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Lymphoplasmapheresis for Refractory Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report
Rui Tian1, Zhenglian Luo2, Zhen Hong1
1Department of Neurology and Institute of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Abstract:
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is generally responsive to immunotherapy, but some patients remain refractory despite treatment escalation. Lymphoplasmapheresis (LPE), a modified apheresis technique that removes both plasma components and circulating lymphocytes, may offer a salvage option in selected cases. We report a 61-year-old woman with refractory anti-NMDAR encephalitis who showed limited improvement after corticosteroids, intravenous immunoglobulin, and ofatumumab. After a prolonged interval following ofatumumab induction, she remained severely impaired with persistent disease activity and elevated cerebrospinal fluid and serum anti-NMDAR IgG titers. Three sessions of LPE were performed over 5 days. Clinical improvement was observed after LPE, accompanied by a decline in antibody titers. At 5-month follow-up after LPE, she maintained sustained recovery, with a Clinical Assessment Scale in Autoimmune Encephalitis score of 6 and a modified Rankin Scale score of 2. This case supports a close temporal association between LPE and clinical and immunological improvement, although causality cannot be definitively established from a single case.
Insights
Lymphoplasmapheresis (LPE) may be a valuable treatment for refractory anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. This case study shows LPE improved a patient
Area of Science:
- Neuroimmunology
- Neurology
- Immunotherapy
Background:
- Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune neurological disorder.
- While typically responsive to immunotherapy, some patients exhibit refractory disease.
- Salvage therapies are needed for treatment-resistant NMDAR encephalitis.
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