DR. SONY CHAUDHARY

DR. BRIJESH KUMAR KUSHWAHA, DR. KIRTI VERMA, DR. SANJAY BOSAK

Abstract

AIM: Sturge–Weber angiomatosis is a rare, nonhereditary developmental condition characterized by a hamartomatous vascular proliferation involving the tissues of brain and face. A report a similar case in 24yr male. METHODS: A 24yr male presented with diminution of vision in both eye for last 8yr. RESULTS: Vision was 6/24 in right eye and 6/9 in his left eye. On systemic examination port wine stain was seen on right side of face involving the eye, half of nose, cheek, philtrum, and left side of upper lip. On ocular examination there was glaucomatous optic atrophy with CD ratio 0.99 in right eye and 0.6 in left eye. He underwent trabeculectomy in both eyes. CONCLUSIONS: Early diagnosis and appropriate treatment plan is imperative to prevent development of complications.