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Signs of rapidly progressive dementia in a case of intravascular lymphomatosis.

Authors :
Albrecht, R.
Krebs, B.
Reusche, E.
Nagel, M.
Lencer, R.
Kretzschmar, H. A.
Source :
European Archives of Psychiatry & Clinical Neuroscience; 2005, Vol. 255 Issue 4, p232-235, 4p, 2 Color Photographs
Publication Year :
2005

Abstract

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). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09401334
Volume :
255
Issue :
4
Database :
Complementary Index
Journal :
European Archives of Psychiatry & Clinical Neuroscience
Publication Type :
Academic Journal
Accession number :
17941185
Full Text :
https://doi.org/10.1007/s00406-004-0551-9