Signs of rapidly progressive dementia in a case of intravascular lymphomatosis
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 m...
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Veröffentlicht in: | European archives of psychiatry and clinical neuroscience 2005-08, Vol.255 (4), p.232-235 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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). |
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ISSN: | 0940-1334 1433-8491 |
DOI: | 10.1007/s00406-004-0551-9 |