1. Anomalous optical coherence tomography findings in Wyburn-Mason syndrome and isolated retinal arteriovenous malformation.
- Author
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Chowaniec MJ, Suh DW, Boldt HC, Stasheff SF, Beer PM, and Barry GP
- Subjects
- Arteriovenous Fistula physiopathology, Arteriovenous Malformations physiopathology, Child, Child, Preschool, Female, Humans, Magnetic Resonance Angiography, Male, Neurocutaneous Syndromes physiopathology, Visual Acuity physiology, Visual Fields physiology, Arteriovenous Fistula diagnosis, Arteriovenous Malformations diagnosis, Neurocutaneous Syndromes diagnosis, Retinal Artery abnormalities, Retinal Vein abnormalities, Tomography, Optical Coherence
- Abstract
We report 2 cases of unilateral retinal arteriovenous malformation (AVM) with previously unreported anomalies of the inner retinal layers detected on spectral domain optical coherence tomography (SD-OCT): a 5-year-old girl with a large unilateral retinal AVM, ipsilateral visual acuity of 20/200, and ipsilateral intracranial AVM; and a 10-year-old boy with a large unilateral retinal AVM, ipsilateral visual acuity of 20/20, ipsilateral temporal visual field defects, and no intracranial AVM. Both macular SD-OCT findings showed multiple large inner retinal vessels that created a prominent shadowing artifact, retinal thickening, and speckling and heterogeneity of inner retinal layers., (Copyright © 2015 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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