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Devic’s syndrome in aquaporin-4 antibody negative patient. What we need to know …

机译:Aquaporin-4抗体阴性患者的Devic综合征。我们需要知道的...

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摘要

>Introduction: Neuromyelitis optica (NMO) is a severe demyelinating syndrome characterized by optic neuritis (ON) and acute myelitis. The NMO spectrum is actually recognized to typically evolve as a relapsing disorder that also includes patients with atypical unilateral ON and those with index events of ON and myelitis occurring weeks or even years apart (Jarius/Wildemann 2013). NMO was previously assumed to be a variant of multiple sclerosis (MS), but the discovery of aquaporin-4 antibodies in patients with neuromyelitis optica has led to this view being revised (Mandler 2006, Barnett/Sutton 2012, Wingerchuk et al. 2007). The cause of the condition is still unknown, but it has been shown that the antibodies bind selectively to a water channel expressed mainly on astrocytes at the blood-brain-barrier, which has an important role in the regulation of brain volume and ion homeostasis. However, there are some patients with NMO that are antibodies negative. The diagnosis is made on the basis of case history, clinical examination, magnetic resonance imaging (MRI) of the brain and spinal cord, analysis of cerebrospinal fluid (CSF), visual evoked potentials and a blood test with analysis of aquaporin-4 antibodies (Barnett/Sutton 2012, Wingerchuk et al. 2007, Thornton et al. 2011). This suggests that periodical revisions of established concepts and diagnostic criteria are necessary.>Purpose: The authors describe an extremely rare case of neuromyelitis optica and the aim of this paper is to call attention for the cases of NMO whith NMO-IgG negative.>Methods: The selected method is a case report.>Results: To date the patient showed partial recovery of left eye acuity and improvement of muscle strength of upper and lower limbs and does not show recurrence of the disease.>Conclusion: NMO has a distinct clinical, imaging and immunopathological features sufficient to distinguish it from MS. This distinction is essential, because the treatment and the prognosis is different.
机译:>简介:视神经脊髓炎(NMO)是一种以视神经炎(ON)和急性脊髓炎为特征的严重脱髓鞘综合征。实际上,人们公认NMO谱通常会发展为复发性疾病,其中还包括非典型性单侧ON的患者以及具有指数事件的ON和脊髓炎发生于几周甚至数年的患者(Jarius / Wildemann 2013)。 NMO以前被认为是多发性硬化症(MS)的变体,但是在视神经脊髓炎患者中发现aquaporin-4抗体导致这一观点被修订(Mandler 2006,Barnett / Sutton 2012,Wingerchuk等人2007)。 。病情的原因仍然未知,但已显示抗体选择性结合主要在血脑屏障上星形胶质细胞上表达的水通道,这在调节脑容量和离子稳态中具有重要作用。但是,有些NMO患者的抗体阴性。诊断的依据是病史,临床检查,脑和脊髓的磁共振成像(MRI),脑脊液(CSF)分析,视觉诱发电位以及对水通道蛋白4抗体进行分析的血液检查( Barnett / Sutton,2012年,Wingerchuk等,2007年,Thornton等,2011年)。这表明必须对既定的概念和诊断标准进行定期修订。>目的:作者描述了一种极为罕见的视神经脊髓炎病例,本文旨在提请注意NMO的NMO病例。 -IgG阴性。>方法:所选方法为一例病例报告。>结果:迄今为止,患者显示左眼视力部分恢复并且上下肌肉力量得到改善>结论:NMO具有明显的临床,影像学和免疫病理学特征,足以将其与MS区别开来。这种区别至关重要,因为治疗和预后不同。

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