D. Barolia, A. Singh, H. Bathia, Vipal H Parmar, B. Mehta, S. Mehta
{"title":"女性新生儿直肠闭锁伴袋结肠无瘘-罕见的关联:1例报告","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":"{\"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}","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}
Rectal atresia with pouch colon without fistula in a female newborn– a rare association: A case report
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.