CTICasesGranulomatous-lymphocytic interstitial lung disease (GLILD) in CVID
Imaging findings
CT scan of a patient with common variable immunodeficiency (CVID) shows diffuse bronchocentric nodules, splenomegaly, and consolidation with mild traction bronchiectasis, which resolved completely following treatment with sirolimus and prednisone.
Key takeaways
Granulomatous-lymphocytic interstitial lung disease (GLILD) is a clinicopathologic complication of CVID. It is characterized by lymphocytic infiltration and granulomatous inflammation, mimicking sarcoidosis, and is highly responsive to immunosuppressive therapy.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Pulmonary veno-occlusive disease (PVOD) in mixed connective tissue diseaseVascular
- Ascending aortic pseudoaneurysm secondary to sternal wound infectionIatrogenic
- Septal emboli and spinal discitis/osteomyelitis with paravertebral abscessInfection
- Excipient lung disease (talc granulomatosis)Exposure
- Disseminated Mycobacterium avium complex (MAC) in HIVInfection
- Excipient lung disease secondary to oral painkiller abuseExposure
- Pectus excavatum mimicking right middle/lower lobe pneumonia (pseudo-pneumonia)Artifact
- Invasive Klebsiella syndrome with hepatic abscesses and necrotizing pneumoniaInfection
See all cases from October 26, 2019 →