Currarino Triad

  • Choi, Kwang-Hae (Department of Pediatrics, Seoul National University, College of Medicine) ;
  • Chung, Ju-Young (Department of Pediatrics, Seoul National University, College of Medicine) ;
  • Bae, Sun-Hwan (Department of Pediatrics, Seoul National University, College of Medicine) ;
  • Ko, Jae-Sung (Department of Pediatrics, Seoul National University, College of Medicine) ;
  • Kim, Woo-Sun (Department of Radiology, Seoul National University, College of Medicine) ;
  • Kim, In-One (Department of Radiology, Seoul National University, College of Medicine) ;
  • Seo, Jeong-Kee (Department of Pediatrics, Seoul National University, College of Medicine)
  • 최광해 (서울대학교 의과대학 소아과학교실) ;
  • 정주영 (서울대학교 의과대학 소아과학교실) ;
  • 배선환 (서울대학교 의과대학 소아과학교실) ;
  • 고재성 (서울대학교 의과대학 소아과학교실) ;
  • 김우선 (서울대학교 의과대학 진단방사선과학교실) ;
  • 김인원 (서울대학교 의과대학 진단방사선과학교실) ;
  • 서정기 (서울대학교 의과대학 소아과학교실)
  • Received : 1998.08.11
  • Accepted : 1998.09.08
  • Published : 1999.03.30

Abstract

Currarino triad is a hereditary condition diagnosed when three abnormalities are noted: (1) an anorectal malformation; (2) an anterior sacral defect and (3) a presacral mass. We experienced 3 cases of Currarino triad with severe constipation. All cases had presacral mass and sacral bony defect. One case had rectovaginal fistula, other one case had holoprosencephaly. Presacral masses were lipomeningomyelocele and epidermoid or dermoid cyst. We report three cases of Currarino triad with brief review of the related literature.

Keywords