IgG4 Related Disease associated with the primary manifestation of
recurrent Cerebral Venous Thrombosis: a rare case report
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 the treatment.