Interstitial pneumonia with autoimmune features

Karjigi, Uma; Dharmanand, BG

doi:10.4103/0973-3698.332977

Cited by 2 publications

(1 citation statement)

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“…Up to 25% of patients with symptoms and signs concerning for an autoimmune disease do not meet the classification criteria for connective tissue disease (CTD) as per the American College of Rheumatology, and up to 20% of patients with idiopathic interstitial pneumonias have symptoms and clinical findings suggestive of underlying systemic processes ( 31 ). In 2015, the European Respiratory Society/American Thoracic Society developed a task force for “Undifferentiated Forms of CTD-associated ILD” and proposed a research classification of idiopathic pneumonia with autoimmune features (IPAF) to help guide further understanding of these patients ( 32 ).…”

Section: Interstitial Lung Diseasementioning

confidence: 99%

Myositis interstitial lung disease and autoantibodies

Chaudhry

Christopher‐Stine

2023

Front. Med.

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The aim of this review is to examine and evaluate published literature associated with idiopathic inflammatory myopathies (IIM) and interstitial lung disease (ILD) based on myositis specific autoantibodies (MSA) and the potential clinical significance of each autoantibody subtype for the practicing clinician. The review is a comprehensive search of literature published in PubMed from the year 2005 and onward coinciding with the surge in the discovery of new MSAs. Additionally, we comment on recommended multidisciplinary longitudinal care practices for patients with IIM-ILD with regard to imaging and other testing. Treatment is not covered in this review.

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Section: Interstitial Lung Diseasementioning

confidence: 99%