• 대한기관식도과학회지
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• 제2권1호
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• pp.129-134
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• 1996

Acquired nonmalignant tracheoesophageal fistulas were formerly considered rare lesions, but they have been increasingly reported in the recent past. The pathognomonic complaints of this life-threatening lesion are strangulating sensations and frequent paroxysmal coughings occurring several seconds after the ingestion of liquids or solids. Until the past decade, this lesion was most often caused by infection, trauma, or esophageal diverticula. Complications caused by cuffed tracheal tubes are now becoming more widely noticed. Especially, tracheoesophageal fistula is one of the more unusual of these complications. Author reports two patients with tracheoesophageal fistula caused by cuffed tracheal tube.

• Journal of Chest Surgery
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• 제27권3호
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• pp.244-250
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• 1994

Early recognition, vigorous preoperative preparation, sophisticated supportive care, control of sepsis, and intensive care nursing have produced remarkably improved results in the management of esophageal atresia. Successful surgery for esophageal atresia and tracheoesophageal fistula was carried out recently. Two neonates with esophageal atresia and distal tracheoesophageal fistula were type C. Transpleural end-to-end repair was carried out after gastrostomy due to low birth weight in case I associated with ventricular septal defect. Case 2 underwent primary retropleural end-to-end repair. A simple one-layer anastomosis with the sutures passing through all layers of`the esophagus was performed in all cases.

• Advances in pediatric surgery
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• 제14권1호
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• pp.88-93
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• 2008

Esophageal atresia with double tracheoesophageal fistula is a very rare anomaly and is difficulty to diagnose preoperatively. We treated a full term baby with esophageal atresia with double tracheoesophageal fistula. At the first operation, only the distal tracheoesophageal fistula was identified and ligated. When the upper esophageal pouch was opened, intermittent air leakages in sequence with positive bagging were noticed. However, intraoperative bronchoscopy did not identify a fistula in the proximal pouch, and the operation was completed with end to end anastomosis of the esophagus. On the $7^{th}$ postoperative day, esophagography showed another tracheoesophageal fistula proximal to the esophageal anastomosis. A wire was placed in the fistula preoperatively under bronchoscopy. At the 2nd operation through the same thoracotomy incision the proximal fistula was identified and ligated. On the $12^{th}$ postoperative day, esophagography showed neither stricture nor leakage.

• Journal of Chest Surgery
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• 제32권3호
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• pp.322-325
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• 1999

선천성 호흡기 식도루가 성인에서 발견되는 경우는 매우 드물다. 선천성 호흡기 식도루는 수술하지 않으면 대부분 영아기에 사망하는데 간혹 H 모양의 호흡기 식도루가 생존하여 성인 연령에서 발견되기도 한다. 성인에서는 주로 반복되는 폐렴이나 기관지확장증 같은 만성 염증성 질환을 보여 우연히 진단되는 경우가 많다. 성인 연령까지 생존하는 호흡기 식도루는 대체로 좌우 주기관지 이하의 하부 호흡기에 연결된 기관지 식도루로 우리나라에서는 40예 정도 보고되어 있다. 그러나 상부 호흡기인 기관과 연결된 기관 식도루는 보고되어 있지 않다. 한일병원 흉부외과에서는 우리나라 최초로 성인 연령에서 발견된 선천성 기관 식도루 1예를 수술치험하였기에 보고하는 바이다.

• Journal of Chest Surgery
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• 제26권4호
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• pp.333-336
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• 1993

Esophageal atresia and tracheoesophageal fistula may occur as separate entities but usually occur in combination.The first report of esophageal atresia with tracheoesophageal fistula was done by Thomas Gibson in 1696.In1941, Haight and Towlseg performed the first successful primary repair,recently we were experienced a case of esophageal atresia with distal tracheoesophageal fistula in infant patient who presented the symptoms of dyspnea and vomiting.The operation was performed transpleurally through right 4th intercostal space.Patient tolerated all the operative procedure and recovered uneventflly.He was well-being without other problem.

• 대한후두음성언어의학회지
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• 제31권2호
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• pp.83-86
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• 2020

Patients with tracheoesophageal fistula show signs of aspiration, possibly leading to pneumonia, which could be fatal to bed-ridden patients. Tracheoesophageal fistula occurs as a complication of intubation, tracheostomy tube insertion and nasogastric tube insertion. Possible etiology is pressure and ischemic necrosis given by tracheostomy tube and nasogastric tube to trachea and esophagus; or in some cases, larynx and hypopharynx. Meanwhile, for repair of tracheoesophageal fistula, transcervical approach can be considered but takes relatively long operation time and is not appropriate for patients with underlying diseases. We report a case of tracheoesophageal fistula complicated several years after tracheostomy tube and nasogastric tube insertion who came to medical attention with signs of aspiration. Authors successfully performed repair of the fistula under laryngeal microsurgery approach without skin incision and dissection, and thereby report the experience with review of literature.

• Advances in pediatric surgery
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• 제17권1호
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• pp.88-92
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• 2011

The onset of hypertrophic pyloric stenosis in the postoperative course of esophageal atresia with tracheoesophageal fistula is rarely reported. The diagnosis could be delayed due to its mimicking symptoms of other postoperative complications including gastroesophageal reflux or anastomotic stricture. We present an infant who had surgery for esophageal atresia with tracheoesophageal fistula. He had never fed since birth. The infant presented with an increased amount of orogastric tube drainage and consistently distended gastric air on simple abdominal X-ray. Abdominal ultrasonography showed hypertrophic thick pyloric muscle. The diagnosis of pyloric stenosis was confirmed d is rarely reported. The diagnosis could be delayed due to its mimicking symptoms of other postoperative complications including gastroesophageal reflux or anastomotic stricture. We present an infant who had surgery for esophageal atresia with tracheoesophageal fistula. He had never fed. The infant presented with uring surgery, After pyloromyotomy, the patient's condition improved.

• Journal of Yeungnam Medical Science
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• 제2권1호
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• pp.253-258
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• 1985

H type의 기관식도루 특히 성인에서 발견된 경우는 아주 드물다. 최근 영남대학교 의과대학 흉부외과학교실에서는 식도폐쇄를 동반하지 않은 선천성 기관식도루 1예를 수술치험하여 양호한 성적을 얻었기에 문헌고찰과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제19권2호
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• pp.358-362
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• 1986

Esophageal atresia and tracheoesophageal fistula may occur as separate entities but usually occur in combination. Recently we were experienced a case of esophageal atresia with distal tracheoesophageal fistula in infant patient who presented the symptoms of projectile vomiting and dyspnea. The diagnosis was made by the esophagography and the Haight`s operation was performed transpleurally through 4th intercostal space after gastrostomy. Operative patient tolerated all the operative procedures well in spite of postoperative respiratory complication and recovered uneventfully, permitted feeding on 10th postoperative day. On follow up study after 5th months, Patient reveals good health without other problem.

• Journal of Chest Surgery
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• 제26권7호
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• pp.575-578
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• 1993

A tracheoesophageal fistula following blunt chest trauma is rare, with only slightly more than 40 cases having been reported since 1936. With the increased incidence of blunt chest trauma from traffic accidents, it may be anticipated that this complication will be seen more frequently in the future. This report describes successfully managed two cases with such lesion. The pathophysiology and management of such lesion are discussed with a review of the literatures.