선천성 식도 폐쇄증에 대한 임상적 고찰

A Clinical Review of Esophageal Atresia : One Surgeon's Experience

  • 김성식 (한양대학교 의과대학 소아외과) ;
  • 임시연 (한양대학교 의과대학 소아외과) ;
  • 정풍만 (한양대학교 의과대학 소아외과)
  • Kim, Sung-Sik (Department of Surgery, College of Medicine, Hanyang University) ;
  • Rhim, Si-Youn (Department of Surgery, College of Medicine, Hanyang University) ;
  • Jung, Poong-Man (Department of Surgery, College of Medicine, Hanyang University)
  • 투고 : 2007.07.03
  • 심사 : 2008.06.23
  • 발행 : 2008.06.30

초록

From 1979 to 2006, fifty eight patients with esophageal atresia were treated by one pediatric surgeon at Hanyang University Hospital. We analyzed the clinical findings and outcome of these 58 patients. There were 30 males and 28 females. Their mean birth weight was $2,960{\pm}400g$ (1,170~4,020 g). The most common type of anomaly was Gross type C (49 patients; 84.5 %). There was no type B. Fifty-two patients underwent definitive surgery. Postoperative complications were as follows: anastomotic leakage in 17 patients (32.7 %), anastomotic site stricture in 15 (28.8 %), gastroesophageal reflux in 10 (19.2 %) and recurrent TEF in 1 (1.9 %). A total of 152 associated anomalies were detected from 48 patients (82.2 %). The cardiovascular system was the most commonly affected (30 patients with 46 anomalies). The VACTERL association was present in 14 patients (24.1 %). Operative mortality was 17.3 % including self-discharge patients after operation.

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