ArticleCureus2025
Infectious Scleritis Masquerading as Isolated Orbital Cellulitis: A Case Report.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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.
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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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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A woman in her fifties was presented to the emergency room with eye pain, swelling, redness, and reduced vision. The examination revealed periorbital swelling, limited extraocular motility, tenderness, and conjunctival chemosis, with thinning observed nasally at the site of prior pterygium repair. The anterior chamber was quiet, and B-scan (ultrasonography) revealed retino-choroidal thickening. Computed tomography (CT) scan results indicated septal cellulitis with clear sinuses. Laboratory workups were negative. The patient was diagnosed with orbital cellulitis and was admitted and treated accordingly. However, the patient developed recurrent attacks with hypopyon, which prompted another course of management. The patient was presented again, displaying an aggressive clinical picture, and there was a focal calcified plaque over the nasal area, suggesting necrotizing scleritis. B-scan shows T-sign and conjunctival recession, scleral scraping, debridement, and subconjunctival antibiotic injection were performed. A positive culture for Pseudomonas aeruginosa was identified. An agreement on the management of this ocular condition lacks a clear guideline. However, most infectious scleritis cases mandate a combined approach involving medical treatment and surgical debridement.
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Registered trials
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