1. Pathological findings of hypertrophic pachymeningitis associated with eosinophilic granulomatosis with polyangiitis.
- Author
-
Shiraishi W, Tsujimoto Y, and Shiraishi T
- Subjects
- Humans, Churg-Strauss Syndrome complications, Churg-Strauss Syndrome diagnosis, Eosinophilia, Granulomatosis with Polyangiitis complications, Granulomatosis with Polyangiitis diagnosis, Meningitis etiology
- Abstract
The most common neurological manifestation of eosinophilic granulomatosis with polyangiitis (EGPA), formerly called Churg-Strauss syndrome, is mononeuritis multiplex caused by small-vessel vasculitis. In contrast, central nervous system involvement is rare. Among EGPA-associated central nervous system disorders, there are only a few reported cases of hypertrophic pachymeningitis (HP). Here, we report a patient with EGPA with headache and ophthalmoplegia who presented with HP and had a dural biopsy. The biopsy specimen showed lymphocytic inflammatory cell infiltration without EGPA-specific findings, that is, eosinophilic infiltration, granuloma or angiitis. To the best of our knowledge, there are no previous reports of EGPA-associated HP pathology. Here, we report the first case presentation of a patient with EGPA-associated HP with pathological findings., Competing Interests: Competing interests: None declared., (© BMJ Publishing Group Limited 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
- Published
- 2021
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