Results 81 to 90 of about 2,413 (204)

Ultrasound‐guided cyst aspiration for management of acute adnexal torsion

Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 6, Page 790-797, June 2025.
ABSTRACT Objective Ultrasound‐guided cyst aspiration is a potential treatment for acute adnexal torsion that can be performed in the outpatient setting, offering an alternative to emergency laparoscopic surgery. The objective of this study was to describe our initial experience with aspiration of acutely torted adnexal cysts.
L. Berg, N. Eagles, S. Kastora, J. Farren, J. Naftalin, D. Jurkovic   +5 more
wiley   +1 more source

Notes on Marsupialian anatomy II. on the female genital organs of a virgin sarcophilus satanicus. [PDF]

, 1911
In a former communication to the Linnean Society of N.S.W. I described the genital apparatus in a female specimen of Sarcophilus satanicus which had borne young, and in that paper drew attention to various phenomena, especially in connection with the
Flynn, Theodore Thomson
core  

An incidental case of uterus didelphys and fibroids: Right sided myomectomy and left hemi-hysterectomy [PDF]

, 2020
Congenital anomalies of the uterus occur due to agenesis or lack of fusion of the Mullerian ducts. The incidence of these anomalies is largely  unknown since they are unlikely to be diagnosed in asymptomatic women. Uterine didelphys or double uterus
Chemwey , R., Kihara , A., Mashala, J.N., Pulei , A., Wekesa , D.   +4 more
core   +2 more sources

Clinical utility of ultrasonography in pediatric and adolescent gynecology: retrospective review of 1313 ultrasound examinations

Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 2, Page 226-234, February 2025.
ABSTRACT Objectives Ultrasound is the first‐line imaging modality of the pelvis in the pediatric and adolescent gynecology (PAG) population. Ultrasound findings in pre‐ and postpubertal PAG patients differ from those in adults. Diagnostic models for adnexal pathology have not been validated in this cohort.
N. Cooper, H. Meehan, K. Linton‐Reid, J. Barcroft, J. Danin, M. Seah, S. Sadigh, N. Bharwani, S. Sur, C. Fotopoulou, C. Landolfo, J. Yazbek, S. Saso, D. Timmerman, T. Bourne, M. Al‐Memar   +15 more
wiley   +1 more source

Late presentation, MR imaging features and surgical treatment of Herlyn-Werner-Wunderlich syndrome (classification 2.2); a case report

BMC Women's Health, 2018
Background Herlyn-Werner-Wunderlich syndrome is a very rare congenital genitourinary anomaly characterized by uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Case presentation Authors present a case of Herlyn-Werner-Wunderlich syndrome
Hidayatullah Hamidi, Nilab Haidary
doaj   +1 more source

Patients with anorectal malformation and upper limb anomalies:genetic evaluation is warranted [PDF]

, 2015
The objective of this study was to compare the prevalence of genetic disorders in anorectal malformation (ARM) patients with upper limb anomalies to that in ARM patients with other associated anomalies. A retrospective case study was performed in two
Bever, Y. (Yolande) van, Blaauw, I. (Ivo) de, Hondel, D. (Desiree) van den, IJsselstijn, H. (Hanneke), Klein, J.E.M.M. (Annelies) de, Marcelis, C.L.M. (Carlo), Sloots, C.E.J. (Pim), Wijers, C.H.W. (Charlotte)   +7 more
core   +1 more source

Uterus transplantation: A clinical breakthrough after systematic preclinical research

Reproductive Medicine and Biology, Volume 24, Issue 1, January/December 2025.
Abstract Background Uterus transplantation is a groundbreaking solution for absolute uterine factor infertility, offering women the potential for full biological motherhood. Since the first human trial in 2012 and the birth of the first baby in 2014, over 140 procedures have been performed globally, resulting in more than 70 live births.
Mats Brännström, Milan Milenkovic, Elias Tsakos   +2 more
wiley   +1 more source

Delayed Diagnosis of Uterus Didelphys Unicolis with Cervical Atresia in a Forty-Three-Year Old Unmarried Woman with Primary Amenorrhea

Gynecology Obstetrics & Reproductive Medicine, 2006
Müllerian duct fusion deficiency leads to uterus didelphys. We report the first case of a didelphysunicolis uterus with atretic cervix in a 43-y ear-old unmarried woman with a thirty years history of cyclic lower abdominal pain and primary amenhorrea. On
Ahmet Kale, Ahmet Yalınkaya, Nurten Akdeniz   +2 more
doaj  

The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review

Reproductive Medicine and Biology, Volume 24, Issue 1, January/December 2025.
ABSTRACT Background Müllerian duct anomalies (MDAs) are developmental malformations of the female genital tract that present as a series of abnormalities within the reproductive tracts of females. The etiology of MDAs is complex and heterogeneous, especially genetic factors.
Lin He, Shuya Chen, Yujun Sun, Zhi Zheng, Yuxiao Li, Chunfang Chu, Lin Li   +6 more
wiley   +1 more source

Spontaneous pregnancy at term with uterus didelphys: a case report [PDF]

, 2018
The uterus didelphys results from the absence of fusion of the bilateral mullerian ducts. It is a rare pathology. This malformation concerns 5% of uterine malformations from mullerian ducts and affects one woman in 1,000-30,000. Obstetrical complications
Andrianampanalinarivo, Hery R., Fleurian, Sidy, IA, Housni, Rakotomboahangy, Todisoa M., Randriamahavonjy, Romuald, Ratsiatosika, Tanjona A., Solange, Rasoanandrianina B.   +6 more
core   +2 more sources