Publication Date
1-1-2024
Journal
Frontiers in Pediatrics
DOI
10.3389/fped.2024.1417724
PMID
39359743
PMCID
PMC11445013
PubMedCentral® Posted Date
9-18-2024
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Keywords
CVID, granulomatous disease, hypogammaglobulinemia, sarcoidosis, GLILD, granulomatous lymphocytic interstitial lung disease
Abstract
Common variable immunodeficiency (CVID) can be complicated by granulomatous disease, often granulomatous lymphocytic interstitial lung disease (GLILD). Granulomatous interstitial nephritis represents an atypical presentation in pediatrics. Our patient is a previously healthy 13-year-old white male with a recent diagnosis of CVID. He presented with a rash and laboratory findings included pancytopenia (white blood cells 2.6 cells × 10
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Allergy and Immunology Commons, Immune System Diseases Commons, Medical Immunology Commons
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