ArticleCureus2025
Eosinophilic Granulomatosis With Polyangiitis Presenting as Bilateral Orbital Inflammation.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Unilateral orbital mass as the initial presentation of pediatric antineutrophil cytoplasmic antibody associated vasculitis: eosinophilic granulomatosis with polyangiitis versus granulomatosis with polyangiitis.Journal of ophthalmic inflammation and infection · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Eosinophilic granulomatosis with polyangiitis (EGPA) is a small vessel vasculitis that most commonly presents with peripheral eosinophilia, upper airway disease, and asthma, and can also cause cutaneous, cardiac, neurologic, musculoskeletal, gastrointestinal, and renal disease. This case describes a 57-year-old male with a history of chronic sinusitis and asthma who presented with bilateral orbital inflammation causing proptosis and diplopia. He was initially treated with antibiotics for orbital cellulitis without benefit, then high-dose prednisone with taper for idiopathic orbital inflammation, with resolution of ocular symptoms. He was diagnosed with EGPA after rheumatologic evaluation. Serum Immunoglobulin G4 (IgG4) level was significantly elevated, but his clinical presentation was more consistent with EGPA than IgG4-related disease (IgG4-RD). The patient significantly improved with the addition of mepolizumab and later methotrexate. This case details a rare manifestation of EGPA-bilateral orbital inflammation and highlights the potential overlapping features between EGPA and IgG4-RD.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.