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薄层计算机断层扫描表现对纤维化肺泡炎的预测价值。

The predictive value of appearances on thin-section computed tomography in fibrosing alveolitis.

作者信息

Wells A U, Hansell D M, Rubens M B, Cullinan P, Black C M, du Bois R M

机构信息

Interstitial Lung Disease Unit, Royal Brompton National Heart and Lung Hospital, London, United Kingdom.

出版信息

Am Rev Respir Dis. 1993 Oct;148(4 Pt 1):1076-82. doi: 10.1164/ajrccm/148.4_Pt_1.1076.

Abstract

Fibrosing alveolitis, a condition characterized by a poor prognosis and a limited response to treatment, is readily identified by thin-section computed tomography (CT). Fibrotic and inflammatory histologic results, obtained at open lung biopsy, both have characteristic CT patterns. To evaluate whether CT could predict prognosis and response to therapy, we examined the CT appearances of 76 patients with lone cryptogenic fibrosing alveolitis and 66 patients with fibrosing alveolitis associated with systemic sclerosis. CT abnormalities were categorized as predominantly a ground-glass pattern (Grade 1), mixed (Grade 2), or predominantly a reticular pattern (Grade 3). In cryptogenic fibrosing alveolitis, 4-yr survival was highest in association with CT Grade 1 and higher with CT Grade 2 than with CT Grade 3, independent of the extent of abnormal lung on CT, duration of dyspnea, or severity of depression of DLCO or FVC, p < 0.001. A response to therapy in previously untreated cryptogenic fibrosing alveolitis was seen most frequently with CT Grade 1 and more frequently with CT Grade 2 than with CT Grade 3, p < 0.025. In systemic sclerosis, CT appearances were not predictive of 4-yr survival; a response to therapy was seen more frequently with CT Grade 2 (three of seven patients) than with CT Grade 3 (zero of six patients). These data have shown that CT appearances are of prognostic value in fibrosing alveolitis and that they are likely to play an increasing role in disease-staging in this condition.

摘要

纤维化肺泡炎是一种预后较差且治疗反应有限的疾病,通过薄层计算机断层扫描(CT)很容易识别。在开胸肺活检中获得的纤维化和炎症组织学结果都有其特征性的CT表现。为了评估CT是否能够预测预后和对治疗的反应,我们检查了76例特发性隐源性纤维化肺泡炎患者和66例与系统性硬化症相关的纤维化肺泡炎患者的CT表现。CT异常主要分为磨玻璃样改变为主(1级)、混合性(2级)或网状改变为主(3级)。在隐源性纤维化肺泡炎中,4年生存率在CT 1级时最高,CT 2级高于CT 3级,与CT上肺部异常范围、呼吸困难持续时间或DLCO或FVC降低的严重程度无关,p<0.001。在先前未经治疗的隐源性纤维化肺泡炎中,对治疗有反应最常见于CT 1级,CT 2级比CT 3级更常见,p<0.025。在系统性硬化症中,CT表现不能预测4年生存率;对治疗有反应在CT 2级(7例患者中的3例)比CT 3级(6例患者中的0例)更常见。这些数据表明,CT表现对纤维化肺泡炎具有预后价值,并且它们可能在这种疾病的分期中发挥越来越重要的作用。

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