Share:
Peer-Reviewed Publication
Arch Soc Esp Oftalmol (Engl Ed)2026;101(5):502488.May 1, 2026Case Reports

Granulomatosis with polyangiitis. A diagnostic challenge in pediatric patients.

A M Blanco López1, A García Vázquez2
1Departamento de Oftalmología, Hospital Universitario Lucus Augusti, Lugo, Spain. Electronic address: ana.maria.blanco.lopez@sergas.es.
2Departamento de Oftalmología, Unidad de Oculoplástica y Órbita, Hospital Universitario Lucus Augusti, Lugo, Spain.

Abstract

Granulomatosis with polyangiitis is a systemic autoimmune disease characterized by the presence of granulomatous necrotizing vasculitis with kidney, respiratory, and vascular involvement, whose peak incidence is in the fifth and sixth decades of life. Its localized presentation without systemic involvement is infrequent. We present the case of a 10-year-old patient with recurrent eyelid edema as t…

Create a free account to keep reading

Free members get 10 full research views every month across publications, clinical trials, FDA clearances, adverse events, and NIH grants. No credit card required.

Want unlimited research access? See Pro plans

Data Accuracy Notice: Research intelligence on Health AI Central is aggregated from public sources (PubMed, ClinicalTrials.gov, FDA, NIH, CMS, and others) and refreshed nightly. Classifications and derived metrics are produced by automated methods described in our Methodology. We recommend verifying critical data points against the primary sources before making decisions.