[肺间质性疾病和结缔组织疾病]。

S. Guler, T. Geiser
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引用次数: 0

摘要

风湿病的肺部受累具有广泛的临床和影像学表现,从急性炎症到慢性纤维化为主。对于预后和治疗考虑,需要详细的检查和最佳的多学科评估,也要排除肺部恶化的其他原因,如感染(免疫抑制治疗)或肺动脉高压。对于治疗指导,需要考虑几个方面,如疾病严重程度、疾病活动性、临床和放射学表现、预后标志物和合并症。免疫抑制治疗根据风湿病诊断的类型不同而不同,尽管在与风湿病相关的ILD中,最佳治疗的证据很少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Interstitial lung disease and connective tissue diseases].
Lung involvement in rheumatologic diseases has a broad spectrum of clinical and radiological presentations, from acute inflammatory to chronic, fibrosing predominance. For prognostic and therapeutic considerations a detailled work-up 'and optimally multidisciplinary evalution is needed, also to rule out other reasons for pulmonary deterioration such as infection (under immunosuppressive treatment) or pulmonary hypertension. For treatment guidance, several aspects need to be taken into consideration, such as disease severity, disease activity, clinical and radiological presentation, prognostic markers and comorbidities. Immunosuppressive treatment differs based on the type of rheumatologic diagnosis, although evidence for optimal therapy is rare in ILD associated with rheumatologic diseases.
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