Interstitial Lung Diseases (ILDs) encompass over 200 pulmonary disorders, characterized by fibrotic and inflammatory changes in the lung interstitium.
ILDs can be idiopathic, or related to systemic diseases, environmental exposure, or drugs. They're classified into four categories: idiopathic interstitial pneumonias, ILDs associated with systemic diseases, granulomatous ILDs, and other ILDs.
Patients typically present with dyspnea and dry cough. Diagnosis involves clinical evaluation, pulmonary function tests, high-resolution CT, and sometimes lung biopsy.
Treatment varies depending on the specific ILD and its cause, but often involves corticosteroids and immunosuppressants.
Understanding ILDs is crucial for early detection and appropriate treatment, thereby improving patient outcomes.
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