{"title":"孤立性先天性尿道皮肤瘘：两份病例报告","authors":"U. Munmun, A. Z. Hossain","doi":"10.3329/jpsb.v10i1.72650","DOIUrl":null,"url":null,"abstract":"A common complication after hypospadias surgery is a urethrocuteneous fistula. But when it is congenital and present in isolated form, it becomes extremely uncommon and usually present in the paediatric age group and associated with hypospadias, chordee, or anorectal malformation. In this report, we are presenting 2 cases of uncircumcised boys with this rare entity of Isolated congenital anterior uretrocuteneous fistula, highlighting etiology, embryology, and surgical reconstructions for management.\nJournal of Paediatric Surgeons of Bangladesh (2019) Vol. 10 (1 & 2): 62-65","PeriodicalId":137868,"journal":{"name":"Journal of Paediatric Surgeons of Bangladesh","volume":"7 8","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolated congenital urethrocutaneous fistula: Two case reports\",\"authors\":\"U. Munmun, A. Z. Hossain\",\"doi\":\"10.3329/jpsb.v10i1.72650\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A common complication after hypospadias surgery is a urethrocuteneous fistula. But when it is congenital and present in isolated form, it becomes extremely uncommon and usually present in the paediatric age group and associated with hypospadias, chordee, or anorectal malformation. In this report, we are presenting 2 cases of uncircumcised boys with this rare entity of Isolated congenital anterior uretrocuteneous fistula, highlighting etiology, embryology, and surgical reconstructions for management.\\nJournal of Paediatric Surgeons of Bangladesh (2019) Vol. 10 (1 & 2): 62-65\",\"PeriodicalId\":137868,\"journal\":{\"name\":\"Journal of Paediatric Surgeons of Bangladesh\",\"volume\":\"7 8\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Paediatric Surgeons of Bangladesh\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/jpsb.v10i1.72650\",\"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 Paediatric Surgeons of Bangladesh","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/jpsb.v10i1.72650","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Isolated congenital urethrocutaneous fistula: Two case reports
A common complication after hypospadias surgery is a urethrocuteneous fistula. But when it is congenital and present in isolated form, it becomes extremely uncommon and usually present in the paediatric age group and associated with hypospadias, chordee, or anorectal malformation. In this report, we are presenting 2 cases of uncircumcised boys with this rare entity of Isolated congenital anterior uretrocuteneous fistula, highlighting etiology, embryology, and surgical reconstructions for management.
Journal of Paediatric Surgeons of Bangladesh (2019) Vol. 10 (1 & 2): 62-65
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