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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Lymphocytic interstitial pneumonitis in autoimmune thyroid disease
R Khardori1, L E Eagleton, N G Soler
1Department of Medicine, Southern Illinois University School of Medicine, Springfield 62794-9230.
The American Journal of Medicine
|May 1, 1991
Summary
Autoimmune thyroid disease may cause lymphocytic interstitial pneumonitis. This lung condition, a potential manifestation of immune dysfunction, responded to steroid therapy in four patients.
Area of Science:
- Immunology
- Pulmonology
- Endocrinology
Background:
- Autoimmune thyroid disease (AITD) encompasses conditions like Hashimoto's thyroiditis and Graves' disease, involving immune system attacks on the thyroid gland.
- Lymphocytic interstitial pneumonitis (LIP) is a rare lung disease characterized by the infiltration of lymphocytes into the lung interstitium, often idiopathic or associated with other conditions.
Observation:
- Four patients presented with concurrent autoimmune thyroid disease and lymphocytic interstitial pneumonitis.
- These patients were not on medications known to induce LIP.
- Clinical observations included a positive response to steroid treatment and symptom relapse upon steroid withdrawal.
Findings:
- The observed response to steroids and subsequent relapse suggest an underlying immunologic basis for LIP in these patients.
- This indicates that LIP may be a pulmonary manifestation of the immune dysregulation present in autoimmune thyroid disease.
Implications:
- The findings suggest a potential link between autoimmune thyroid disease and lymphocytic interstitial pneumonitis, expanding the known spectrum of AITD manifestations.
- This highlights the importance of considering autoimmune thyroid disease in patients diagnosed with idiopathic LIP and vice versa.
- Further research into the immunopathogenesis of this association could lead to novel therapeutic strategies for both conditions.
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