• Journal of Chest Surgery
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• 제53권3호
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• pp.144-146
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• 2020

Supravalvar aortic stenosis (SVAS) is a rare congenital cardiac disease that usually co-occurs with Williams syndrome. In the adult population, a few SVAS cases have been reported in patients affected by homozygous familial hypercholesterolemia. However, because of the rarity of this disease entity, there is no standard surgical treatment for SVAS. Here, we present a case of successful surgical treatment using an autologous excised aortic patch in a 65-year-old patient with SVAS.

• Journal of Chest Surgery
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• 제48권5호
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• pp.351-354
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• 2015

A five-month-old boy who had undergone previously transcatheter balloon atrioseptostomy at 3 days of age for complete transposition of the great arteries with ventricular septal defect and pulmonary stenosis underwent pulmonary root translocation with the Lecompte maneuver. This operation has the advantages of maintaining pulmonary valve function, preserving the capacity for growth, and avoiding problems inherent to the right ventricular to pulmonary artery conduit. This patient progressed well for 9 months postoperatively and we report this case of pulmonary root translocation with the Lecompte maneuver.

• Journal of Chest Surgery
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• 제42권1호
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• pp.63-71
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• 2009

배경: 기관 협착의 치료방법은 비교적 덜 침습적인 기관지내시경을 이용한 시술 또는 침습적인 방법인 구역절제술과 문합의 방법이 있으나 가끔은 환자의 임상적 특징에 따라 이 모든 방법이 불가능할 때도 있다. 최근 실리콘 T-튜브 스텐트가 안전한 치료 대안이 되고 있다. 우리는 다양한 기저질환을 가진 기관 협착 환자에서 T-튜브의 중단기 결과를 조사하였다. 대상 및 방법: 1997년 1월부터 2007년 4월까지 10년 동안 T-튜브로 기관협착을 치료받은 환자 57명을 후향적으로 검토하였다. 환자의 의무기록과 영상검사를 기초로 하여, 임상적인 결과와 T-튜브 제거유무를 조사하였다. 결과: T-튜브와 연관된 합병증과 사망은 없었다. 경과 관찰 기간 동안 1명의 환자는 협착부위 절제와 재건술을 받았다. 13명의 환자들(13/57, 22.8%)은 성공적으로 T-튜브를 제거하여 더 이상 다른 처치는 필요하지 않았다. 또 다른 4명의 환자는 기관연화와 기관협착의 재발로 T-튜브 제거 후 다시 삽입하였다. 4명의 환자들은 기저질환과 암으로 사망하였다. 성별과 T-튜브 삽입 전 기관절개술 유무는 T-튜브 제거에 상당한 영향을 미치나 다변량 분석에서는 성별만이 T-튜브 제거 성공의 표지자로 밝혀졌다. 성별 (p=0.033)과 이전의 기관절개술(p=0.036)은 T-튜브 제거 성공군과 실패군 간의 2가지 다른 요소였다. 결론: T-튜브는 여러 원인에 의해 유발된 기관 협착에서도 믿을 만한 기도유지를 제공하였다. T-튜브는 중단기 동안 기관협착의 치료에 안전하고 효과적인 방법이라고 생각된다.

• Journal of Chest Surgery
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• 제38권11호
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• pp.795-798
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• 2005

기관 삽관 후에 발생한 기관 협착에 대한 근본적 치료는 기관 부분 절제 및 단단 문합이다. 기관 협착에 대한 성공적이지 못한 교정으로 인해 발생하는 기관의 재협착에 대한 수술 치료는 쉽지 않다. 재수술이 실패할 경우 환자는 평생 기관절개 상태 및 목소리 소실을 안고 살아야 한다. 첫 번째 수술이 실패했을 경우 염증반응, 부종, 섬유화가 해소될 때까지 약 $4\~6$개월을 기다린 후 재수술을 시행해야 한다 환자의 상태에 대한 정확한 평가가 필요하며 일단 재수술의 후보자로 선정되면 재수술의 성공률은 $90\%$ 이상이다. 저자들은 기관 삽관으로 인해 발생한 기관 협착에 대해 성공적이지 못한 교정 후 발생한 기관의 재협착 2예에 대한 치험을 문헌 고찰과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제28권10호
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• pp.939-941
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• 1995

Congenital esophageal stenosis due to tracheobronchial remnants is one of main forms of congenital esophageal stenosis.A 19-month-old male was presented an appearence of underdevelopment and mild dehydration state due to persistent vomiting since 5 months after his birth. Esophagogram revealed an abrupt narrowing of lower esophagus with dilatation above it. The operation method was aesection of esohageal stenosis and end to end anastomosis through left seventh thoracotomy. The postoperative course was uneventful.

• Journal of Chest Surgery
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• 제22권4호
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• pp.672-676
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• 1989

We experienced a case of congenital tricuspid stenosis. The patient was 5 years old boy. The 2D-echo 4 cardiac catheterization with cineangiogram revealed as Tricuspid Stenosis, associated with functioning patent foramen ovale & mild R.V hypoplasia. The lesion was successfully corrected by TV commissurotomy & closure of PFO. Postoperatively, moderate degree of tricuspid regurgitation was remained.

• Journal of Chest Surgery
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• 제25권10호
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• pp.1061-1065
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• 1992

There are more patients with tracheal stenosis lately due to the increased use of tracheostomy and assisted ventilation. Recently we have experienced two cases of post tracheostomy tracheal stenosis and successfully performed circumferential resection and end-to-end anastomosis of the trachea. Postoperative tracheostomy was not performed. The postoperative courses were uneventful and they are now conducting an usual life.

• Journal of Chest Surgery
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• 제18권2호
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• pp.345-351
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• 1985

Tracheal stenosis is due to tracheostomy or prolonged intubation. Development of tracheal stenosis following tracheostomy is very serious complication. In recent practice, tracheostomy has became more popular because of increased occasions of major and minor traumas. At the Dept. of thoracic surgery, Chonbuk national university hospital, we have experienced one case of tracheal stenosis following tracheostomy for assisted ventilation. Chest X-ray revealed the narrowing of trachea at cervicothoracic junction due to previous tracheostomy. We resected the narrow segment & tracheal reconstruction was performed with an excellent result in postoperative periods. Postoperative air tracheogram did not reveal demonstrable narrowing of air filled trachea.

• Journal of Chest Surgery
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• 제28권10호
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• pp.932-934
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• 1995

Esophageal stenosis due to ectopic tracheobronchial remnants is an uncommon anomaly and only few cases were reported in the literature. We have experienced two case of esophageal stenosis due to ectopic tracheobronchial remnants and performed operative correction. The one patient was a five year old male with a chief complaint of swallowing difficulty from birth and the other was a twenty-three year old female with a slowly incresing symptom of dysphagia for twenty years. both of them were performed surgical correction by esophagectomy of the stenotic portion and esophago-gastrostomy with anti-reflux procedures. The resected specimens of the these two patients showed ectopic tracheobronchial chondroepithelial tissue withinthe esophageal wall histipathologically. Postoperative course was uneventful and have been in good condition without any problems.

• Journal of Chest Surgery
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• 제19권2호
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• pp.313-318
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• 1986

A rare anomaly, Cor triatriatum dexter combined with pulmonary stenosis and patent foramen ovale in a 2-years- old female is presented. Abnormal embryologic development of the right sinus venosus valve caused partial membranous septation of the right atrium. Most cases have been recorded at necropsy either as an incidental finding or in association with severe congenital heart disease. In this case, Cor triatriatum dexter was diagnosed preoperatively by cineangiography and echocardiography.