Tracheomalacia Associated with Esophageal Atresia: A case report / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
;
: 643-647, 2006.
Artículo
en Coreano
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Tórax
/
Tráquea
/
Puente Cardiopulmonar
/
Cartílago
/
Ruidos Respiratorios
/
Constricción Patológica
/
Disnea
/
Atresia Esofágica
/
Traqueomalacia
Límite:
Humanos
/
Lactante
/
Masculino
Idioma:
Coreano
Revista:
The Korean Journal of Thoracic and Cardiovascular Surgery
Año:
2006
Tipo del documento:
Artículo
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