• Title/Summary/Keyword: 식도 협착

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Congenital Esophageal Stenosis due to Tracheobronchial Remnants -1 case report- (기관기관지 잔유조직에 의한 선천성 식도협착 -1례 보고-)

  • 이선희;권종범
    • Journal of Chest Surgery
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    • v.29 no.2
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    • pp.248-250
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    • 1996

  • Congenital esophageal stenosis due to tracheobronchial remnant is very rare disease entity and usually occurs in mid and lower esophagus. The cause is esophageal sequestration of a tracheobronchial anlage before embryologic separation. A 4 years old girl was admitted with swallowing difficulty, food regurgitation which progressively got worse in recent 2 years. She was operated under the dagnosis of achalasia. During the myoto y procedure we found the bean sized hard nodular mass, which was 4cm above the esophagogastric junction, and after the resection of mass, esophagoplasty was carried out. The histologic finding of the mass revealed traheal cartilages and respiratory glands.

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Tracheomalacia Associated with Esophageal Atresia - A case report - (식도폐쇄증과 동반된 기관연화증 - 1예 보고 -)

  • Song Seung-Hwan;Chang Yun-Hee;Lee Chang-Hun;Shin Dong-Hoon;Sung Si-Chan
    • Journal of Chest Surgery
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    • v.39 no.8 s.265
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    • pp.643-647
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    • 2006

  • Congenital tracheomalacia associated esophageal atresia is a rare foregut anomaly. We report a case of 40-day old male infant with tracheomalacia who has undergone repair of esophageal atresia at his age of 1 day. The patient had progressive dyspnea and stridor after repair of esophageal atresia. His 3-dimensional chest computed tomography showed severe stenosis at the middle of trachea. We underwent resection and end-to-end anastomosis under cardiopulmonary bypass. Histologic examination revealed esophageal tissues indicating congenital origin as well as no cartilage.

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