Abstract
We present a case of a woman with systemic lupus erythematosus (SLE) who had refractory episodes of neuromyelitis optica spectrum disorder (NMOSD) and was successfully treated with rituximab. She was positive for anti-aquaporin-4 (AQP4) antibody and had typical cranial and longitudinally extended spinal lesions but no optic nerve involvement. There is no established treatment for NMOSD/SLE overlap cases. Our experience suggests that rituximab may be effective for patients with combined SLE and anti-AQP4 antibody-positive NMOSD.
Original language | English |
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Pages (from-to) | 1374-1377 |
Number of pages | 4 |
Journal | Lupus |
Volume | 27 |
Issue number | 8 |
DOIs | |
Publication status | Published - Jul 1 2018 |
Keywords
- Anti-aquaporin-4 antibody
- neuromyelitis optica
- rituximab
- systemic lupus erythematosus
ASJC Scopus subject areas
- Rheumatology