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导致气管食管受压的先天性血管异常。

Congenital vascular anomalies causing tracheoesophageal compression.

作者信息

Smith R J, Smith M C, Glossop L P, Bailey C M, Evans J N

出版信息

Arch Otolaryngol. 1984 Feb;110(2):82-7. doi: 10.1001/archotol.1984.00800280016006.

Abstract

Congenital vascular anomalies of the great vessels causing marked tracheoesophageal compression are rare. Notable symptoms usually manifest in the neonatal period and include stridor, repeated cyanotic attacks, recurrent pneumonia, and dysphagia. Although the diagnosis can often be made from barium swallow studies, the preoperative examination should nevertheless include an endoscopy. This is essential if the degree of tracheomalacia is to be adequately assessed and other tracheobronchial abnormalities are to be identified. Possible airway problems can then be anticipated, thus minimizing postoperative respiratory difficulties.

摘要

导致明显气管食管受压的大血管先天性血管异常较为罕见。显著症状通常在新生儿期出现,包括喘鸣、反复的青紫发作、反复肺炎和吞咽困难。虽然通常可通过吞咽钡剂造影检查做出诊断,但术前检查仍应包括内镜检查。如果要充分评估气管软化程度并识别其他气管支气管异常,这是必不可少的。这样就可以预见可能的气道问题,从而将术后呼吸困难降至最低。

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