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无名动脉对气管的压迫:一名12岁男孩呼吸暂停的罕见原因。

Innominate artery compression of the trachea: an unusual cause of apnea in a 12-year-old boy.

作者信息

Friedman Elliott, Kennedy Alana, Neitzschman Harold R

机构信息

Department of Radiology, Tulane University Health Sciences Center, New Orleans, LA 70112-2699, USA.

出版信息

South Med J. 2003 Nov;96(11):1161-4. doi: 10.1097/01.SMJ.0000072420.60411.9F.

Abstract

Innominate artery compression of the trachea is a common cause of airway obstruction in infants and young children. The clinical significance of this lesion, even when compression is documented endoscopically or radiographically, is controversial. Obstructive respiratory symptoms occur in only a fraction of such cases, and symptomatic patients are most commonly detected in the first year of life. We present a case of a 12-year-old boy with a chief complaint of progressive stridor and apnea who was diagnosed with symptomatic innominate artery compression of the trachea. We reviewed the literature regarding the pathology, diagnosis, and treatment of this condition.

摘要

无名动脉对气管的压迫是婴幼儿气道梗阻的常见原因。即使在内镜检查或影像学检查中证实存在压迫,这种病变的临床意义仍存在争议。只有一小部分此类病例会出现阻塞性呼吸症状,有症状的患者最常在出生后第一年被发现。我们报告一例12岁男孩,主要症状为进行性喘鸣和呼吸暂停,被诊断为有症状的无名动脉对气管的压迫。我们回顾了关于这种疾病的病理、诊断和治疗的文献。

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