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先天性气管支气管狭窄的新形态学分类。

A new morphologic classification of congenital tracheobronchial stenosis.

机构信息

The National Service for Severe Tracheal Disease in Children, The Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.

出版信息

Ann Thorac Surg. 2012 Mar;93(3):958-61. doi: 10.1016/j.athoracsur.2011.12.019.

Abstract

BACKGROUND

Congenital tracheal stenoses are rare and life-threatening anomalies, associated with considerable variation in both morphology and prognosis. They have been classified previously according to the length of the stenosis or the severity of the symptoms, but not according to bronchial involvement.

METHODS

Data from patients who underwent slide tracheoplasty for long-segment (>50%) congenital tracheal stenosis were collected. We identified four different types of bronchial arborization (normal, n=52; tracheal right upper lobe bronchus, n=10; carina with "trifurcation," n=14; and unilateral bronchial and lung agenesis, n=8). Each type included congenital tracheal (above the carina) or tracheobronchial (extending below the carina) stenosis.

RESULTS

Eighty-four children were enrolled in the study. Preoperative ventilation was necessary in 44 patients (52.4%; 75% in patients with a single lung), and preoperative extracorporeal membrane oxygenation was needed in 10 patients (11.9%). Preoperative tracheostomy was present in 3 patients initially treated elsewhere (3.5%), and a left pulmonary artery sling was performed in 44% (37 of 84). The overall mortality was 13% (11 of 84), 7.9% in patients with tracheal stenosis and 28.6% with tracheobronchial stenosis. No deaths occurred in patients with right upper lobe bronchus anatomy. Endoscopic procedures after slide tracheoplasty were required in 34 patients (40.4%). Stents were placed in 18 patients (21.4%), with a higher incidence in those with bronchial trifurcation (42.8%, 6 of 12).

CONCLUSIONS

This classification appears useful for the morphologic characterization of congenital airway stenosis and could be the benchmark for future prospective studies on the outcome of these patients.

摘要

背景

先天性气管狭窄是罕见且危及生命的异常,其形态和预后差异较大。先前根据狭窄长度或症状严重程度对其进行了分类,但未根据支气管受累情况进行分类。

方法

收集了接受滑式气管成形术治疗长段(>50%)先天性气管狭窄患者的数据。我们确定了四种不同类型的支气管分支(正常,n=52;气管右上叶支气管,n=10;隆突处“三分叉”,n=14;单侧支气管和肺缺如,n=8)。每种类型均包括先天性气管(隆突以上)或气管支气管(隆突以下)狭窄。

结果

本研究共纳入 84 名儿童。44 名患者(52.4%;单肺患者中 75%)需要术前通气,10 名患者(11.9%)需要术前体外膜氧合。3 名最初在其他地方治疗的患者(3.5%)存在术前气管造口术,44%(37 例/84 例)患者存在左肺动脉吊带。总体死亡率为 13%(84 例中的 11 例),气管狭窄患者为 7.9%,气管支气管狭窄患者为 28.6%。右上叶支气管解剖患者无一例死亡。滑式气管成形术后需要进行内镜处理的患者有 34 例(40.4%)。18 名患者(21.4%)放置了支架,其中支气管三分叉患者的发生率较高(42.8%,12 例中的 6 例)。

结论

这种分类方法似乎有助于先天性气道狭窄的形态学特征描述,可作为未来研究此类患者结局的基准。

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