Late-Onset Neuromyelitis Optica Spectrum Disorder: A Case Series From Iran Publisher Pubmed



Ghadiri F¹ ; Eskandarieh S¹ ; Sahraian MA¹ ; Azimi A¹ ; Moghadasi AN¹ Show Affiliations
Source: Revue Neurologique Published:2022

Abstract

Introduction: Neuromyelitis optica spectrum disorder (NMOSD) is a disabling autoimmune disease of the central nervous system that can start at ages of 50 or more, when it is called late-onset NMOSD (LO-NMOSD). Data on this disorder are sparse. In this cross-sectional study, patient characteristics of the disease were studied. LO-NMOSD patients of a tertiary center in Tehran were studied from 2016 to 2020. Case reports: Eight patients were identified, half of whom were men. The diagnostic delay was from no time-lapse to three years (mean: 0.62, SD: 1.06), which was significantly shorter than in early-onset patients. Seven patients (87.5%) tested positive for AQP4-IgG which was significantly higher compared to early-onset patients (p-value = 0.01). Four patients (50%) had both transverse myelitis and optic neuritis as presenting symptoms, while three (38%) had just myelitis and only one (12%) had optic neuritis. Conclusion: There is discrepancy regarding different aspects of LO-NMOSD. Further studies are needed to clarify the subject in order to enhance diagnosis and treatment. © 2021 Elsevier Masson SAS