Current Concepts of IRVAN Syndrome 6

نویسندگان

  • Miguel Paciuc-Beja
  • Daniela Santos-Cantu
  • Sergio Groman-Lupa
  • Hugo Quiroz-Mercado
چکیده

IRVAN syndrome is a rare disease characterized by retinal vasculitis, retinal aneurysms and neuroretinitis. Patients are usually asymptomatic at diagnosis but over time, proliferative changes, macular hard exudates, macular edema and retinal vascular occlusions can lead to severe vision loss. In this article we review the signs, symptoms, workup and treatment options of this disease.

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Unilateral idiopathic retinal vasculitis, aneurysms, and neuroretinitis syndrome (IRVAN) in a young female

PURPOSE To report a case of Idiopathic retinal vasculitis, arteriolar macroaneurysms, and neuroretinitis (IRVAN). syndrome in a young female. CASE REPORT A 21-year-old woman presented with unilateral visual acuity (VA) loss. Ophthalmological examination disclosed unilateral optic disc swelling, star-shaped macular exudation, multiple aneurysms surrounded by perivascular exudation, retinal vas...

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[Early treatment of idiopathic vasculitis, aneurysms and neuroretinitis (IRVAN). A case report].

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Idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome typically affects young, healthy individuals. Despite the dramatic fundus appearance seen in this syndrome, these patients are usually asymptomatic. The syndrome includes peculiar vascular abnormalities in the form of multiple aneurysmal dilatations seen along retinal arterioles and optic nerve-head arterioles, which ...

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تاریخ انتشار 2015