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先天性长节段气管狭窄伴呼吸急促。

Congenital long segment tracheal stenosis presenting with tachypnea.

作者信息

Sheikh S, Nagaraj H S, Madden R

机构信息

Division of Pediatric Pulmonary Medicine.

出版信息

Paediatr Child Health. 2000 Jul;5(5):269-72. doi: 10.1093/pch/5.5.269.

Abstract

An infant born at full term presented with tachypnea, tachycardia and fatigue with feedings. Blood gases revealed hypoventilation. A rigid bronchoscopy using the Karl-Storz telescopic system revealed severe tracheal stenosis. Follow-up three-dimensional computerized tomography scans of the neck and chest revealed a long segment, funnel-shaped tracheal stenosis extending up to the left bronchial orifice. The patient underwent tracheal reconstruction, but died three weeks later from postoperative complications. It is unusual for severe tracheal stenosis to present without stridor, apnea, cyanosis and wheezing. Infants with unexplained tachypnea should be worked-up for congenital deformities of the upper airways.

摘要

一名足月儿出生后出现呼吸急促、心动过速及喂养时易疲劳。血气分析显示通气不足。使用卡尔史托斯(Karl-Storz)伸缩式系统进行的硬质支气管镜检查显示严重气管狭窄。颈部和胸部的后续三维计算机断层扫描显示,一段长节段、漏斗形气管狭窄向上延伸至左支气管开口处。该患者接受了气管重建手术,但三周后因术后并发症死亡。严重气管狭窄而无喘鸣、呼吸暂停、发绀和喘息并不常见。对于不明原因呼吸急促的婴儿,应检查是否存在上呼吸道先天性畸形。

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本文引用的文献

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