Abstract

BackgroundNeuromyelitis optica (NMO) shows various brain magnetic resonance imaging (MRI) abnormalities with recurrent central nervous system (CNS) attacks, although predominantly affecting the spinal cord and optic nerve. However, NMO with extensive involvement of the brain has infrequently been studied. We investigated the clinical, radiographic features and immunomodulating changes of NMO patients with extensive brain lesions (EBLs) in China.MethodsNMO patients (including 16 NMO patients with EBLs and 53 NMO patients without EBLs) hospitalized during January 2006 and February 2010 were recruited and analyzed retrospectively. Data of clinical characteristics, magnetic resonance imaging (MRI) features, laboratory abnormalities, treatment details and outcomes were analyzed. All the patients received the follow-up visits for two years.ResultsEBLs in NMO were classified into four categories according to their respective MRI characteristics: 1) Tumefactive-like lesions (n=4, 25%); 2) Acute disseminated encephalomyelitis (ADEM)-like lesions (n=6, 37.5%); 3) Multiple sclerosis (MS)-like lesions (n=5, 31.25%); 4) Posterior reversible encephalopathy syndrome (PRES)-like lesions (n=1, 6.25%). NMO patients with EBLs had higher rates of encephalopathy symptoms (37.5% vs. 5.6%, p = 0.004), homonymous hemianopia (18.8% vs. 0%, p = 0.011) and AQP4 seropositivity (100% vs. 69.8%, p = 0.008) than NMO patients without EBLs (NEBLs). Immunomodulating changes (including the levels of C3, C4, ESR and CRP) were significantly higher in patients with EBLs than those without EBLs. The relapse times in EBLs during the follow-up period were more frequent than those happened in NEBLs (1.88 ± 0.30 vs. 1.23 ± 0.14, p = 0.04). The EDSS scores in EBLs patients were also much higher than those in NEBLs throughout all the whole visits of follow-up.ConclusionsThe presence of EBLs in NMO may indicate a higher diseases activity and portend a worse prognosis. CRP is a useful marker in monitoring diseases activity. Systemic inflammation may be crucial to the formation of EBLs in NMO.

Highlights

  • Neuromyelitis optica (NMO) shows various brain magnetic resonance imaging (MRI) abnormalities with recurrent central nervous system (CNS) attacks, predominantly affecting the spinal cord and optic nerve

  • Main characteristics of the study population All the subjects were classified into three groups: 1. extensive brain lesions (EBLs) (16 NMO patients with EBLs); 2

  • NEBLs* (37 AQP4-seropositive NMO patients without EBLs, all of whom are included in NEBLs)

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Summary

Introduction

Neuromyelitis optica (NMO) shows various brain magnetic resonance imaging (MRI) abnormalities with recurrent central nervous system (CNS) attacks, predominantly affecting the spinal cord and optic nerve. NMO with extensive involvement of the brain has infrequently been studied. Radiographic features and immunomodulating changes of NMO patients with extensive brain lesions (EBLs) in China. Neuromyelitis optica (NMO) is an autoimmune inflammatory and demyelinating disorder of the central nervous system (CNS), predominantly affecting the optic nerves and spinal cord. Several kinds of brain lesions detected by magnetic resonance imaging (MRI) have been considered as characteristics of NMO [4,6]. NMO with extensive involvement of the brain has only infrequently been studied on a large-sample basis, especially in the differences between the NMO patients with extensive brain lesions (EBLs) and those who without EBLs

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