Abstract
Introduction: Behçet’s syndrome is a multisystemic, chronic inflammatory disease characterized by recurrent oral and genital ulcers, ocular inflammation, arthritis, and skin lesions. Neurological impairment makes the severity of Behçet’s disease, it most
Highlights
Behçet’s syndrome is a multisystemic, chronic inflammatory disease characterized by recurrent oral and genital ulcers, ocular inflammation, arthritis, and skin lesions
Neuro-Behçet’s disease is rare, including the pseudo-tumoral form, and can exceptionally be its initial mode of presentation. It can be established in two different patterns: parenchymal and non-parenchymal
We describe a case of neuro-Behçet’s syndrome presenting with features mimicking brain tumors
Summary
Neuro-Behçet’s disease is rare, including the pseudo-tumoral form, and can exceptionally be its initial mode of presentation.
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