Congenital pouch colon (CPC) is a rare form of anorectal malformation, in which the entire colon is replaced by an enormously dilated pouch that communicates with a fistula to the genitourinary tract. CPC is a condition which comprises of a high form of anorectal malformation which is associated with large variations in the size of the dilatations of the affected colonic segment. Surgical management depends on the type of CPC, and outcomes are variable depending on the length of colon affected and the anorectal muscle complex.
CITATION STYLE
Saxena, A. K., & Mathur, P. (2020). Congenital Pouch Colon. In Pediatric Surgery: General Principles and Newborn Surgery: Volume 1 (Vol. 1, pp. 1087–1098). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-662-43588-5_77
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