Results 51 to 60 of about 7,403 (131)
Granulomatous anterior uveitis with hypopyon in quiescent ulcerative colitis
Journal of Clinical Ophthalmology and ResearchWe report a rare case of granulomatous anterior uveitis with hypopyon in a 31-year-old male with quiescent ulcerative colitis. Despite the absence of active gastrointestinal symptoms, the patient presented with acute visual loss and marked anterior ...
K. Harshitha +3 more
doaj +1 more source
ERDHEIM‐Chester Disease: Two Fatal Cases With Unusual Presentations
Clinical Case Reports, Volume 14, Issue 6, June 2026.Fluorodeoxyglucose positron emission tomography‐computed tomography (FDG PET‐CT) demonstrated markedly increased metabolic activity in serosal surfaces including pericardium, pleura, and renal fascia, as well as diffuse uptake along vascular walls, particularly the entire aorta.
Ribero‐Vargas Daniel Andres +2 more
wiley +1 more source
An Unusual Association: Takayasu’s Arteritis and Tubulointerstitial Nephritis and Uveitis Syndrome
European Journal of Case Reports in Internal Medicine, 2020 The coexistence of two immune-mediated diseases in the same patient is unusual. Takayasu’s arteritis (TA), which is a chronic granulomatous vasculitis, was discovered in a 47-year-old woman followed for tubulointerstitial nephritis and uveitis syndrome ...
Abir Derbel +3 more
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Brimonidine-induced uveitis: The inflammatory aftermath of treatment
Indian Journal of Ophthalmology. Case ReportsWe report a rare case of late onset brimonidine-associated granulomatous anterior uveitis in a patient with primary open angle glaucoma (POAG). A 57-year-old female presented with insidious onset blurring of vision, redness, glare, and pain in the right ...
Hitisha Mittal +4 more
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A 73‐Year‐Old Man With Several Years of Difficulty Climbing Stairs and Frequent Tripping
Annals of Clinical and Translational Neurology, Volume 13, Issue 5, Page 1078-1083, May 2026.ABSTRACT A 73‐year‐old man presented with progressive weakness and atrophy predominantly affecting the distal finger flexors and quadriceps muscles. Electrophysiological studies demonstrated mixed myogenic and neurogenic features. Muscle MRI showed inflammatory changes, and muscle biopsy revealed granulomatous myositis with histologic features ...
Mehmet Can Sari +3 more
wiley +1 more source
Patterns of uveitis at a tertiary referral center in Northeastern Iran
Journal of Ophthalmic & Vision Research, 2018 Purpose: To describe the demographic and clinical patterns of patients with uveitis referred to a tertiary center in northeastern Iran. Methods: This cross-sectional retrospective study included 235 patients with uveitis who had been referred to the ...
Seyedeh Maryam Hosseini +3 more
doaj +1 more source
A New Mutation in Blau Syndrome
Case Reports in Rheumatology, 2015 Blau syndrome is a rare, autosomal dominant, granulomatous autoinflammatory disease. The classic triad of the disease includes recurrent uveitis, granulomatous dermatitis, and symmetrical arthritis.
Cengiz Zeybek +4 more
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Human Pathology ReportsBlau syndrome is a rare, autosomal dominant or de novo mutation, granulomatous, auto-inflammatory disorder classically manifesting as a triad of polyarthritis, uveitis, and dermatitis. Rarely, this disease involves visceral sites such as the liver, lung,
Kelly M. Garrity +4 more
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Case Reports in Ophthalmology, 2015 We present here a case of a 9-year-old boy with bilateral anterior uveitis and an extremely elevated urinary β2-microglobulin level (25,400 μg/l). The normal range for urinary excretion of β2-microglobulin is 0-300 μg/l.
Kathryn L. Pepple +3 more
doaj +1 more source
Case Reports in Ophthalmological MedicineTattoo-associated uveitis is a rare inflammatory condition linked to tattooed skin, often presenting as bilateral anterior uveitis with complications such as macular edema and retinal vasculitis.
Sara Isabel Ospina Londoño +2 more
doaj +1 more source