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Updated: Sep 17, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Expert consensus on interstitial lung disease associated with systemic autoimmune diseases. Executive summary
A González-García1, M Akasbi2, M P Brito-Zerón3
1Unidad de Enfermedades Autoinmunes Sistémicas, Servicio de Medicina Interna, Hospital Ramón y Cajal, IRYCIS. Carretera de Colmenar Viejo, Madrid, Spain.
Abstract:
Interstitial lung disease (ILD) is a frequent and potentially fatal manifestation of systemic autoimmune diseases (SAD). Early screening, diagnosis, and treatment with immunomodulators, and in some cases, antifibrotics, as well as appropriate follow-up, are essential to improving patients' quality of life and survival. The complexity of these diseases and the limited robust evidence to guide clinical decision-making lead to significant variability in management guidelines. In this article, a group of experts in SAD has developed recommendations for the screening, diagnosis, treatment, and follow-up of ILD, considering the latest evidence, their clinical experience, and the results of a survey conducted among specialists. The diseases included are systemic sclerosis, Sjögren's disease, idiopathic inflammatory myopathy, ANCA-associated vasculitis, sarcoidosis and systemic lupus erythematosus.
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