Anterior urethral hamartoma in a female infant with anorectal malformation: A rare case report and literature review.

Introduction And Importance: Urethral hamartoma is highly unusual, as documented in the literature with only one case that ever reported. Here, we report a case of female infant with urethral hamartoma and anorectal malformation.

Case Presentation: An 8 months old female infant was previously diagnosed with anorectal malformation (ARM) with rectovestibular fistula that had underwent colostomy.