Universidade Federal do Paraná - UFPR - Curitiba (PR) Brasil.
Disciplina de Pneumologia, Departamento de Medicina, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo (SP) Brasil.
J Bras Pneumol. 2024 Mar 22;50(1):e20230132. doi: 10.36416/1806-3756/e20230132. eCollection 2024.
Connective tissue disease-associated interstitial lung disease (CTD-ILD) represents a group of systemic autoimmune disorders characterized by immune-mediated organ dysfunction. Systemic sclerosis, rheumatoid arthritis, idiopathic inflammatory myositis, and Sjögren's syndrome are the most common CTDs that present with pulmonary involvement, as well as with interstitial pneumonia with autoimmune features. The frequency of CTD-ILD varies according to the type of CTD, but the overall incidence is 15%, causing an important impact on morbidity and mortality. The decision of which CTD patient should be investigated for ILD is unclear for many CTDs. Besides that, the clinical spectrum can range from asymptomatic findings on imaging to respiratory failure and death. A significant proportion of patients will present with a more severe and progressive disease, and, for those, immunosuppression with corticosteroids and cytotoxic medications are the mainstay of pharmacological treatment. In this review, we summarized the approach to diagnosis and treatment of CTD-ILD, highlighting recent advances in therapeutics for the various forms of CTD.
结缔组织病相关性间质性肺疾病(CTD-ILD)是一组以免疫介导的器官功能障碍为特征的系统性自身免疫性疾病。系统性硬化症、类风湿关节炎、特发性炎性肌病和干燥综合征是最常见的伴有肺受累和自身免疫特征性间质性肺炎的 CTD。CTD-ILD 的频率根据 CTD 的类型而有所不同,但总体发生率为 15%,对发病率和死亡率有重要影响。对于许多 CTD,哪些 CTD 患者应进行ILD 检查的决策并不明确。此外,其临床谱可从影像学上无症状发现到呼吸衰竭和死亡。相当一部分患者会出现更严重和进行性疾病,对于这些患者,免疫抑制治疗包括皮质类固醇和细胞毒性药物是药物治疗的主要方法。在这篇综述中,我们总结了 CTD-ILD 的诊断和治疗方法,强调了各种形式的 CTD 治疗的最新进展。