• 대한기관식도과학회지
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• 제3권1호
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• pp.61-69
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• 1997

A total of 55 patients underwent surgical managements for postintubation tracheal stenosis from July 1975 through March 1997. All but 8 had received ventilatory assistance. The patients had S cuff lesions, 17 stoma lesions, 7 at both levels, 5 at subglottic lesions. Thirty two patients underwent the sleeve tracheal resection and end-to-end anastomosis. Five patients performed a wedge resection and end-to-end anastomosis. Twenty two patients received the Montgomery T-tube for relief of airway obstruction. Simple excision of granulation tissue was done in 7 patients. Rethi procedures(anterior division of cricoid cartilage, partial wedge resection of lower thyroid cartilage and T-tube molding) were performed in 2 subglottic stenosis patients. And the other subglottic patient was received permanent tracheal fenestration at 1975. The tracheoesophageal fistula patient was done sleeve tracheal resection and end-to-end anastomosis with interrupted double layer closure of esophageal fistula site. Cervical approach was used in 49 cases, cervicomediastinal in 13 cases and median stemotomy In 6 cases. Techniques for obtaining tension-free anastomosis included a cervical neck flexion(15-30$^{\circ}$) in all sleeve resection patients and laryngeal release in one. The length of resection was 1.5 to 5.0 on A total of 41 patients(74.5%) had good(24 patients) or satisfactory(17 patients) results. But in ten cases, the restenosis of anastomosis site which is the most common complication was developed Two of them underwent a second reconstruction and 8 patients required T-tube insertion for airway maintenance. Three patients(5.4%) died. The causes of death were tracheo-innominate artery fistula(2) and sudden obstruction of airway(1).

• Advances in pediatric surgery
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• 제17권1호
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• pp.81-87
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• 2011

This study was aimed to evaluate associated congenital anomalies in the patients with esophageal atresia with tracheoesophageal fistula (EA/TEF). Forty-two neonates with the diagnosis of EA/TEF treated over a 10 year period in a single institution were included in this study. The demography of EA/TEF was analyzed. Major associated anomalies including vertebral, anal, cardiac, renal, limb, neurologic and chromosome were reviewed and categorized. Males were slightly more dominant than females (1.47:1) and all patients had Gross type C EA/TEF. Only 19 % of the patients had solitary EA/TEF without associated anomalies. Cardiac anomalies were the most common associated congenital anomaly in patients with EA/TEF (73.8 %). But 47.6 % were cured spontaneously or did not affect patients' life. Atrial septal defect (ASD) was the most common cardiac anomaly followed by patent ductus arterious (PDA) and ventricular septal defect (VSD). Among gastrointestinal anomalies (23.8 %), anorectal malformations were the most frequent, 70 % Vertebral and limb abnormalities accounted for 11.9 % and urogenital malformations 9.5 % of the anomalies in patients with EA/TEF. VACTERL associated anomalies were 23.8 % and 1.8% had full VACTERL. Almost 12 % of EA/TEF had neurologic anomalies. Patients with EA/TEF require preoperative evaluation including neurologic evaluation to detect anomalies not related to VACTERL. Though associated cardiac anomaly occurred in 73.8 % of patients in our study, only 21.42 % needed surgical correction. The authors suggesrs further studies with large numbers of patients with EA/TEF.

• Journal of Chest Surgery
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• 제32권6호
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• pp.567-572
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• 1999

배경: 선천성 식도 폐쇄증의 수술적 교정은 많은 개선을 보였으나 아직도 사망률과 합병증률이 높은 상태이다. 방법: 1992년 1월부터 1997년 3월까지 본 동아대학교 병원 흉부외과학 교실에서는 27명의 선천성 식도 폐쇄증을 수술적 치료하였기에 이를 후향적으로 분석하고자 하였다. 결과: 남아가 21명 여아가 6명이었으며 평균 출생시 체중은 2.62$\pm$0.38 kg이었다. 원위부 기관식도루를 가진 식도폐쇄증이 24명이었고 나머지 3명은 순수 식도 폐쇄증이었다. Waterston의 위험군 분류상 A군이 4명, B군이 18명, C군이 5명이었다. 18명에서 동반 기형을 가졌으며 심혈관계 이상이 가장 흔한 동반 기형이었다. 식도 폐쇄증의 상하 식도 맹단 간의 거리는 1 cm이내의 short gap이 9명, 1내지 2 cm의 medium gap이 8명, 2 cm이상의 long gap이 7명, 3.5 cm 이상의 ultra-long gap이 3명이었다. 수술은 순수 식도 폐쇄증의 3례에서는 단계적으로 위루술 및 경부식도조루술을 시행하였고 나머지 24례는 모두 경흉강적 도달법으로 일시적 근치 교정술을 시행하였다. 추적기간 중 27명 중5명이 사망 하였는데 수술과 관련된 사망은 2명으로 그 중 1명은 급성 신부전으로 사망하였고, 1명은 문합부 누출로 인한 농흉 발생으로 사망하였다. 3명의 후기 사망이 있었는데 1명은 순수 식도 폐쇄증으로 식도-위-대장 문합술을 시행하였으나 인슐린 의존성 당뇨병으로 술후 29개월 째 사망하였고 1명은 동 괴사성장염(necrotizing enterocolitis)으로 사망, 나머지 1명은 \ulcorner선 확장술의 합병증으로 인해 술후 220일 째 십이지장 천공으로 인한 폐혈증으로 사망하였다 사망례의 분석을 통해 사망률에 영향을 미쳤던 요인들을 살펴 보았는데 gap length가 long gap이상일 경우가 사망률에 영향을 미치는 요소로서 통계적 유의성(p value<0.05)을 보였다. 결론: 수술적교정과 관련된 합병증률은 높은 편이나 이것이 수술사망률과 직결되는 것은 아니다. 전체적인 생존율은 효과적인 동반기형의 치료와 적극적인 수술후 관리가 병행될 때 더욱 향상시킬 수 있을 것이다.

• Journal of Chest Surgery
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• 제21권6호
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• pp.1084-1094
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• 1988

Conservative management of 3 iatrogenic perforations of intrathoracic esophagus was reviewed. The primary disorders were achalasia in 2 patients and congenital tracheoesophageal fistula in 1 patient. Perforation occurred after treatment of the primary disorders in the distal esophagus in 2 patients and mid-thoracic esophagus in 1 patient. All the perforations appeared late after the previous treatments and the inflammation spread to mediastinum and pleural cavity in all the 3 patients. Conservative management of esophageal perforation was carried out with intraluminal drainage from the perforated site of esophagus[insertion of Levin`s tube and continuous suction], pleural drainage and feeding of liquid diet through gastrostomy tube with Fowler`s position. The patients revealed spontaneous closure of perforated sites about 3 to 4 weeks after this conservative management without open thoracotomy. This result suggests that this conservative management may be accepted as therapeutic method in the thoracic esophageal perforations regardless of cause and time of the perforation.

• 대한기관식도과학회지
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• 제1권1호
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• pp.94-100
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• 1995

Despite improvement in respiratory care, including widespread use of low pressure and high volume cuffed tubes, tracheal stenosis remains a feared complication of prolonged intubation and tracheostomy. In such patients, other coexisting problems such as vocal cord paralysis, tracheoesophageal fistula, noncontiguous stenotic segments and laryngeal stenosis may occasionly be encountered. Therefore tracheal stenosis still presents a significant management problem, despite recent endoscopic advances and surgical techniques. Between 1991 and 1994, authors preformed tracheal resection with end-to-end anastomosis on 11 patients with tracheal stenosis. The total success rate (asymptomatic patients with patent airway) was 72.7% and there were no serious complication. This report reviews our experience about this procedure and surgical results. And it investigates associated factors for successful results.

• 대한기관식도과학회지
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• 제1권1호
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• pp.50-54
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• 1995

Despite improvement in respiratory care, including widespread use of low pressure and high volume cuffed tubes, tracheal stenosis remains a feared complication of prolonged intubation and tracheostomy. In such patients, other coexisting problems such as vocal cord paralysis, tracheoesophageal fistula, noncontiguous stenotic segments and laryngeal stenosis may occasionly be encountered. Therefore tracheal stenosis still presents a significant management problem, despite recent endoscopic advances and surgical techniques. Between 1991 and 1994, authors preformed tracheal resection with end-to-end anastomosis on 11 patients with tracheal stenosis. The total success rate (asymptomatic patients with patent airway) was 72.7% and there were no serious complication. This report reviews our experience about this procedure and surgical results. And it investigates associated factors for successful results.

• Journal of Chest Surgery
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• 제22권3호
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• pp.514-517
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• 1989

Congenital esophageal stenosis is a rare disease in childhood. By virtue of its complex embryological development, the esophagus is the site of many congenital abnormalities. Congenital Esophageal stenosis is one tenth as rare as tracheoesophageal fistula with esophageal atresia and is very rare in the cervical esophagus, which mostly occurred below mid-esophagus. Congenital esophageal web may be caused by the resorption failure of the epithelium following the vacuolization stage in embryonic development in the esophagus. Recently, we experienced 1 cases of congenital esophageal web, as the symptoms of life-long dysphagia. According to her history of dysphagia, radiologic and clinical findings, her esophageal stenosis was considered as congenital. For dilatation and relief of dysphagia, she underwent the Heineke-Mikulicz type of esophagoplasty. The results of surgical treatment were relatively good without any clinical events. So we reported it with its literature review.

• Advances in pediatric surgery
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• 제10권2호
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• pp.92-98
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• 2004

The history of esophageal replacement in infants or children is the history of development of various kinds of alternative conduits such as stomach, colon, and small bowel. The gastric tube has been the most widely used conduit. From January 1988 to May 2003, 23 esophageal replacements with gastric tube were performed at the Department of Pediatric Surgery, Seoul National University Childrens Hospital. Statistical analysis was performed using Windows SPSS11.0 Pearson exact test. There were Gross type A(n=10), type B(n=1), type C(n=11), type D(n=1). Ten patients who had long gap esophageal atresia (type A-8, type B-1, type C-1) and 13 patients (type A 2, type C-10, type D-1) who had stenosis, leakage, recurred tracheoesophageal fistula, and esophagocutaneous fistula after previous corrective operations, had esophageal replacement with gastric tube. Mean follow-up periods were 4 year 2 months (7 months-15 year 1 month). There were postoperative complications including GERD in 16 (69.6 %), leakages in 7 (30.4 %), diverticulum at anastomosis in 2 (8.7 %), anastomosis site stenosis in 4 (17.3 %), and distal stenosis of the gastric tube in 1 (4.3 %). There was no statistical significance between operation types and postoperative leakage and gastroesophageal reflux. In conclusion, esophageal replacement with gastric tube may be a useful surgical option in esophageal atresia with long gap and esophageal atresia complicated by previous corrective operation.

• 대한기관식도과학회지
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• 제14권1호
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• pp.59-64
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• 2008

Pure esophageal atresia without tracheoesophageal fistula is a uncommon form of congenital malformation of the esophagus, which is able to be suspected by fetal ultrasonograpy before delivery and diagnosed definitely by simple chest X-ray and esophagogram immidiately after delivery. We performed delayed primary repair in 2 cases of pure esophageal atresia by using stomach for conduit in one case and colon in the other case. But there were graft failure in the latter case, so reoperation was performed by using stomach. Postoperatively, two patients showed no stenosis and leakage in anastomotic site and were discharged in good oral intake without dysphagia.

• Advances in pediatric surgery
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• 제1권1호
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• pp.53-58
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• 1995

기관식도루를 동반하지 않은 원간격결손 식도폐쇄증 1예를 미리 조성한 위루와 경구를 통하여 주기적 부지를 함으로써 식도길이를 확장하여 식도-식도단단문합술로 식도의 개통복원을 할 수 있었음을 경험하였다. 이때 상부식도맹단부로부터 이중관을 이용한 지속적인 섬프배액술이 경과에 아주 긴요하며, 수술시 식도길이의 여유를 위하여 식도근환상절개술을 한 후에는 근절개부위의 협착 발생 가능성에 항상 주의하여 술 후 조기(술 후 2-4주)에 추시함이 꼭 필요하다고 생각하였다. 식도부지를 할 때에는 길이 뿐만 아니라 직경확장(특히 하부식도에서)에도 관심을 갖이면 더욱 좋은 결과를 얻을 수 있다고 판단된다.