Signs of rapidly progressive dementia in a case of intravascular lymphomatosis

被引:7
|
作者
Albrecht, R
Krebs, B
Reusche, E
Nagel, M
Lencer, R
Kretzschmar, H
机构
[1] Ludwig Maximilians Univ Munchen, Inst Neuropathol, D-81377 Munich, Germany
[2] Univ Lubeck, Inst Pathol, Lubeck, Germany
[3] Univ Lubeck, Dept Psychiat, Lubeck, Germany
关键词
dementia; intravascular lymphomatosis; non-Hodgkin's lymphoma; primary angiitis of the CNS; Creutzfeldt-Jakob disease;
D O I
10.1007/s00406-004-0551-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Intravascular lymphomatosis (IVL), a rare type of non-Hodgkin's lymphoma, is an uncommon cause of progressive dementia, usually followed by death within a few months of onset of clinical disease. Often this aggressive tumor is only diagnosed at autopsy, because of misleading clinical features mimicking a broad spectrum of syndromes and the absence of circulating lympoma cells in the blood, bone marrow or cerebrospinal fluid in many cases. Here we present IVL in a 78-year-old woman with findings leading to the clinical diagnosis of vascular dementia with sudden beginning and positive 14-3-3 protein in the CSF, commonly reported in Creutzfeldt-Jakob disease (CJD).
引用
收藏
页码:232 / 235
页数:4
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