Wyburn-Mason Syndrome: A Case Report.

Shin, Chang Hyun; Lee, Su Na

doi:2010.51.1.145

J Korean Ophthalmol Soc > Volume 51(1); 2010 > Article

Case Report

Journal of the Korean Ophthalmological Society 2010;51(1):145-149.
DOI: https://doi.org/10.3341/jkos.2010.51.1.145 Published online January 15, 2010.

Wyburn-Mason Syndrome: A Case Report.

Chang Hyun Shin, Su Na Lee

Department of Ophthalmology, Eulji University Hospital, College of Medicine, Daejeon, Korea. snlee@eul.ji.ac.kr

뇌실내 출혈을 동반한 와이번 메이슨 증후군 1예

신창현ㆍ이수나

Department of Ophthalmology, Eulji University Hospital, College of Medicine, Daejeon, Korea

Abstract

PURPOSE
To describe a case of Wyburn-Mason Syndrome, which is characterized by arteriovenous malformations in the central nervous system and the retina. CASE SUMMARY: A 13-year-old girl who underwent neurosurgical intervention for intraventricular hemorrhage was referred to our ophthalmic clinic because brain angiogram and MRI finding revealed arteriovenous malformations (AVMs) that extended from the orbit and optic chiasm along the optic pathway. Fundus and fluorescein angiography of the left eye showed marked dilation and tortuosity of the retinal vessels. Fluorescein angiographic findings showed rapid filling of all vessels and no dye leakage. CONCLUSIONS: Retinal racemose hemangioma should be considered for Wyburn-Mason syndrome, and the finding of retinal AVMs should warrant cerebral imaging studies including MRI and angiography.

Key Words: Wyburn Mason syndrome;Arteriovenous malformation;Retinal racemose hemangioma