Abstract
From the authors: We would like to thank F. Kollert and co-workers for their interest in our article [1] and their accurate analysis and comments. Our study was designed to compare interstitial lung disease (ILD) in granulomatosis-associated common variable immunodeficiency disorder (CVID) (ILD/CVID/granulomatous disease) with pulmonary sarcoidosis. We found that lung manifestations in ILD/CVID/granulomatous disease were different from those in pulmonary sarcoidosis patients, taking into account their clinical history, physical examination, computed tomography (CT) imaging and bronchoalveolar lavage (BAL). Regarding CT imaging, the features in the cohort of F. Kollert and …
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