WITHDRAWN: Thoracic H-type Tracheoesophageal fistula after repair of anorectal malformation in neonate

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منابع مشابه

Congenital H-type tracheoesophageal fistula.

A 12-year-old girl with H-type tracheoesophageal fistula is presented. The fistula was proven by bronchoscopic, oesophageoscopic and radiographic (with contrast medium) studies. As a sucking child the girl was operated, but there is no medical documentation (the girl is a displaced person). The question remains whether it is a primary or recurrent fistula.

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Early Recognition of H-Type Tracheoesophageal Fistula

Tracheoesophageal fistula (TEF) without associated esophageal atresia (EA) is a rare congenital anomaly. Diagnosis in neonatal period is usually not made and most of the patients are treated as cases of pneumonia. A case of H-type of tracheoesophageal fistula, diagnosed within 24 hours of delivery based upon choking and cyanosis on first trial of feed, is being reported. Diagnosis was confirmed...

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Isolated Tracheoesophageal Fistula – a Rare Congenital Malformation

Introduction: Isolated congenital tracheoesophageal fistula is a very rare malformation with an incidence of 1 in 50.000-80.000 births. In most of the cases this anomaly is detected in the first year of life because of the suggestive symptoms, but sometimes the diagnosis is delayed even until adulthood. Aim: The purpose of this paper is to analyse clinical, imagistic and therapeutic sights of t...

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Simplified access for division of the low cervical/high thoracic H-type tracheoesophageal fistula.

H-type tracheoesophageal fistulas (H-TEF) often are located in the low cervical/high thoracic region where determination of the most appropriate surgical approach is difficult. When it can provide adequate exposure, a cervical incision is preferred because of the likelihood of decreased morbidity. A child with VACTERL association presented with recurrent respiratory problems. Esophagogram showe...

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Lung torsion after tracheoesophageal fistula repair in an infant

Lung torsion is a very rare event that has been reported in only 9 cases in the pediatric literature but has not yet been reported in Korean infants. We present a case of lung torsion after tracheoesophageal fistula repair in an infant. Bloody secretion from the endotracheal tube and chest radiographs and computed tomographic scan results indicated lung torsion. Emergency exploration indicated ...

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ژورنال

عنوان ژورنال: Journal of Pediatric Surgery Case Reports

سال: 2018

ISSN: 2213-5766

DOI: 10.1016/j.epsc.2018.01.010