D. Barolia, A. Singh, H. Bathia, Vipal H Parmar, B. Mehta, S. Mehta
{"title":"Rectal atresia with pouch colon without fistula in a female newborn– a rare association: A case report","authors":"D. Barolia, A. Singh, H. Bathia, Vipal H Parmar, B. Mehta, S. Mehta","doi":"10.46831/jpas.v2i1.102","DOIUrl":null,"url":null,"abstract":"Background: Rectal atresia is a rare variant of anorectal malformation (ARM). Pouch colon is an abnormal dilation of the colon distally connected by the fistula. Pouch colon without fistula is extremely rare.\nCase Presentation: We report a case of unusual association of rectal atresia with pouch colon without fistula in a female newborn. At surgery, a type IV pouch colon was found which was resected and colostomy was done as the initial procedure.\nConclusion: Rectal atresia with congenital pouch colon without genitourinary fistula in a female child is an extremely rare association.","PeriodicalId":335209,"journal":{"name":"Journal of Pediatric and Adolescent Surgery","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric and Adolescent Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46831/jpas.v2i1.102","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Rectal atresia is a rare variant of anorectal malformation (ARM). Pouch colon is an abnormal dilation of the colon distally connected by the fistula. Pouch colon without fistula is extremely rare.
Case Presentation: We report a case of unusual association of rectal atresia with pouch colon without fistula in a female newborn. At surgery, a type IV pouch colon was found which was resected and colostomy was done as the initial procedure.
Conclusion: Rectal atresia with congenital pouch colon without genitourinary fistula in a female child is an extremely rare association.
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