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Congenital high airway obstruction syndrome-antenatal diagnosis of a rare case of airway obstruction using multimodality imaging

机译:先天性高气道阻塞综合征-使用多模态成像对罕见的气道阻塞病例进行产前诊断

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摘要

Congenital high airway obstruction syndrome (CHAOS) is a rare condition which occurs as a result of congenital foetal airway obstruction which may be complete or partial. The disease is usually incompatible with life and leads to stillbirth or death shortly after delivery. However, due to advances in antenatal imaging by ultrasound and magnetic resonance imaging (MRI), more cases are being detected in the antenatal period. Commonly, CHAOS occur secondary to atresia or stenosis of the larynx or trachea, which may be partial or complete or due to a laryngeal cyst. We report a case of CHAOS due to laryn-geal atresia diagnosed by antenatal ultrasonography and foetal MRI. We also briefly review the pertinent literature.
机译:先天性高气道阻塞综合征(CHAOS)是一种罕见的疾病,是由于先天性胎儿气道梗阻(可能是完全的或部分的)而导致的。该疾病通常与生命不相容,并在分娩后不久导致死产或死亡。但是,由于通过超声和​​磁共振成像(MRI)进行产前成像的进步,在产前期发现了更多病例。通常,CHAOS继发于喉部或气管的闭锁或狭窄,继发于喉部或气管的一部分或全部,或由于喉囊肿。我们报告一例因产前超声检查和胎儿MRI诊断出的喉at闭锁而导致的CHAOS病例。我们还简要回顾了相关文献。

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