Menouria due to congenital vesicovaginal fistula associated with complex genitourinary malformation
Autor: | N Rajamaheshwari, K Seethalakshmi, Lilly Varghese |
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Jazyk: | angličtina |
Rok vydání: | 2009 |
Předmět: | |
Zdroj: | Indian Journal of Urology, Vol 25, Iss 4, Pp 534-536 (2009) |
Druh dokumentu: | article |
ISSN: | 0970-1591 1998-3824 |
DOI: | 10.4103/0970-1591.57924 |
Popis: | Background: Congenital vesicovaginal fistula (VVF) is a very uncommon condition rarely suspected at initial presentation. It is usually seen in association with complex malformations of the genitourinary tract. Case: A bifid insertion of the solitary ureter causing an uretero-VVF was associated with an obstructing transverse vaginal septum manifesting as menouria. Also seen were solitary crossed renal ectopia, bicornuate uterus and skeletal anomalies. Conclusion: In women with menouria without vaginal menstruation, pre-operative evaluation to detect an obstructive vaginal anomaly and unusual uretero-vesicovaginal fistulous communications is necessary before surgical intervention. |
Databáze: | Directory of Open Access Journals |
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