retinal vasculitis/höfuðverkur

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Retinal vasculitis in Susac syndrome: case report.

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A 29 year old male was admitted at the emergency room suffering from gradually worsening headache followed by nausea. In the hospital patient presented with lethargy, reduction of consciousness level and bilateral hypoacusis. Ophthalmic examination and fluorescein angiography showed retinal

Peripheral capillary nonperfusion and full-field electroretinographic changes in eyes with frosted branch-like appearance retinal vasculitis.

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We report a patient with frosted branch-like appearance retinal vasculitis associated with peripheral capillary nonperfusion and full-field electroretinographic changes. A 62-year-old man presented with sudden bilateral decreased vision accompanied by headaches. His best-corrected visual acuity was

Ocular toxoplasmosis: a very rare presentation in an immunocompetent patient.

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A 28-year-old man presented with a 2-week history of red eye, photophobia, pain and decreased visual acuity of the right eye. The ophthalmological examination revealed hypertensive non-granulomatous panuveitis, retinal vasculitis with focus of retinochoroiditis with pigmented central area suggestive

[Ocular manifestations of syphilitic uveoretinitis in patients co-infected with human immunodeficiency virus].

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OBJECTIVE To investigate the clinical manifestations of syphilitic uveoretinitis in patients co-infected with human immunodeficiency virus (HIV). METHODS Uveoretinitis patients presenting between January 2008 and December 2014 at Eye and ENT Hospital of Fudan University were collected. Patients were

Coxsackievirus B3-associated panuveitis.

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A 29-year-old woman suffered from headaches, diarrhoea, and high grade fever followed by a unilateral retinal vasculitis, papillitis, and chorioretinitis. Abnormal electrocardiographic findings and antibody titre dynamics strongly suggested a coxsackievirus B3 infection. With respect to prior

Ocular syphilis: the new epidemic.

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OBJECTIVE To present the clinical presentation, diagnosis, and management of syphilitic uveitis in the context of an epidemic of syphilis in the UK. METHODS Retrospective clinical case series. RESULTS Six new cases of syphilitic uveitis presented to the Manchester Uveitis Clinic in 2004, after a

[Cerebral thrombophlebitis disclosing Behçet disease. Value of high resolution MRI].

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A 21-year-old male of Moroccan descent was admitted for inflammatory polyarthralgia and monoarthritis of the left knee. The patient reported a history of recurrent isolated aphthous ulcerations of the oral cavity. He was found to be positive for the HLA B5 antigen. The other investigations for

Cerebral venous thrombosis as the initial presentation of Behcet's disease.

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Neurological symptoms are rare manifestations of Behcet's disease. In this paper, we report cerebral venous thrombosis as the initial presentation of Behcet's disease in a 40 yearold man. Our patient presented with a six-week history of headache, progressive loss of vision in the right eye and

Adult Behcet's disease in Iran: analysis of 6075 patients.

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BACKGROUND This is an analysis of adult Behcet's disease (BD) in Iran, from the Iran Registry of 7187 BD patients, gathered from 1975 to 2014, among which 6075 were adults (84.5%). METHODS Patients were seen by a multidisciplinary team of experts. The diagnosis was by expert opinion, not by any

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