Autor: |
Singh, Aditya Pratap, Barolia, Dinesh Kumar, Bathia, Harsha Vinod, Parmar, Vipal H., Mehta, Bhavana Asit, Mehta, Shraddha |
Předmět: |
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Zdroj: |
Journal of Pediatric & Adolescent Surgery; 2021, Vol. 2 Issue 1, p1-3, 3p |
Abstrakt: |
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. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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