A Case of Congenital Laryngeal Atresia with Diaphragmatic Hernia / 대한주산의학회잡지
Korean Journal of Perinatology
; : 185-190, 2010.
Article
em Ko
| WPRIM
| ID: wpr-6945
Biblioteca responsável:
WPRO
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.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Asfixia
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Crânio
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Autopsia
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Traqueostomia
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Fístula Traqueoesofágica
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Parto
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Obstrução das Vias Respiratórias
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Orelha
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Emergências
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Hérnia Diafragmática
Idioma:
Ko
Revista:
Korean Journal of Perinatology
Ano de publicação:
2010
Tipo de documento:
Article