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首页> 外文期刊>Paediatric anaesthesia >An unsuspected congenital laryngeal atresia with an associated tracheoesophageal fistula.
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An unsuspected congenital laryngeal atresia with an associated tracheoesophageal fistula.

机译:意外的先天性喉闭锁伴有气管食管瘘。

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摘要

Sir-A recent review evaluated the sonographic and magnetic resonance imaging (MRI) findings of trache-olaryngeal obstruction in the fetus describing the causes of obstruction and the management options (1). Fetal tracheolaryngeal obstruction is a life-threatening condition with substantial morbidity and mortality which is reported up to 80-100% when this condition is unrecognized before delivery (1). Congenital laryn-geal atresia (LA), resulting from the failure of larynx and trachea to canalize during embryogenesis, is one of the intrinsic causes of neonatal tracheolaryngeal obstruction. LA is a rare malformation characterized by a congenital high airway obstruction (2) and it can be diagnosed prenatally by ultrasonography identification of some peculiar signs of congenital high airway obstruction syndrome (CHAOS). Fetal MRI allows a more detailed definition of the level of the obstruction and the airways anatomy (1).
机译:Sir-A最近的一项评估评估了胎儿气管-喉管梗阻的超声和磁共振成像(MRI)发现,描述了梗阻的原因和治疗方案(1)。胎儿气管咽喉梗阻是一种危及生命的疾病,其发病率和死亡率均很高,据报道,在分娩前无法识别这种情况时,高达80-100%(1)。由于喉和气管在胚胎发生过程中无法进行导管形成而导致的先天性喉闭锁(LA)是新生儿气管咽喉梗阻的内在原因之一。 LA是一种罕见的畸形,其特征是先天性高气道阻塞(2),可以通过超声检查确定先天性高气道阻塞综合征(CHAOS)的某些特殊体征,从而对其进行诊断。胎儿MRI可以更详细地定义阻塞程度和气道解剖结构(1)。

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