Herlyn-Werner-Wunderlich syndrome (uterus didelphys, blind hemivagina and ipsilateral renal agenesis) – a case report
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Case Report
VOLUME: 11 ISSUE: 2
P: 107 - 109
June 2010

Herlyn-Werner-Wunderlich syndrome (uterus didelphys, blind hemivagina and ipsilateral renal agenesis) – a case report

J Turk Ger Gynecol Assoc 2010;11(2):107-109
1. Department Of Obstetrics And Gynecology, Faculty Of Medicine, Zonguldak Karaelmas University, Zonguldak, Turkey
2. Department Of Obstetrics And Gynecology, Harran University Faculty Of Medicine, Sanliurfa, Turkey
3. Karaelmas University, School Of Medicine, Department Of Obstetrics And Gynecology, Zonguldak, Turkey
No information available.
No information available
Received Date: 13.11.2009
Accepted Date: 16.12.2009
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ABSTRACT

Uterovaginal duplication with obstructed hemivagina and ipsilateral renal agenesis is referred to as the Herlyn-Werner-Wunderlich (HWW) syndrome. A 17 year old woman presented with right pelvic pain and dysmenorrhea, present since menarche at 13 and worsening over the past year. Ultrasound examination revealed a right pelvic mass (5x5 cm), double endometrial echoes, and hematocolpos. A right pelvic mass, agenesis of the right kidney, double uterus, and blind hemivagina with hematocolpos were detected by magnetic resonance imaging and intravenous pyelography. A right tubo-ovarian abscess with dense adhesions and a double uterus were observed on diagnostic laparoscopy. Adhesiolysis was carried out and purulent material irrigated. After a course of antibiotics, a vaginal septum resection was performed and the pyocolpos drained. She remained symptom free after four months of follow-up. Prompt and accurate diagnosis and treatment of this syndrome can significantly improve the lives of sufferers and prevent future complications.

Keywords:
Blind hemivagina, Herlyn-Werner-Wunderlich syndrome, Müllerian duct anomaly, Pyocolpos, Uterus didelphys