Abstract
IgG4-related disease (IgG4RD) with intracranial involvement is rare. We report a 56-year-old male who had an excellent response to rituximab and dexamethasone after going undiagnosed for 5 years. After 3 years of rituximab maintenance, he has no evidence of disease on brain MRI.
Original language | English (US) |
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Pages (from-to) | 1610-1614 |
Number of pages | 5 |
Journal | Clinical Case Reports |
Volume | 9 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2021 |
Keywords
- IgG4 disease
- headache
- lymphoproliferative disorder
- maintenance rituximab
- pachymeningitis
ASJC Scopus subject areas
- Medicine(all)