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Hypertrophic pachymeningitis in polyarteritis nodosa: a case-based review
Shun Nomura1, Yasuhiro Shimojima2, Yasufumi Kondo1
1Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, 390-8621, Japan.
Hypertrophic pachymeningitis (HP), a rare dural thickening disorder, can be a rare neurological complication of polyarteritis nodosa (PAN). Prompt immunosuppressive treatment can lead to remission.
Area of Science:
- Neurology
- Immunology
- Rheumatology
Background:
- Hypertrophic pachymeningitis (HP) is a rare neurological disorder characterized by dural thickening.
- HP is often immune-mediated and associated with autoimmune diseases.
- Polyarteritis nodosa (PAN) is a systemic vasculitis with potential neurological manifestations.
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