Autoantibodies in Sporadic Creutzfeldt-Jakob Disease

被引:30
作者
Angus-Leppan, Heather [1 ,2 ]
Rudge, Peter [3 ,4 ]
Mead, Simon [3 ,4 ]
Collinge, John [3 ,4 ]
Vincent, Angela [5 ]
机构
[1] Royal Free London NHS Fdn Trust, London NW3 2QG, England
[2] Barnet Chase Farm Hosp NHS Trust, London, England
[3] Natl Hosp Neurol & Neurosurg, MRC Prion Unit, London WC1N 3BG, England
[4] Natl Hosp Neurol & Neurosurg, Natl Prion Clin, London WC1N 3BG, England
[5] John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England
关键词
D O I
10.1001/jamaneurol.2013.2077
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IMPORTANCE The diagnosis of autoimmune and neurodegenerative conditions can be unclear. Treatments such as removing the associated tumor, if present, and immunosuppression can halt or often reverse the progression of autoimmune conditions, but there is no curative treatment for neurodegenerative conditions. The presence of autoantibodies can sometimes be misleading. This report illustrates potential difficulties in differentiating autoimmune encephalopathies from sporadic Creutzfeldt-Jakob disease. OBSERVATIONS In a clinical follow-up of an older man with rapidly evolving encephalopathy at a neuroscience center, unsuccessful treatment with immunosuppression based on the incorrect presumptive diagnosis of Morvan syndrome was followed by the correct histological diagnosis of sporadic Creutzfeldt-Jakob disease. CONCLUSIONS AND RELEVANCE Autoimmune encephalopathies raise important treatment options and potential for recovery. However, since neuronal antibodiesmay be positive in prion disease, interpretation can be complex and must be rooted in the clinical picture.
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页码:919 / 922
页数:4
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