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免疫性系统性疾病中的亚临床肺泡炎。

Subclinical alveolitis in immunologic systemic disorders.

作者信息

Wallaert B

机构信息

Département de Pneumologie, Hôpital A Calmette, Lille, France.

出版信息

Lung. 1990;168 Suppl:974-83. doi: 10.1007/BF02718235.

Abstract

Subclinical alveolitis is a frequent finding in immunologic systemic disorders. However the significance of subclinical alveolar inflammation does not seem to be univocal and varies according to the disease. The fact that pulmonary involvement is rare during the course of extrathoracic granulomatosis like Crohn's disease or primary cirrhosis and that subclinical alveolitis is frequent suggests that alveolar inflammation may be the expression in the lung of a systemic immune disorder. In contrast subclinical alveolitis in collagen-vascular diseases, particularly progressive systemic sclerosis, is frequently associated with abnormalities of lung parenchyma as assessed by CT scan supporting the hypothesis that subclinical alveolitis is associated with development of ILD. Close follow-up of these patients is needed to better determine whether subclinical alveolitis precedes ILD and whether early detection of subclinical alveolitis in immunologic systemic disorders may identify those patients that are at risk for the development of ILD in the future.

摘要

亚临床肺泡炎在免疫性全身性疾病中很常见。然而,亚临床肺泡炎症的意义似乎并不明确,且因疾病而异。像克罗恩病或原发性胆汁性肝硬化等胸外肉芽肿病病程中肺部受累罕见,而亚临床肺泡炎却很常见,这一事实表明肺泡炎症可能是全身性免疫紊乱在肺部的表现。相比之下,胶原血管病尤其是进行性系统性硬化症中的亚临床肺泡炎,经CT扫描评估,常与肺实质异常相关,这支持了亚临床肺泡炎与间质性肺病(ILD)发展相关的假说。需要对这些患者进行密切随访,以更好地确定亚临床肺泡炎是否先于ILD出现,以及在免疫性全身性疾病中早期检测亚临床肺泡炎是否能识别出未来有发生ILD风险的患者。

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