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http://dx.doi.org/10.1016/j.jfo.2020.07.007 | DOI Listing |
Retin Cases Brief Rep
October 2024
Department of Ophthalmology, University of Sao Paulo, Sao Paulo, Brazil.
Purpose: To describe a multimodal imaging and a 5-year follow-up of a case of cilioretinal artery occlusion (CLRAO) in a 40-year-old woman with idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome.
Methods: Fundus photography, indocyanine green and fluorescein angiography, optical coherence tomography (OCT), OCT angiography (OCTA), and a literature review of retinal artery occlusions associated with IRVAN syndrome were performed.
Results: Fundus examination revealed bilateral blurred margins of the discs and peri-vascular hard exudates.
Medicine (Baltimore)
September 2024
Department of Ophthalmology, China Medical University Hospital, China Medical University, Taichung, Taiwan.
Rationale: The prevalence of idiopathic retinitis, vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome is <1/1,000,000, and it tends to occur in young women. Panretinal photocoagulation, focal laser photocoagulation, peripheral cryopexy, vitrectomy, and corticosteroid therapy are the traditional treatments. We reported a case of a senile patient with IRVAN syndrome who presented with severe exudation in both eyes and macular edema in the left eye, successfully treated by serial intravitreal aflibercept injections.
View Article and Find Full Text PDFOphthalmologie
September 2024
Smile Eyes Augen + Laserzentrum Leipzig, Lampestr. 1, 04107, Leipzig, Deutschland.
Cureus
April 2023
Ophthalmology, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, USA.
We report a case of idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome in a patient whose cystoid macular edema (CME) was successfully treated with aflibercept and pan-retinal photocoagulation (PRP). A 56-year-old male was sent to our uveitis service for further evaluation after a fluorescein angiogram revealed symmetric retinal ischemia for 360 degrees in both eyes. A fundus examination revealed an aneurysm, neuroretinitis, and occlusive vasculitis, all consistent with a diagnosis of IRVAN syndrome.
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