A Case of Congenital Laryngeal Atresia with Diaphragmatic Hernia / 대한주산의학회잡지
Korean Journal of Perinatology
;
: 185-190, 2010.
Artículo
en Coreano
| WPRIM
| ID: wpr-6945
ABSTRACT
Congenital laryngeal atresia is a rare cause of airway obstruction that is almost always lethal within short period of time after birth unless diagnosed prenatally and emergency tracheostomy was performed. Other life-threatening anomalies such as tracheoesophageal fistula, gastrointestinal or urinary anomalies, and VATER syndrome are often associated with laryngeal atresia. Recently, we experienced a case of congenital laryngeal atresia with diaphragmatic hernia, ear and skull anomalies, not diagnosed prenatally, died of asphyxia due to intubation failure, and confirmed by autopsy. We report this case with a brief review of the literatures.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Asfixia
/
Cráneo
/
Autopsia
/
Traqueostomía
/
Fístula Traqueoesofágica
/
Parto
/
Obstrucción de las Vías Aéreas
/
Oído
/
Urgencias Médicas
/
Hernia Diafragmática
Idioma:
Coreano
Revista:
Korean Journal of Perinatology
Año:
2010
Tipo del documento:
Artículo
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