ReviewOphthalmology and therapy2019
Ocular Manifestations of Granulomatosis with Polyangiitis: A Review of the Literature.
Review in Ophthalmology and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.
What it found
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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.
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Who cites it
43 citing papers in PubMed, 102 citations in OpenAlex.
- Granulomatosis with polyangiitis-associated choroiditis simulating serpiginous choroiditis.American journal of ophthalmology case reports · 2026Article
- Isolated Bilateral Periocular Lupus Miliaris Disseminatus Faciei: A Clinicopathological Mimicker of Granulomatosis With Polyangiitis.The American journal of case reports · 2026Article
- A Red Eye in an Elderly Patient: A Case Report Highlighting the Importance of Urgent Diagnosis.Cureus · 2025Article
- Granulomatosis with Polyangiitis (GPA) in a Polish Tertiary Centre (2010-2025): Sex-Stratified Phenotypes, Serology, and Evolving Treatment Patterns.Journal of clinical medicine · 2025Article
- Granulomatosis with polyangiitis presenting as axial proptosis and corneal perforation-a case report.BMC ophthalmology · 2025Article
- Endoscopic vs. External Dacryocystorhinostomy in Granulomatosis with Polyangiitis: A Scoping Review of the Literature and Our Experience with Endoscopic Dacryocystorhinostomy.Journal of personalized medicine · 2025Review
- Bilateral corneoscleritis with retrocorneal plaque as the initial presentation of granulomatosis with polyangiitis.BMC ophthalmology · 2025Article
- Review of atypical optic neuritis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025Review
- Presumed granulomatosis with polyangiitis presenting with anterior scleritis and inflammatory ciliary body granuloma.Journal of ophthalmic inflammation and infection · 2025Article
- Article
- Granulomatosis With Polyangiitis (GPA) Presenting With Painless Scleritis and Ocular Hypertension: Case Report.Case reports in immunology · 2025Article
- Article
- Ocular Manifestation of Granulomatosis with Polyangiitis Presenting as Serous Retinal Detachment: A Case Report.Medicina (Kaunas, Lithuania) · 2024Article
- Bilateral Choroidal Detachments Associated with Perinuclear Anti-Neutrophil Cytoplasmic Antibodies (P-ANCA) - Associated Vasculitis.Ocular immunology and inflammation · 2024Article
- Granulomatosis with Polyangiitis Discovered Because of Repeated Upper Eyelid Swelling.Medicina (Kaunas, Lithuania) · 2024Article
- Retinal thickness and microvascular alterations observed by optical coherence tomography in antineutrophil cytoplasmic antibody-associated vasculitis: a cross-sectional study.Quantitative imaging in medicine and surgery · 2024Article
- Ocular manifestations of granulomatosis with polyangiitis: report from a tertiary eye care center.International ophthalmology · 2024Article
- Rheumatic diseases detected in patients presenting with uveitis.Northern clinics of Istanbul · 2024Article
- Granulomatosis with polyangiitis: clinical characteristics and updates in diagnosis.Frontiers in medicine · 2024Review
- Profile, Healthcare Resource Consumption and Related Costs in ANCA-Associated Vasculitis Patients: A Real-World Analysis in Italy.Advances in therapy · 2023Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Granulomatosis with polyangiitis (GPA) is a rare systemic autoimmune disease of unknown etiology that is characterized by granulomatous inflammation, tissue necrosis, and vasculitis in small- and medium-sized vessels. Ocular and orbital manifestations are common in almost half of patients with GPA, affecting every structure of the eye, from the eyelid and orbit to the retina, the choroid, and the optic nerve, with a wide range of severity. Since imaging findings are not always specific for the diagnosis of GPA, biopsy is useful to confirm the diagnosis. Regarding treatment, a localized pharmaceutical and surgical approach may be helpful to achieve remission, while immunosuppressive therapy, corticosteroids, and cyclosporine are also useful. In any case, multidisciplinary intervention is required to reduce the rates of relapse and morbidity in patients with GPA.
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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.