropriate management.
We present magnetic resonance imaging (MRI) and ultrasound findings in a case of Robert’s uterus in 16 years old young woman.
Keywords: Dysmenorrhea; Hematometra; Mullerian Duct Anomaly; Robert’s Uterus; Septate Uterus
Copyright: © 2018 Mohamed Mohamed Helmi Ahmed., et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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