Uterus didelphys with blind hemivagina and ipsilateral renal agenesis (Herlyn-Werner-Wunderlich syndrome) suspected on the presence of hydrocolpos on prenatal sonography
- Authors
- Han, Byoung Hee; Park, Sung Bin; Lee, Yu Jin; Lee, Kyung Sang; Lee, Yeon Kyung
- Issue Date
- Jul-2013
- Publisher
- WILEY-BLACKWELL
- Keywords
- Herlyn-Werner-Wunderlich syndrome; obstetrics; uterus; Mullerian duct anomaly; hydrometrocolpos; ultrasound; gynecology
- Citation
- JOURNAL OF CLINICAL ULTRASOUND, v.41, no.6, pp 380 - 382
- Pages
- 3
- Journal Title
- JOURNAL OF CLINICAL ULTRASOUND
- Volume
- 41
- Number
- 6
- Start Page
- 380
- End Page
- 382
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/71300
- DOI
- 10.1002/jcu.21950
- ISSN
- 0091-2751
1097-0096
- Abstract
- We report the case of a female neonate with ipsilateral renal agenesis and uterus didelphys with blind hemivagina, also known as Herlyn-Werner-Wunderlich (HWW) syndrome. Prenatal sonography revealed the absence of the left kidney and a retrovesical cystic lesion suspected as hydrometrocolpos. Postnatal evaluation confirmed that the cystic lesion was a hydrocolpos associated with double uterus and blind hemivagina (HWW syndrome). HWW syndrome can be suspected prenatally if a retrovesical cystic lesion is detected in a female fetus with unilateral absence of kidney. (c) 2012 Wiley Periodicals, Inc. J Clin Ultrasound 41:380-382, 2013
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