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BRIEF COMMUNICATION
Year : 2011  |  Volume : 59  |  Issue : 3  |  Page : 240-241

Frosted branch angiitis, neuroretinitis as initial ocular manifestation in Behçet disease


Department of Ophthalmology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman

Correspondence Address:
Upender K Wali
Department of Ophthalmology, Sultan Qaboos University Hospital, 123 Al-Khod, Muscat
Oman
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.81048

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Behçet disease is an idiopathic, multisystem disorder characterized by recurrent episodes of orogenital ulceration and vasculitis of the veins and arteries of all calibers. Ocular involvement may affect the conjunctiva, sclera, uveal tract, vitreous, blood vessels, and retina. Many theories have pointed toward an autoimmune response behind its pathogenesis, which may be triggered by exposure to an infectious agent. Frosted branch angiitis is characterized by vascular inflammation, sheathing, retinal edema, and retinal hemorrhages. The disease may be idiopathic in a majority of the cases or may be associated with ocular and systemic pathology. Association between Behηet disease, Frosted branch angiitis, and neuroretinitis is not reported in literature. This uncommon combination reflects the varied systemic and ocular manifestations in Behηet disease, especially in patients who are not diagnosed and treated in time. We hereby report a case of bilateral frosted branch angiitis and neuroretinitis in a young male from Middle-east, suffering from Behçet disease.


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