Acta Pediátrica de México (Jul 2014)

Colon pouch syndrome. In the spectrum of the anorectal malformaciotions

  • Santos Jasso Karla Alejandra,
  • Palestina Carro Oscar

DOI
https://doi.org/10.18233/APM34No3pp132-140
Journal volume & issue
Vol. 34, no. 3
pp. 132 – 140

Abstract

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Congenital colon pouch syndrome, is an infrequent clinical condition in which the colon is totally o partially replaced by a cystic dilatation, and is associated with an anorectal malformation; which may be a urinary tract fistula, a vaginal or vestibule fistula, or a cul-de-sac. We present a rare variant of the anorrectal malformation, with two cases of colon pouch types II and III respectively. The diagnosis was suspected in a plain X-ray and on a distal colostogram. It was confirmed during surgery. The controversial aspects of surgical options are discussed, and emphasis is made on the importance of the follow-up of patients with anorectal malformations, including the need for bowel rehabilitation.

Keywords