Authors
Miyuki Miyamoto, Yuma Sato, Nobuyuki Ishii
Published in
Internal medicine (Tokyo, Japan). Oct 15, 2026. Epub Oct 15, 2026.
Abstract
Neuromyelitis optica spectrum disorder (NMOSD) rarely presents with corticalleptomeningeal involvement. A 47-year-old woman with aquaporin-4 immunoglobulin G (AQP4-IgG)-positive NMOSD developed acute headache, seizures, motor aphasia, and worsening right arm weakness. Brain magnetic resonance imaging revealed a tumefactive-appearing left frontal cortical-subcortical lesion with leptomeningeal enhancement. The clinical and radiological abnormalities improved after immunotherapy. This case illustrates a rare cerebral manifestation of AQP4-IgG-positive NMOSD with cortical-leptomeningeal involvement, seizures, and a tumefactive lesion.
PMID:
42875206
Bibliographic data and abstract were imported from PubMed on 15 Oct 2026.
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