Pure esophageal atresia. 2 case

  • Jeong, Sang-Seok (Department of Thoracic and Cardiovascular Surgery, College of Medicine, Dong-A University) ;
  • Choi, Phil-Jo (Department of Thoracic and Cardiovascular Surgery, College of Medicine, Dong-A University) ;
  • Park, Kwon-Jae (Department of Thoracic and Cardiovascular Surgery, College of Medicine, Dong-A University) ;
  • Bang, Jung-Hee (Department of Thoracic and Cardiovascular Surgery, College of Medicine, Dong-A University) ;
  • Cho, Gwang-Jo (Department of Thoracic and Cardiovascular Surgery, College of Medicine, Dong-A University) ;
  • Woo, Jong-Soo (Department of Thoracic and Cardiovascular Surgery, College of Medicine, Dong-A University) ;
  • Jung, Jin-A (Department of Pediatrics, College of Medicine, Dong-A University)
  • 정상석 (동아대학교병원 흉부외과학교실) ;
  • 최필조 (동아대학교병원 흉부외과학교실) ;
  • 박권재 (동아대학교병원 흉부외과학교실) ;
  • 방정희 (동아대학교병원 흉부외과학교실) ;
  • 조광조 (동아대학교병원 흉부외과학교실) ;
  • 우종수 (동아대학교병원 흉부외과학교실) ;
  • 정진아 (동아대학교병원 소아과학교실)
  • Published : 2008.06.30

Abstract

Pure esophageal atresia without tracheoesophageal fistula is a uncommon form of congenital malformation of the esophagus, which is able to be suspected by fetal ultrasonograpy before delivery and diagnosed definitely by simple chest X-ray and esophagogram immidiately after delivery. We performed delayed primary repair in 2 cases of pure esophageal atresia by using stomach for conduit in one case and colon in the other case. But there were graft failure in the latter case, so reoperation was performed by using stomach. Postoperatively, two patients showed no stenosis and leakage in anastomotic site and were discharged in good oral intake without dysphagia.

Keywords