Wegener's Granulomatosis (WG) is an uncommon systemic vasculitic disease involving the respiratory system and kidneys. It is the most common antineutrophil cytoplasm antibody (ANCA)-associated vasculitis. Orbital involvement in WG is a rare but potentially devastating disorder leading to visual loss and deformity. Most clinical characteristics of this disease are non-specific, making clinical diagnosis nearly impossible. We reviewed the features of WG involving the orbit including radiologic, serologic, and histopathologic findings. Advances in treatment are likewise discussed.
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Santiago et al. (2011) studied this question.
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