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From: TSS ()
Subject: sporadic CJD: Clinical and diagnostic characteristics of the rare VV1 type
Date: October 17, 2005 at 7:59 am PST

Published online before print October 12, 2005
(Neurology 2005, doi:10.1212/01.wnl.0000184674.32924.c9)

Received February 24, 2005
Accepted August 24, 2005

Sporadic Creutzfeldt-Jakob disease: Clinical and diagnostic characteristics of the rare VV1 type
B. Meissner MD, I. M. Westner MD, K. Kallenberg MD, A. Krasnianski MD, M. Bartl MD, D. Varges , C. Bösenberg , H. A. Kretzschmar MD, FRCPath, M. Knauth MD, W. J. Schulz-Schaeffer MD, and I. Zerr MD*

From the Departments of Neurology (Drs. Meissner, Krasnianski, Bartl, Zerr, D. Varges and C. Bösenberg), Neuroradiology (Drs. Kallenberg and Knauth), and Neuropathology (Dr. Schulz-Schaeffer), Georg-August-Universität Göttingen; and Center for Neuropathology and Prion Research (Drs. Westner and Kretzschmar), Ludwig-Maximilians-Universität München, Germany.


* To whom correspondence should be addressed. E-mail: IngaZerr@med.uni-goettingen.de .


Abstract-- Background: Recently, six molecular subtypes of sporadic CJD (sCJD) have been identified showing differences regarding the disease course, neuropathologic lesion patterns, and sensitivity to diagnostic tools. Only isolated cases of the rare VV1 type have been reported so far. Objective: To describe the clinical characteristics and neuropathologic lesion profiles in nine cases. Methods: In the years 1993 until late 2003, 571 definite neuropathologically confirmed cases of sporadic CJD were identified in Germany. Of these, nine were homozygous for valine and displayed type 1 of the pathologic PrPSc in the brain (VV1 type). Results: The authors describe eight men and one woman belonging to the VV1 type. All patients were relatively young at disease onset (median 44 years vs 65 years in all sCJD) with prolonged disease duration (median 21 months vs 6 months in all sCJD). During the initial stages, their main clinical signs were personality changes and slowly progressive dementia as well as focal neurologic deficits. None of the nine VV1 patients had periodic sharp-wave complexes (PSWCs) in the EEG. Only two out of seven displayed the typical signal increase of the basal ganglia on MRI, whereas signal increase of the cortex was seen in all patients. The 14-3-3 protein levels were elevated in CSF in all cases tested. Conclusions: The clinical diagnosis of the VV1 type of sCJD can be best supported by the 14-3-3 test and cortical signal increase on MRI. Because of the young age at onset vCJD is sometimes suspected as a differential diagnosis. MRI plays an important role in differentiating these two disease types and should be performed early during the disease course.

http://www.neurology.org/cgi/content/abstract/01.wnl.0000184674.32924.c9v1

TSS




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