Abstract
Tracheal agenesis is a rare but fatal congenital tracheal malformation. Lack of prenatal symptom and a typical clinical presentation lead to failure to arrive at a correct diagnosis and confusion during resuscitation. We report a case of a newborn male child with type 2 tracheal agenesis. Despite a typical presentation, diagnosis was delayed after unsuccessful intubation, examination under anaesthesia and emergency tracheostomy. The embryology, diagnostic criteria and potential treatment options are discussed. This case report is valuable in increasing awareness of this rare condition and will help us in being better prepared in managing these children. Future studies should aim to find the optimal replacement for the tracheal.
Reference18 articles.
1. Tracheal agenesis: approach towards this severe diagnosis. Case report and review of the literature;de Groot-van der Mooren;Eur J Pediatr,2012
2. Tracheal agenesis, a frightening scenario;Mohammed;J Laryngol Otol,2016
3. Congenital absence of the trachea;Payne;Brooklyn Med J,1900
4. Agenesis of the trachea;Floyd;Am Rev Respir Dis,1962
5. Embryogenesis of tracheo esophageal anomalies: a review;Merei;Pediatr Surg Int,2002
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