نتایج جستجو برای: esophageal atresia
تعداد نتایج: 56110 فیلتر نتایج به سال:
Congenital esophageal atresia needs to be surgically corrected as soon as possible. Some will present with post surgical stricture that needs to be dilated by a balloon dilator. This procedure is difficult in premature born due to infant esophageal size and availability of equipments. We herby report the first case in a premature infant with post surgical esophageal stricture of esophageal atre...
conclusions elective gastric pull up can be performed for children who are not above 10 kg. in such settings, the risk of respiratory infections and other complications would be significantly reduced because of shorter duration of intubation. results the mean age was 5 ± 2 years in patients who were above 10 kg and 3 ± 1 years in those less than 10 kg. patients who were less than 10 kg had shor...
How to cite: Gharpure V. Esophageal atresia with/without tracheoesophageal fistula. QUESTIONS 1. What clinical and sonographic features should make one suspect esophageal atresia in a pregnancy? 2. What is the quickest method of diagnosing esophageal atresia, with or without tracheo-esophageal fistula (TEF)? 3. What management principles should be followed in a newborn with esophageal atresia ±...
Background & Aim: Esophageal replacement is done for patients with long gap esophageal atresia, severe stenosis of esophagus due to gastroesophageal reflux, and burns due to chemical agents. A suitable replacement for esophagus must have the following qualities: appropriate function, no tendency to malignancy, straight direction, no gastroesophageal reflux, and fewer complications. Today ga...
Esophageal replacement in children: presentation of 18 cases and results of their surgical procedure
Abstract Background: Esophageal replacement is indicated in certain circumstances including long gap esophageal atresia, severe strictures due to gastro-esophageal reflux (GER) and caustic burns. We analyzed our results of 18 patients who underwent esophageal replacement in our university hospital. Methods: We reviewed esophageal replacements carried out in our department between June 1996 and...
congenital esophageal atresia needs to be surgically corrected as soon as possible. some will present with post surgical stricture that needs to be dilated by a balloon dilator. this procedure is difficult in premature born due to infant esophageal size and availability of equipments. we herby report the first case in a premature infant with post surgical esophageal stricture of esophageal atre...
Introduction: Esophageal atresia is one of the most significant congenital diseases in pediatric surgery. Postoperative complications have become an important issue. Additionally, the little data are about life quality of baby's that had been surgery. The aim of our study was to analyze and evaluating the long- term life quality of subjects. Methods: We performed an observational study of the...
esophageal replacement in children: presentation of 18 cases and results of their surgical procedure
abstract background: esophageal replacement is indicated in certain circumstances including long gap esophageal atresia, severe strictures due to gastro-esophageal reflux (ger) and caustic burns. we analyzed our results of 18 patients who underwent esophageal replacement in our university hospital. methods: we reviewed esophageal replacements carried out in our department between june 1996 and ...
Diverse therapies for the management of anastomotic leakage after esophageal atresia repair have been reported with various outcomes. The surgical management of anastomotic leakage after esophageal atresia repair can be challenging. We present a child with long-gap esophageal atresia and anastomotic leakage repair with pericardium. This article aimed to illustrate that pericardium may be a subs...
Combination of congenital esophageal atresia and subsequent hypertrophic pyloric stenosis is a rare condition which occurs in early infancy. The underlying etiology and pathophysiology of this association still remains unclear. In this paper we report a unique case of hypertrophic pyloric stenosis, for the first time, which occurred in an infant who underwent surgery for type I esophag...
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