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Updated: May 24, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Interstitial lung disease in the connective tissue diseases
Danielle Antin-Ozerkis1, Ami Rubinowitz, Janine Evans
1Yale Interstitial Lung Disease Program, Pulmonary & Critical Care Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510, USA. danielle.antin-ozerkis@yale.edu
Connective tissue diseases (CTDs) often cause interstitial lung disease (ILD), which can be the initial symptom. Early diagnosis and treatment with immunosuppressants are crucial for managing CTD-ILD.
Area of Science:
- Rheumatology
- Pulmonology
- Immunology
Background:
- Connective tissue diseases (CTDs) are inflammatory, immune-mediated disorders.
- Interstitial lung disease (ILD) is a common and significant complication of CTDs.
- ILD can be the initial clinical presentation of an underlying CTD.
Purpose of the Study:
- To highlight the importance of recognizing interstitial lung disease (ILD) in the context of connective tissue diseases (CTDs).
- To emphasize the diagnostic considerations and therapeutic approaches for CTD-associated ILD.
Main Methods:
- Literature review on CTD-associated ILD.
- Clinical presentation analysis of CTD-ILD.
- Diagnostic criteria and treatment strategies for CTD-ILD.
Main Results:
- Interstitial lung disease (ILD) is a frequent and critical manifestation of connective tissue diseases (CTDs).
- CTD-ILD often presents insidiously with cough and dyspnea, but can rarely manifest as acute respiratory failure.
- Exclusion of infection and drug reactions is essential; idiopathic ILD diagnosis requires ruling out underlying CTD.
Conclusions:
- A thorough investigation for underlying CTD is imperative before diagnosing idiopathic ILD.
- Treatment for CTD-associated ILD typically involves corticosteroids and immunosuppressive agents.
- Recognizing ILD as a potential early sign of CTD is vital for timely and appropriate patient management.
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