Paraneoplastic neurological syndromes and autoimmune encephalitis

被引:0
|
作者
Stich, O. [1 ]
Rauer, S. [1 ]
机构
[1] Univ Klin Freiburg, Neurozentrum, Abt Neurol & Neurophysiol, D-79106 Freiburg, Germany
来源
NERVENARZT | 2014年 / 85卷 / 04期
关键词
Antineuronal antibodies; Autoimmune encephalitis; Limbic encephalitis; Paraneoplastic cerebellar degeneration; Subacute sensory neuropathy; CELL LUNG-CANCER; NMDA RECEPTOR ENCEPHALITIS; EATON MYASTHENIC SYNDROME; LIMBIC ENCEPHALITIS; CEREBELLAR DEGENERATION; SENSORY NEURONOPATHY; DIAGNOSTIC-CRITERIA; ANTI-YO; ANTIBODIES; AUTOANTIBODIES;
D O I
10.1007/s00115-014-4030-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Paraneoplastic neurological syndromes (PNS) are defined as remote effects on the central and peripheral nervous system that are not caused directly by the tumor, its metastases and treatment, or metabolic disorders. The most probable cause is a falsely initiated immune reaction. Well-defined classical PNSs are associated with distinct tumors and occur with onconeural antibodies directed against intracellular neuronal antigens. However, response to therapy is limited. Recently, new antibodies directed against neuronal surface antigens were described in encephalitic syndromes of autoimmune origin. These probably antibody-mediated disorders are more frequent than classical PNS, occur with or without tumor association and often show a good response to immunosuppressive treatment.
引用
收藏
页码:485 / 498
页数:14
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