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. 2019 Nov 20;134(21):1787–1795. doi: 10.1182/blood.2019002062

Figure 2.

Figure 2.

The patient in clinical case 2 had a slow decline in lung function due to his immune defect, but this was assumed to be due to sarcoidosis. Chest computed tomography showed ground-glass opacities with numerous nodules, hilar lymphadenopathy, and bronchiectatic changes. With granuloma on biopsy, these changes were consistent with granulomatous lymphocytic interstitial lung disease.