IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report

Abstract

Abstract Nervous system involvement in IgG4‐related systemic disease (IgG4‐RD) is rarely reported and manifests as hypertrophic pachymeningitis and hypophysitis. In this report, a 33‐year‐old woman with neurological manifestations was diagnosed with IgG4‐RD by biopsy. The patient showed improvement in symptoms after treatment.

Keywords

• cerebral venous thrombosis
• IgG4‐related disease
• pachymeningitis