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Int J Surg Case Rep · Jan 2013
Delayed primary reconstruction of esophageal atresia and distal tracheoesophageal fistula in a 471-g infant.
- Keiichi Ito, Shuichi Ashizuka, Masashi Kurobe, Shinsuke Ohashi, Naruo Kuwashima, Joji Yoshizawa, and Takao Ohki.
- Division of Pediatric Surgery, Department of Surgery, The Jikei University School of Medicine, Tokyo, Japan. Electronic address: keke-ito@jikei.ac.jp.
- Int J Surg Case Rep. 2013 Jan 1;4(2):167-9.
IntroductionWaterston et al. have classified the risk of morbidity in infants with esophageal atresia and tracheoesophageal fistula. However, few cases of esophageal atresia with distal tracheoesophageal fistula in extremely low birth weights infants have been reported. In such infants, the selection of primary reconstruction or staged repair remains controversial. In the present report, we describe the difficulties of perioperative management of such small infants and discuss how to rescue them.Presentation Of CaseA 471-g female infant was delivered at 28 weeks' gestation via cesarean section. Esophageal atresia with distal tracheoesophageal fistula was diagnosed. Esophageal banding and gastrostomy were performed via laparotomy on day 1. On day 74, when the infant weighed almost 1000g, airway management was discontinued. On day 136, endotracheal intubation again became necessary because of respiratory problems, and the esophagus was reconstructed on day 141. Despite this operation, the patient died on day 276 because of continuing respiratory problems.DiscussionEsophageal banding is considered an appropriate treatment for respiratory problems in such extremely low weight infants. However, the timing of dissection of the tracheoesophageal fistula after esophageal banding is extremely important.ConclusionIn the present case, ligation of the tracheoesophageal fistula and esophageal reconstruction should have been performed as soon as possible.Copyright © 2012 Surgical Associates Ltd. Published by Elsevier Ltd. All rights reserved.
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