Herlyn-Werner-Wunderlich syndrome: uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Sonographic and MR findings in 11 cases
- 15 May 2007
- journal article
- Published by Springer Science and Business Media LLC in Pediatric Radiology
- Vol. 37 (7), 657-665
- https://doi.org/10.1007/s00247-007-0497-y
Abstract
Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis is a rare entity, sometimes referred to as Herlyn-Werner-Wunderlich syndrome (HWW). It usually presents after menarche with progressive pelvic pain, sometimes with regular menses, and a palpable mass due to hemihaematocolpos. The diagnosis is generally made only if the suspicion of this genitourinary syndrome is raised.Keywords
This publication has 36 references indexed in Scilit:
- Multicystic dysplastic kidney with ipsilateral abnormalities of genitourinary tract: Experience in childrenUrology, 2006
- Uterus Didelphys with Obstructed Hemivagina and Multicystic Dysplastic KidneyEuropean Journal of Pediatric Surgery, 2005
- Didelphic uterus and obstructed hemivagina with renal agenesis: case report and review of the literatureJournal of Pediatric and Adolescent Gynecology, 2004
- Ultrasound of female genital anomaliesEuropean Radiology Supplements, 2004
- MRI in the evaluation of müllerian duct anomaliesClinical Imaging, 2003
- MRI Appearances of Müllerian Duct AbnormalitiesClinical Radiology, 2003
- Diagnosing Neonatal Female Genital Anomalies Using Saline-Enhanced SonographyAmerican Journal of Roentgenology, 2001
- Double uterus, blind hemivagina, and ipsilateral renal agenesis: 36 cases and long-term follow-upObstetrics & Gynecology, 1997
- MR imaging of Müllerian anomalies: impact on therapy.American Journal of Roentgenology, 1996
- A Case of Unilateral Hæmatokolpos, Hæmatometra and Hæmatosalpinx.BJOG: An International Journal of Obstetrics and Gynaecology, 1922