Article citationsMore>>
Hutson, J., Peña, A., Beket, E., Chatterjee, S., Coran, A., Davies, M., Georgeson, K., Grosfeld, J., Gupta, D., Iwai, N., Kluth, D., Martucciello, G., Moore, S., Rintala, R., Durham Smith, E., Sripathi, D.V., Stephens D. and Kunst, M. (2005) Preliminary Report on the International Conference for the Development of Standards for the Treatment of Anorectal Malformations. Journal of Pediatric Surgery, 40, 1521-1526.
https://doi.org/10.1016/j.jpedsurg.2005.08.002
has been cited by the following article:
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TITLE:
Isolated Caeco-Vesical Fistula: A Case Report
AUTHORS:
Lucienne Irène Patricia Ondima, Melvin Ondongo Atipo, Steve Aristide Ondziel Opara, Didace Massamba-Miabaou, Régis Moyikoua, Peggy Dalhia Galou Mawandza, Moïse Yanguedet Service, Caryne Mboutol-Mandavo, Pierre Aymar Oko, Jean-Claude Mieret, Cardinale Princilia Okiemy Niendet, Gracia Christelle Ossete, Erica Nuptia Akobande, Anani Wenceslas Séverin Odzébé, Prosper Bouya
KEYWORDS:
Fistula, Congenital, Isolated, Caecum, Bladder, Child, Surgery
JOURNAL NAME:
Open Journal of Urology,
Vol.10 No.12,
December
31,
2020
ABSTRACT: Congenital uro or genito-digestive fistulas are frequently found in the context of caudal pole malformations. Isolated congenital forms without associated anorectal malformation have not been reported until now. We report the first case we know a 9 year old female child received in a pediatric surgery consultation for fecaluria evolving since birth with a permeable anus. She presented a good general condition, a good staturo-ponderal and psychomotor development, a vulva soiled by stool and a permeable anus with a tonic sphincter. A retrograde urethrocystography revealed a caeco-vesical fistula. Surgery consisted of ligation-section of the caeco-vesical septum. A follow-up urethrocystography at three months post-surgery no longer visualized the fistula. Our post-operative follow-up is 4 years. Isolated congenital caeco-vesical fistula is an unknown pathology whose late diagnosis can have serious repercussions.