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Wyburn-Mason SyndromeReport of Two Cases Without Retinal Involvement
Dennis G. Brown, MD;
Sadek K. Hilal, MD;
Michael S. Tenner, MD
Arch Neurol. 1973;28(1):67-68.
Abstract
Two patients with unilateral optic atrophy had both suprasellar and intraorbital arteriovenous malformations. The first had associated vascular lesions of the ipsilateral mandible and maxilla, while the second had an ipsilateral facial vascular lesion. To our knowledge, these are the first reported cases of the Wyburn-Mason syndrome in which retinal arteriovenous malformations are absent despite extensive intraorbital involvement with the malformation.
Author Affiliations
New York
From the departments of neurology (Dr. Brown) and radiology (Drs. Hilal and Tenner), College of Physicians and Surgeons, Columbia University and the Neurological Institute of Columbia-Presbyterian Medical Center, New York. Dr. Tenner is now with the Department of Radiology, State University of New York, Downstate Medical Center, Brooklyn.
Footnotes
Accepted for publication Aug 18, 1972.
Read before the New York Neurological and Neurosurgical Society, New York, March 14, 1972.
Reprint requests to 710 W 168th St, New York 10032 (Dr. Brown).
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