2004
DOI: 10.1007/s00383-004-1162-2
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Congenital pouch colon associated with anorectal agenesis

Abstract: This article presents a review of the history and development of the various types of congenital pouch colon. Also described are the criteria for diagnosis, the treatment modalities and the results of follow-up studies to emphasize the post-operative problems. The problem of pre-operative and post-operative fecal incontinence is dealt with in more detail.

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Cited by 29 publications
(74 citation statements)
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References 23 publications
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“…Continence has been assessed in our patients using the Kelly's score and 80% show a good result, 7.5% a fair result and 12.5% a poor result. These figures are actually better than the continence scores of a corresponding set of patients with supralevator anorectal malformation and contrast with the experience of other authors [8,14]. In the absence of colonic dilatation, there is no enterocolitis.…”
Section: Discussioncontrasting
confidence: 44%
See 1 more Smart Citation
“…Continence has been assessed in our patients using the Kelly's score and 80% show a good result, 7.5% a fair result and 12.5% a poor result. These figures are actually better than the continence scores of a corresponding set of patients with supralevator anorectal malformation and contrast with the experience of other authors [8,14]. In the absence of colonic dilatation, there is no enterocolitis.…”
Section: Discussioncontrasting
confidence: 44%
“…Window colostomy is associated with a 25% incidence of problems like prolapse, stenosis and pouch eversion with intra-colostomy hernia in our hands, but these have been manageable and have not adversely affected the final outcome. Once window colostomy has been performed, the colo-urinary fistula narrows down to a very small lumen (though the external size of the connection is 1-5 to 2-cm-wide) and we have not seen urinary reflux into the pouch in our patients as reported by other authors [7,8]. In fact when the fistula is divided at surgery it is quite difficult to find the opening in the bladder due to its small size.…”
Section: Discussionsupporting
confidence: 43%
“…The two terms most commonly used to describe this anomaly are congenital short colon and congenital pouch colon. [16][17][18][19][20][21][22][23][24] The anatomy of this malformation was first described in 1977 by Singh et al and subsequently in detail by Wakhlu et al and Chadha et al [25][26][27] An important advancement in the management of this condition was the technique of coloplasty in 1976 by Chiba et al…”
mentioning
confidence: 99%
“…The cases of pouch colon are mostly found in Asian countries especially in India with maximum number of cases reported from Northern India. [4] However, the outcome of the surgery of these conditions often remains unsatisfactory. [5,6] This may partly be due to nonavailability of functional studies in terms of contractility of intestinal smooth muscles because most of the studies so far conducted on these disorders were focused on histology and immunohistochemistry.…”
Section: Introductionmentioning
confidence: 99%