Radiologically isolated aquaporin-4 antibody neuromyelitis optica spectrum disorder.
Omar A Abdel-MannanAinat KleinAnat Bachar ZiporiLiat Ben-SiraAviva Fattal-ValevskiYael HacohenHadas MeirsonPublished in: Multiple sclerosis (Houndmills, Basingstoke, England) (2022)
Aquaporin-4 antibody (AQP4-Ab) Neuromyelitis Optica Spectrum Disorder (NMOSD) is a rare neuroinflammatory syndrome presenting predominantly with optic neuritis and transverse myelitis. We report a case of radiologically isolated longitudinally extensive optic neuritis in an asymptomatic 12-year-old female with positive serum AQP4-Ab, with resolution of imaging changes after immune therapy. By contrast to patients with radiologically isolated syndrome, of which some will never convert to multiple sclerosis, the pathogenicity of AQP4-Ab in the context of sub-clinical disease, supported treatment in our patient. Given the severe morbidity in AQP4-Ab NMOSD, prognostic biomarkers for disease severity are required to guide optimal therapy for patients.
Keyphrases
- spectrum disorder
- case report
- multiple sclerosis
- end stage renal disease
- newly diagnosed
- optical coherence tomography
- ejection fraction
- chronic kidney disease
- high resolution
- magnetic resonance
- peritoneal dialysis
- early onset
- stem cells
- escherichia coli
- staphylococcus aureus
- mass spectrometry
- white matter
- mesenchymal stem cells
- optic nerve
- pseudomonas aeruginosa