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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 HeePark, Sung BinLee, Yu JinLee, Kyung SangLee, 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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