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Emergence of A New Entity: The Autoimmune Encephalitis

机译:新实体的出现:自身免疫性脑炎

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Encephalitis has been known as a distinct entity for a long time but it’s exact cause has remained undetected in about half the cases in spite of extensive investigations. During the last few years there has been reports of cases of encephalitis in which antibodies has been detected against deep grey matter neurons. Antibodies have been detected against the N-methyl-D-aspartate (NMDA) receptors or voltage-gated potassium channels (VGKC). VGKC antibody positive encephalitis usually presents in middle aged or elderly people and is twice as common in men. The main symptoms are memory loss and seizures. Cognitive impairment, confusion, disorientation, personality change and behavioral disturbances are also common. Encephalitis associated with NMDA receptor antibodies is mainly seen in children and young adults, with women being affected about three to four times more often than men. Initially there is a period of cognitive impairment and psychiatric features like hallucinations, agitation and depression but later there is gradual deterioration in conscious level with autonomic features often requiring intensive care. The most striking feature of both these types of encephalitis is their uniform good response to immunomodulating therapies. Intravenous immunoglobulin (IVIG), glucocorticosteroids, plasma exchange and drugs like cyclophosphamide, rituximab, mycophenolate mofetil, azathioprine, singly or in combination have all produced good results. It is this surprisingly easily available effective treatment which makes diagnosis of this condition imperative. Encephalitis is a condition which is encountered by physicians at all levels and so a high level of awareness about the condition will ensure that the condition is not missed. This review about this new condition is being presented to make physicians aware about this devastating but easily treatable disease. DOI: http://dx.doi.org/10.3329/jom.v13i2.12755 J Medicine 2012; 13 : 179-189
机译:脑炎被称为截然不同的实体,但尽管大约一半的病例,但它的确切原因在案件中仍然未被发现,尽管有广泛的调查。在过去的几年中,已经报道了脑炎病例,其中针对深灰质神经元检测到抗体。已针对N-甲基-D-天冬氨酸(NMDA)受体或电压门控钾通道(VGKC)检测抗体。 VGKC抗体阳性脑炎通常在中年或老年人中呈现,并且是男性的两倍。主要症状是内存损耗和癫痫发作。认知障碍,混乱,迷失化,性格变化和行为紊乱也很常见。与NMDA受体抗体相关的脑炎主要是在儿童和年轻人中看到的,女性受到比男性更频繁的三到四倍。最初存在一段时间的认知障碍和精神病特征,如幻觉,激动和抑郁,但后来有意识级别的自主特征逐渐恶化,通常需要重症监护。这两种类型的脑炎的最引人注目的特征是它们对免疫调节疗法的均匀反应。静脉内免疫球蛋白(IVIG),糖皮质激素,血浆交换和药物,如环磷酰胺,Rituximab,霉酚酸酯,偶氮唑,单独或组合都具有所有产生的良好结果。这是令人惊讶的易于可用的有效处理,这使得这种条件的诊断势在必行。脑炎是一种条件,受到各级的医生遇到的,因此对这种情况的高度认识将确保不会错过这种情况。正在提出这篇关于这种新条件的审查,使医生意识到这种破坏性但容易治疗的疾病。 DOI:http://dx.doi.org/10.3329/jom.v13i2.12755 J医学2012; 13:179-189

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