Anomalous optical coherence tomography findings in Wyburn-Mason syndrome and isolated retinal arteriovenous malformation

Margaret J. Chowaniec, Donny W. Suh, H. Culver Boldt, Steven F. Stasheff, Paul M. Beer, Gerard P. Barry

Research output: Contribution to journalArticle

4 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)175-177
Number of pages3
JournalJournal of AAPOS
Volume19
Issue number2
DOIs
StatePublished - Apr 1 2015

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Ophthalmology

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