Abstract
Introduction:Glial fibrillary acidic protein (GFAP) immunoglobulin G is a recently discovered biomarker of an autoimmune central nervous system disorder characterized by a steroid-responsive meningoencephalomyelitis.Case Report:A 63-year-old man with rheumatoid arthritis on etanercept presented with steroid-responsive subacute encephalopathy and foot drop. Brain and sural nerve biopsies demonstrated a T-cell perivascular infiltrate. Cerebrospinal fluid studies 18 months into the course of the illness demonstrated a GFAP antibody on mouse tissue immunofluorescence confirmed by cell-based assay. The patient was treated with steroids and cyclophosphamide leading to resolution of his symptoms.Conclusion:This case expands on the previously reported cases of GFAP immunoglobulin G autoimmunity by describing an associated inflammatory large fiber peripheral neuropathy.
Original language | English (US) |
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Pages (from-to) | 152-154 |
Number of pages | 3 |
Journal | Neurologist |
Volume | 24 |
Issue number | 5 |
DOIs | |
State | Published - Sep 1 2019 |
Keywords
- GFAP
- TNF-inhibitor
- encephalopathy
- neuroimmunology
- neuropathy
ASJC Scopus subject areas
- Clinical Neurology