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Updated: Jul 30, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Case Report: Common variable immunodeficiency phenotype and granulomatous-lymphocytic interstitial lung disease with
María Soledad Caldirola1,2, Espantoso Daiana1, Andrea Cecilia Gomez Raccio1
1Servicio de Inmunología, Hospital de Niños "Dr. Ricardo Gutiérrez", Buenos Aires, Argentina.
Common variable immunodeficiency (CVID) patients can develop severe lung disease. This study details the first Argentinian patient with CVID and granulomatous-lymphocytic interstitial lung disease linked to SOCS1 gene variants.
Area of Science:
- Immunology
- Genetics
- Pulmonology
Background:
- Common variable immunodeficiency (CVID) is a primary immunodeficiency characterized by impaired antibody production and increased susceptibility to infections.
- Complications of CVID include autoimmunity, lymphoproliferation, enteropathy, and malignancies, with chronic lung disease being a major cause of mortality.
- Granulomatous-lymphocytic interstitial lung disease (GLILD) is a significant pulmonary manifestation in CVID patients.
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