Tracheomalacia Associated with Esophageal Atresia: A case report / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
;
: 643-647, 2006.
Article
Dans Coréen
| WPRIM
| ID: wpr-134271
ABSTRACT
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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Thorax
/
Trachée
/
Pontage cardiopulmonaire
/
Cartilage
/
Bruits respiratoires
/
Sténose pathologique
/
Dyspnée
/
Atrésie de l'oesophage
/
Trachéomalacie
Limites du sujet:
Humains
/
Bébé
/
Mâle
langue:
Coréen
Texte intégral:
The Korean Journal of Thoracic and Cardiovascular Surgery
Année:
2006
Type:
Article
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