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PURPOSE to evaluate the efficacy of monoclonal anti-tumor necrosis factor alpha antibody infliximab in treatment of refractory Wegene's granulomatosis. Clinical manifestations of Wegener's granulomatosis at the time of infliximab initiation were: proptosis of both eyes due to progressive retrobulbar granulomas, visual impairment, optic disc edema,(More)
Necrotizing herpetic retinopathies are serious, usually rapidly progressive diseases of retina. Three well defined syndromes can be outlined: acute retinal necrosis, progressive outer retinal necrosis and CMV retinitis. Two cases of acute retinal necrosis, where the clinical picture was probably influenced by the corticosteroid use are described. The(More)
PURPOSE To assess the diagnostic yield of vitreous fluid analysis and the therapeutic effect of pars plana vitrectomy in patients with suspected intraocular inflammation. METHODS During 2004-2008, pars plana vitrectomy was performed in 89 patients (101 eyes) out of 1233 patients with uveitis. Vitreous specimens were analyzed by cytologic and(More)
The authors present the case of a female patient who, following complicated surgery, developed endogenous endophthalmitis. Based on the clinical picture and microscopic finding in the punctuate of the affected vitreous body the diagnosis of endogenous mycotic endophthalmitis was established. The treatment of the condition is based on a combination of local(More)
Acute retinal necrosis is a sight-threatening disease caused by the group of herpesviruses. The aim of this paper is to report a case of acute retinal necrosis following ocular trauma in a patient initially treated with vaso-active drugs and corticosteroids for presumed ocular ischemic syndrome. A 51-years-old otherwise healthy man, who suffered from sudden(More)
To present a possible coincidence of cytomegalovirus retinitis and intraocular lymphoma in a patient with systemic non-Hodgkin’s lymphoma. A 47-year-old woman presented with decreased visual acuity associated with white retinal lesions in both eyes. A history of pneumonia of unknown aetiology closely preceded the deterioration of vision. Five years(More)
PURPOSE To describe a case report of a 23-year-old patient with retinitis pigmentosa (RP) misdiagnosed as uveitis. METHODS A comprehensive eye examination including automated visual field assessment, contrast sensitivity, colour vision discrimination, ultrasound examination (US), spectral domain optical coherence tomography (SD-OCT) and full-field(More)
The authors presents a review of some findings on the basis of which it is possible to classify uveitis, retinitis and choroiditis already at the time of its onset, and in particular subsequently, as an autoimmune disease. They consider this review an adequate basis for immunosuppression therapy of uveitis at the very onset, although they do not analyze it(More)
AIM To evaluate the type of uveitis, the time of the duration between the first ocular signs and establishing of the diagnosis of multiple sclerosis (MS), effect of the treatment, and the final visual acuity (VA). METHODS In a retrospective study, medical records of 41 patients (82 eyes) from the total of 1267 patients with uveitis treated at the Center(More)