Tc-99m-bicisate (ECD)-brain-SPECT in rapidly progressive dementia

被引:0
作者
Marienhagen, J [1 ]
Weingärtner, U
Zerr, I
Poser, S
Blaha, L
Eilles, C
机构
[1] Univ Regensburg Klinikum, Abt Nukl Med, D-93042 Regensburg, Germany
[2] Bezirkskrankenhauses Mainkofen, Psychiat Klin, Gottingen, Germany
[3] Univ Gottingen, Neurol Klin & Poliklin, Prionenforschungsgrp, D-3400 Gottingen, Germany
关键词
dementia; brain-SPECT; Creutzfeldt-Jakob-disease; Tc-99m-bicisafe; neuron-specific enolase; 14-3-3; Protein;
D O I
暂无
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We present a 61-year-old male patient with progressive dementia. A brain SPECT with Tc-99m-bicisate was performed for confirmation of clinically suspected Alzheimer-dementia. At the lime of the SPECT-investigation marked apraxia and aphasia besides severe dementia were present. Electrophysiological as well as anatomical neuroimaging findings showed non-diagnostic alterations. SPECT revealed distinct perfusion defects, which made Alzheimer Dementia unlikely. The further course of the patient was determined by rapidly progressive deterioration with development of akinetic mutism. Thereafter increased levels of neuron-specific enolase as well as 14-3-3 proteins were found in the cerebro-spinal fluid (CSF). The patient finally died with signs of cerebral decortication. Due to the clinical course and the CSF-findings the patient's final diagnosis was Creutzfeldt-Jakob-disease, nevertheless no autopsy was performed. The presented case report underscores the clinical utility of perfusion brain SPECT in the differential diagnosis of dementias.
引用
收藏
页码:203 / 206
页数:4
相关论文
共 10 条
[1]   MR imaging of Creutzfeldt-Jakob disease [J].
Finkenstaedt, M ;
Szudra, A ;
Zerr, I ;
Poser, S ;
Hise, JH ;
Stoebner, JM ;
Weber, T .
RADIOLOGY, 1996, 199 (03) :793-798
[2]  
Grunwald F, 1996, Ann Nucl Med, V10, P131
[3]   The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies [J].
Hsich, G ;
Kinney, K ;
Gibbs, CJ ;
Lee, KH ;
Harrington, MG .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (13) :924-930
[4]   CREUTZFELDT-JAKOB DISEASE - PATTERNS OF WORLDWIDE OCCURRENCE AND THE SIGNIFICANCE OF FAMILIAL AND SPORADIC CLUSTERING [J].
MASTERS, CL ;
HARRIS, JO ;
GAJDUSEK, DC ;
GIBBS, CJ ;
BERNOULLI, C ;
ASHER, DM .
ANNALS OF NEUROLOGY, 1979, 5 (02) :177-188
[5]   Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease [J].
Parchi, P ;
Castellani, R ;
Capellari, S ;
Ghetti, B ;
Young, K ;
Chen, SG ;
Farlow, M ;
Dickson, DW ;
Sima, AAF ;
Trojanowski, JQ ;
Petersen, RB ;
Gambetti, P .
ANNALS OF NEUROLOGY, 1996, 39 (06) :767-778
[6]   Creutzfeldt-Jakob disease, a sphinx of current neurobiology [J].
Poser, S ;
Zerr, I ;
SchulzSchaeffer, WJ ;
Kretzschmar, HA ;
Felgenhauer, K .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1997, 122 (37) :1099-1105
[7]   THE VALUE OF SPET IMAGING IN DEMENTIA [J].
TALBOT, PR ;
TESTA, HJ .
NUCLEAR MEDICINE COMMUNICATIONS, 1995, 16 (06) :425-437
[8]   Expanded disease spectrum of human spongiform encephalopathies or prion diseases [J].
Weber, T ;
Zerr, I ;
Bodemer, M ;
Poser, S .
NERVENARZT, 1997, 68 (04) :309-323
[9]   Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease [J].
Zerr, I ;
Bodemer, M ;
Gefeller, O ;
Otto, M ;
Poser, S ;
Wiltfang, J ;
Windl, O ;
Kretzschmar, HA ;
Weber, T .
ANNALS OF NEUROLOGY, 1998, 43 (01) :32-40
[10]   CEREBROSPINAL-FLUID CONCENTRATION OF NEURON-SPECIFIC ENOLASE IN DIAGNOSIS OF CREUTZFELDT-JAKOB-DISEASE [J].
ZERR, I ;
BODEMER, M ;
RACKER, S ;
GROSCHE, S ;
POSER, S ;
KRETZSCHMAR, HA ;
WEBER, T .
LANCET, 1995, 345 (8965) :1609-1610