| Literature DB >> 24171831 |
Halil Ibrahim Onder1, Sibel Alisan, Murat Tunc.
Abstract
Wyburn-Mason syndrome is a rare phacomatosis characterized by unilateral arteriovenous malformations (AVMs) involving the brain, retina, and (rarely) the skin. The diagnosis is concluded with dilated fundus examination and markedly dilated tortuous vascular loops with arteriovenous communications on fluorescent angiography. We present a 14-year-old male patient with Wyburn-Mason syndrome who developed serous macular neuroretinal detachment, cystoid macular edema (CME), and consequent visual deterioration in the left eye. To the best of our knowledge, this is the first report of a patient with Wyburn-Mason syndrome who developed serous retinal detachment and CME.Entities:
Keywords: Arteriovenous malformations; cystoid macular edema; serous macular neuroretinal detachment; triamcinolone; wyburn-Mason syndrome
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Year: 2013 PMID: 24171831 DOI: 10.3109/08820538.2013.835832
Source DB: PubMed Journal: Semin Ophthalmol ISSN: 0882-0538 Impact factor: 1.975