선천성 식도폐쇄에서 발생한 선천성 기관연화

Congenital Tracheomalacia Associated with Esophageal Atresia

  • 한석주 (연세대학교 외과학교실) ;
  • 정은주 (연세대학교 외과학교실) ;
  • 김세헌 (연세대학교 이비인후과교실) ;
  • 윤춘식 (연세대학교 진단방사선과학교실) ;
  • 심규대 (연세대학교 마취과학교실) ;
  • 남용택 (연세대학교 마취과학교실) ;
  • 김재억 (연세대학교 소화아동병원 소아외과) ;
  • 황의호 (연세대학교 외과학교실)
  • Han, Seok-Joo (Department of Surgery, Yonsei University College of Medicine) ;
  • Jung, Eun-Joo (Department of Surgery, Yonsei University College of Medicine) ;
  • Kim, Se-Heon (Department of Otolaryngology, Yonsei University College of Medicine) ;
  • Yoon, Choon-Sik (Department of Radiology, Yonsei University College of Medicine) ;
  • Shim, Kyu-Dae (Department of Anesthesiology, Yonsei University College of Medicine) ;
  • Nam, Yong-Taek (Department of Anesthesiology, Yonsei University College of Medicine) ;
  • Kim, Jai-Eok (Department of Pediatric Surgery, Sowha Children's Hospital Yonsei University College of Medicine) ;
  • Hwang, Eui-Ho (Department of Surgery, Yonsei University College of Medicine)
  • 발행 : 2002.12.30

초록

This is a case of tracheomalacia associated with esophageal atresia. An 11-month-old- male boy presented with a life-threatening apneic spell after correction of esophageal atresia (Gross type C). After complete exclusion of the other possible causes of the apneic spell, the presumptive diagnosis of tracheomalacia was made with fluoroscopy and 3-dimensional chest CT. The final diagnosis was made with rigid bronchoscopy under spontaneous respiration. The aortopexy was performed with intraoperative bronchoscopic examination. The postoperative period was unremarkably uneventful. The patient was discharged 9 days after the aortopexy and has remained well to date (5 months after the aortopexy).

키워드