RESUMEN

Idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) is a rare syndrome affecting the retinal and optic disc vasculature. Diffuse retinal ischemia, macular edema, and neovascularization may lead to bilateral vision loss. The authors report a case of a 36-year-old woman presenting with branch retinal artery occlusion (BRAO) in her right eye who was subsequently diagnosed with IRVAN syndrome. She was treated with panretinal photocoagulation for peripheral retinal ischemia and pars plana vitrectomy for vitreous hemorrhage. She later developed a BRAO in her left eye. This case demonstrates that BRAO may be a presenting feature of IRVAN syndrome. [Ophthalmic Surg Lasers Imaging Retina. 2017;48:948-951.].

Asunto(s)

Aneurisma/diagnóstico , Oclusión de la Arteria Retiniana/diagnóstico , Vasculitis Retiniana/diagnóstico , Vasos Retinianos/patología , Retinitis/diagnóstico , Adulto , Aneurisma/cirugía , Femenino , Angiografía con Fluoresceína , Humanos , Coagulación con Láser , Oclusión de la Arteria Retiniana/cirugía , Vasculitis Retiniana/cirugía , Retinitis/cirugía , Tomografía de Coherencia Óptica , Vitrectomía