Tracheomalacia Associated with Esophageal Atresia: A case report / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
; : 643-647, 2006.
Article
在 Ko
| WPRIM
| ID: wpr-134271
Responsible library:
WPRO
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.
Key words
全文:
1
索引:
WPRIM
主要主题:
Thorax
/
Trachea
/
Cardiopulmonary Bypass
/
Cartilage
/
Respiratory Sounds
/
Constriction, Pathologic
/
Dyspnea
/
Esophageal Atresia
/
Tracheomalacia
限制:
Humans
/
Infant
/
Male
语言:
Ko
期刊:
The Korean Journal of Thoracic and Cardiovascular Surgery
年:
2006
类型:
Article