Abstract
Background: The adult orbital xanthogranulomatous disease (AOXGD) is a rare and poorly understood heterogeneous group of syndromes with variable clinical features. They share similar histopathological characters including infiltration of foamy histiocytes, Touton-type giant cells and accompanying lymphocytes into the soft tissue. The golden diagnostic standard for AOXGD is to combine both histopathological features and clinical presentation.
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