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Interstitial lung diseases (ILDs) constitute a group of both acute and chronic lung diseases that affect one or more of all the lung parenchymal components forming the interstitium such as bronchi, alveoli, connective tissue, and blood- and lymphatic vessels. Despite being rare diseases, the more than 200 different subtypes of ILDs represent a heterogeneous disease category with different clinical, radiological, and cyto-histological characteristics. ILDs typically manifest as inflammation, fibrosis, or a combination of both, which are the underlying causes for the patients' usual perceived symptoms as dry cough, dyspnea on exertion, and fatigue1....