Abstract |
Wyburn-Mason syndrome (WMS) is a rare congenital disease that presents with unilateral arteriovenous malformation (AVM) in the visual pathway, midbrain, and/or skin. We report a case of a 5-year-old girl with a history of cerebral and orbital AVM who presented with left exotropia and was found to have group 3 retinal AVM consistent with WMS. Here, we use ultrawide field imaging to show the progression of retinal AVM and peripheral nonperfusion areas for a period of 1 year in a pediatric patient with WMS. [Ophthalmic Surg Lasers Imaging Retina. 2022;53:46-48.].
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Authors | Charlene H Choo, Irena Tsui, Ronald J Homer, Soh Youn Suh |
Journal | Ophthalmic surgery, lasers & imaging retina
(Ophthalmic Surg Lasers Imaging Retina)
Vol. 53
Issue 1
Pg. 46-48
(01 2022)
ISSN: 2325-8179 [Electronic] United States |
PMID | 34982002
(Publication Type: Case Reports, Journal Article)
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Topics |
- Arteriovenous Fistula
(complications, diagnosis)
- Arteriovenous Malformations
(diagnosis)
- Child
- Child, Preschool
- Female
- Hemangioma
- Humans
- Neurocutaneous Syndromes
(diagnosis)
- Retinal Artery
(abnormalities, diagnostic imaging)
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