Hématocolpos par hémivagin borgne. À propos de trois cas

Ceccaldi, Pierre-François; Ducarme, Guillaume; Dedecker, F; Harika, G; Gabriel, Rosalina; Quereux, C.; Graesslin, Olivier

doi:10.1016/j.gyobfe.2006.02.019

Cited by 3 publications

(2 citation statements)

References 12 publications

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“…Different devices have been put in place to overcome this problem, in particular with the introduction of a specific intravaginal mold 3 nights a week for 4 to 6 months. The application of hyaluronic acid has shown its success in preventing recurrent stenosis [ 10 ].…”

Section: Discussionmentioning

confidence: 99%

Surgical management of a transverse vaginal septum: About a rare case

El Abbassi,

Bensouda,

Jalal

et al. 2023

International Journal of Surgery Case Reports

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Section: Discussionmentioning

confidence: 99%

Surgical management of a transverse vaginal septum: About a rare case

El Abbassi,

Bensouda,

Jalal

et al. 2023

International Journal of Surgery Case Reports

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“…The malformations of the urinary tract appear at the same time when Wolf's (mesonephric) and Müller's (paramesonephric) ducts are topographically close; renal agenesis, reported in several series is almost constant. 9 The exact etiology of this malformation is unknown, however, genetic, environmental and endocrine factors may be incriminated. 8 According to the different classifications, this anomaly is classified as type III according to the American Fertility Society and U3bC2V2 according to the new ESHRE classification, there are other variants of this pathology: the blind hemivagina with renal agenesis can be associated with a septate or total bicornuate uterus instead of a didelphic uterus (U2b according to ESHRE and Iva or Va according to AFSM).…”

Section: Introductionmentioning

confidence: 99%

A rare urogenital malformation “Herlyn-Werner-Wunderlich syndrome” (Ohvira syndrome) discovered during an acute pelvic pain

Kamal

Ayoub

Ibtissam

et al. 2023

Int J Reprod Contracept Obstet Gynecol

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The Herlyn-Werner-Wunderlich syndrome (OHVIRA syndrome) is a rare urogenital malformation, characterized by a blind hemivagina, a didelphic uterus, and homolateral renal agenesis, it results from a defect in the development of the muller and Wolf ducts during the embryonic period, of unknown origin, the diagnosis is most often made at puberty during the first menstruation, sometimes late, particularly for non-obstructive forms: infertility or obstetrical complications, the diagnosis is based on pelvic ultrasound especially with 3D reconstructions and pelvic magnetic resonance imaging (MRI) which remains the standard gold for the detection of mullerian anomalies, laparoscopy can also play a double diagnostic and prognostic role in order to study the consequences of the blood reflection (hematosalpinx, inflammatory pelvis, endometriosis. In this work we report the case of an OHVIRA syndrome diagnosed late at the age of 36 years in a multiparous woman with acute pelvic pain simulating the picture of a torsion of the adnexa, we will discuss through this case the clinical, diagnostic and therapeutic aspects of this uterine malformation.

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