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Type-A long-gap esophageal atresia treated by thoracoscopic elongation and subsequent radical surgery : a case report Kenichiro KONISHI 1 , Tetsuya ISHIMARU 1 , Hiroshi KAWASHIMA 1 , Masahiko SUGIYAMA 1 , Hiroaki KOMURO 1 , Tadashi IWANAKA 1 1Department of Pediatric Surgery, The University of Tokyo Hospital Keyword: A型long gap食道閉鎖・胸腔鏡・食道延長術 pp.241-246
Published Date 2015/5/15
DOI https://doi.org/10.11477/mf.4426200129
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 A girl was born at 36 weeks of gestation weighing 1,835 g. She was diagnosed with Type-A esophageal atresia by chest and abdominal x-ray. When she underwent a gastrostomy on day one after birth, she was diagnosed as having a gap length of 3 vertebrae. Thoracoscopic elongation surgery(modified Foker technique) was performed at 9 days old, and her weight was then 1,669 g. The gaps were shortened by 1.5 vertebrae in one week. Radical thoracoscopic repair for esophageal atresia was performed at the age of 22 days when her weight was 1,952 g. For postoperative anastomotic stenosis, balloon dilation was performed, and then, she started taking milk orally. Type-A long-gap esophageal atresia commonly requires elongation surgery followed by radical surgery or esophageal replacement after weight growth. Elongation surgery(Foker technique) required two open procedures previously, but we performed both elongation surgery and subsequent radical surgery thoracoscopically. Therefore, we kept musculoskeletal problems to a minimum, and her parents are also satisfied with the cosmetic appearance of the three small wounds.


Copyright © 2015, JAPAN SOCIETY FOR ENDOSCOPIC SURGERY All rights reserved.

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電子版ISSN 2186-6643 印刷版ISSN 1344-6703 日本内視鏡外科学会

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