Robert’s Uterus: An Uncommon Presentation of Congenital Mullerian Duct Anomaly [PDF]
Gynecology and Minimally Invasive TherapyPandit Palaskar +3 more
doaj +5 more sources
Pregnancy in a blind hemi-cavity of Robert’s uterus with ipsilateral renal agenesis: a case report and literature review [PDF]
Journal of International Medical Research, 2019 Robert’s uterus is an asymmetric septate uterus with a noncommunicating cavity and is a rare Müllerian anomaly. We present a rare case of pregnancy in a blind cavity and the first report of ipsilateral renal agenesis.
Qiao-Mei Yang +4 more
doaj +2 more sources
Clinical and Experimental Obstetrics & Gynecology, 2021 Background: Robert’s uterus is a rare müllerian duct anomaly described as an asymmetric septate uterus with a noncommunicating cavity. Its main presentation is recurrent cyclical abdominal pain.
Ji-Chen Wang +4 more
doaj +2 more sources
Type II Robert's Uterus Presenting as Long‐Standing Secondary Subfertility: Diagnosis Confirmed by Combined Laparoscopy and Hysteroscopy in a Bangladeshi Patient [PDF]
Clinical Case ReportsRobert's uterus is a rare congenital Müllerian duct anomaly characterized by an asymmetric septum dividing the uterine cavity into a communicating and a blind hemicavity despite a normal external contour.
Iftekhar Ahmed Sakib +3 more
doaj +2 more sources
Journal of Pediatric Surgery Case ReportsIntroduction: Robert's uterus, with ipsilateral renal agenesis, is an exceptionally rare Mullerian duct anomaly (MDA). It usually presents with cyclical pain, but presentation as pelvic inflammatory disease in an adolescent is extremely uncommon.
Akkamahadevi C. Hiremath +3 more
doaj +2 more sources
Diagnosis and treatment of Robert’s uterus combined with transverse uterine septum: a case report and review of the literature [PDF]
Frontiers in MedicineBackgroundRobert’s uterus combined with transverse uterine septum is a rare uterine malformation. Only one case has been reported to date, and it is challenging to diagnose and treat.Case presentationHere we report the case of a 19-year-old female had ...
Mingqian Chen +5 more
doaj +2 more sources
Robert's uterus (asymmetric septate uterus): a rare congenital Müllerian duct anomaly. [PDF]
BMJ Case Rep, 2022 Müllerian anomalies such as Robert’s uterus, which was first described by the French gynaecologist Dr Helene Robert in 1969, are rare clinical entities and have been reported in <3% of the female population. Robert’s uterus is a rare phenomenon with a relative dearth of reported cases.
Dunphy L +4 more
europepmc +4 more sources
Minimally invasive surgical treatment of Robert’s uterus with missed miscarriage: case report
Journal of Obstetrics and GynaecologyRobert’s uterus was firstly reported in 1970, it’s a rare Müllerian duct anomaly with 2 intra-uterine cavities divided by asymmetrical septum. One of the cavities is completely obstructed to cervix by septum and menstruation fluid retents in this blind ...
Houyu Yang, Yuanjunzi Shi, Gang Ji
doaj +3 more sources
Hysteroscopic Management of Robert's Uterus. [PDF]
J Obstet Gynaecol India, 2020 Shah N, Changede P.
europepmc +4 more sources
Magnetic Resonance Imaging (MRI) Depiction of Robert's Uterus: A Rare Müllerian Duct Anomaly Presenting with Cyclical Pain in Young Menstruating Woman. [PDF]
Pol J Radiol, 2017 BACKGROUND: Robert's uterus is a very rare müllerian duct anomaly which is characterised by septate uterus with obstruction of a one-sided cavity and formation of hematometra.
Mittal P +5 more
europepmc +2 more sources