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经胸、胸膜外Ⅰ期手术治疗食管闭锁

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摘要 食管闭锁(esophageal atresia,ET)是以食管连续性中断为特征的先天性发育畸形,可伴有或不伴有气管食管瘘,ET最常见的类型是近段食管闭锁并远段气管食管瘘,占总数的86%。食管闭锁的发生率为2500—4500个活产儿中1个。其严重危及患儿生命,需要急诊手术矫治。自1943年Haight和Towsley报告了第1例Ⅰ期食管吻合成功的病例至今已有近70年。早期的手术死亡率高达30%~50%。
作者 陈永卫
出处 《临床外科杂志》 2010年第8期508-509,共2页 Journal of Clinical Surgery
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参考文献10

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二级参考文献5

  • 1[1]Spitz L,Kiely EM,Morecroft JA,Drake DP.Oesophageal atresia:at risk groups for the 1990's.J Pediatr Surg 1994;29:723-725. 被引量:1
  • 2叶蓁蓁.对提高食管闭锁存活的几点意见[J].中华小儿外科杂志,1993,(14):371. 被引量:2
  • 3[4]Nambirajan L,Rintala RJ,Losty PD et al.The value of early postoperative oesophagography following repair of oesophageal atresia.Pediatr Surg Int 1998; 13:1881-1883. 被引量:1
  • 4[5]Chittmittrapap S,Spitz L,Kiely EM et al.Anastomotic stricture following repair of esophageal atrisial J Pediatr Surg 1990;25:508-511. 被引量:1
  • 5[6]Koivusalo A,Turunen P,Rintala RJ et al.Is routine dilatation after repair of esophageal atresia with distal fistula better than dilatation when symptoms arise? Comparison of results of two European pediatric surgical centers.J Pediatr Surg.2004 Nov;39(11):1643-7. 被引量:1

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