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Granulomatous-Lymphocytic Interstitial Lung Disease (GLILD) in Common Variable Immunodeficiency (CVID)

Granulomatous-Lymphocytic Interstitial Lung Disease (GLILD) in Common Variable Immunodeficiency (CVID)▶ Watch on YouTube — age-restricted, cannot embed here

Imaging findings

Chest x-ray shows extensive, bilateral, and diffuse lung disease, primarily in the lower lung zones, characterized by subsegmental, ill-defined opacities. CT demonstrates significant airway disease, including thickened bronchial walls and areas where small airways and bronchioles may contain material in their lumens. Expiratory imaging sequences reveal prominent air trapping, particularly in the upper lungs. The large opacities are speculated to be combinations of granulomatous findings and lymphocytes.

Key takeaways

Patients with Common Variable Immunodeficiency (CVID) are prone to developing Granulomatous-Lymphocytic Interstitial Lung Disease (GLILD). Imaging features of GLILD include a combination of airway disease (follicular bronchiolitis, bronchial wall thickening, mucostasis), ground-glass or consolidated opacities, and air trapping. The opacities can be due to lymphoid interstitial pneumonia (LIP) or granulomatous inflammation. Expiratory CT is important to detect air trapping secondary to bronchiolar obstruction.

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