Results 61 to 70 of about 516 (142)

Diagnosis and gestational follow-up in a patient with Herlyn-Werner-Wünderlich syndrome, a case report

Taiwanese Journal of Obstetrics & Gynecology, 2019
Objective: Herlyn-Werner-Wünderlich syndrome (HWW) is a rare congenital malformation of the urogenital tract due to a fusion failure in the Müllerian ducts.
Laura Baños Cándenas, Daniel Abehsera Davó, Marta de la Peña Rodríguez de Medina, Jessica Martín Orlando, Andrés Carlos López Díaz   +4 more
doaj   +1 more source

Complex Presentation of Uterus Didelphys With Bilateral Leiomyomas: A Case Report

Case Reports in Obstetrics and Gynecology, Volume 2025, Issue 1, 2025.
Müllerian duct anomalies and uterine leiomyomas represent distinctive facets of female reproductive health. While uterine leiomyomas are prevalent reproductive pathologies, the coexistence of Müllerian anomalies and leiomyomas is relatively uncommon. This case study examines the complex medical and surgical management of a woman who initially presented
Assaye Mezgebu Wube, Yusuf Mohammed Yusuf, Biniyam Afework Abate, Meksud Shemsu Hussen, Yabets Tesfaye Kebede, Bekri Delil Mohammed, Manvinder Singh   +6 more
wiley   +1 more source

Uterus didelphys with obstructed hemivagina and renal agenesis : mri findings

Journal of the Belgian Society of Radiology, 2011
Müllerian duct abnormalities (MDA) are developmental disorders leading to dysmorphism of the female genital tract. Currently the Buttram and Gibbons classification of these entities is widely used. We present a case of a young girl with uterus didelphys and ipsilateral renal agenesis.
Yazdi, Amir, De Smet, Kristof, Caroline, Ernst, Desprechins, B., Johan, De Mey   +4 more
openaire   +6 more sources

Long‐term effects of surgically corrected menstrual outflow obstruction: A case–control study

International Journal of Gynecology &Obstetrics, Volume 165, Issue 1, Page 117-124, April 2024.
Abstract Objective To enhance evidence‐based knowledge on long‐term sequalae in patients with surgically corrected obstructing Müllerian anomalies. Methods This long‐term case–control study included patients with menstrual outflow obstruction due to congenital anomalies of the uterus or vagina, who were at least 18 years old, and for whom 2 years had ...
Lisanne Martens, Marian A. Spath, Monique A. van Beek, Wim N. P. Willemsen, Kirsten B. Kluivers   +4 more
wiley   +1 more source

Vaginoscopic resection of hemivagina, in a 20‐year‐old virgin female with prior misdiagnosis of OHVIRA syndrome as a bicornuate uterus: A case report

Clinical Case Reports, Volume 12, Issue 3, March 2024.
Key Clinical Message OHVIRA syndrome can be misdiagnosed due to its rarity, resulting in the need for more invasive interventions than vaginoscopy. Also, delayed diagnosis of OHVIRA syndrome can affect patient's quality of life by leading to chronic gynecological diseases such as endometriosis and pelvic inflammatory disease.
Ameneh Haghgoo, Ali Faegh, Saeed Nasiri, Farnaz Akhbari   +3 more
wiley   +1 more source

A rare case of symptomatic hydrometrocolpos in a 5y old female

Urology Case Reports, 2021
Late presentation of symptomatic hydrometrocolpos is uncommon. We present a 5 years old continent girl with prenatally diagnosed multicystic dysplastic left kidney and late-onset of lower abdominal pain.
Hussam Nassar, Maya Horst, Rita Gobet
doaj   +1 more source

Hysterosalpingography and Ultrasonography Features of Herlyn‐Werner‐Wunderlich Syndrome Detected during Infertility Workup

Case Reports in Radiology, Volume 2024, Issue 1, 2024.
The Herlyn‐Werner‐Wunderlich syndrome (HWWS) is a very rare congenital anomaly of the urogenital tract. It is characterized by a combination of didelphys uterus, unilateral vaginal obstruction, and ipsilateral renal agenesis. MRI imaging is usually used for diagnosis; however, the authors present a case of HWWS diagnosed by ultrasonography (HSG) and ...
Hidayatullah Hamidi, Bibi Hosai Balkhi, Atsushi Komemushi   +2 more
wiley   +1 more source

Uterus didelphys with imperforate hemivagina and ipsilateral renal agenesis complicated by hematocolpos, hematometra and hematosalpinex. The challenge of intact hymen

Middle East Fertility Society Journal, 2011
Background: Uterine didelphys with obstructed hemivagina is an extremely rare condition. This diagnosis should be considered whenever an adolescent is presented with severe dysmenorrhea and progressive pelvic mass. Case: A 15-year-old girl presented with
Kamal M. Zahran, Diaa Eldeen M. Abd El Aal, Moustafa H.M. Othman, Eman R. Ahmed   +3 more
doaj   +1 more source

Uterine didelphus with obstructed hemivagina.

Saudi medical journal, 2008
Complex congenital anomalies of the mullerian ducts can occur in isolation or in association with other developmental disorders. They result from non-development or non-fusion of the mullerian ducts or the failure of reabsorption of the uterine septum.
Malak M, Al-Hakeem, Samir A, Ghourab, Mohammed R, Gohar, Tariq Y, Khashoggi   +3 more
openaire   +1 more source

Uterus didelphys with obstructed hemivagina and ipsilateral renal anomaly syndrome: A rare cause of cyclic abdominal pain in a young female

International Journal of Advanced Medical and Health Research, 2016
Obstructed hemivagina and ipsilateral renal anomaly syndrome is a rare group of urogenital anomalies in which unilateral genital anomaly is associated with ipsilateral renal anomaly.
Kapish Mittal, Sharad Gupta, Puneet Mittal, Amit Mittal, Ranjana Gupta, Deepika Rao   +5 more
doaj   +1 more source