New variant Crutzfeldt-Jakob disease: psychiatric features

被引:123
作者
Zeidler, M [1 ]
Johnstone, EC [1 ]
Bamber, RWK [1 ]
Dickens, CM [1 ]
Fisher, CJ [1 ]
Francis, AF [1 ]
Goldbeck, R [1 ]
Higgo, R [1 ]
JohnsonSabine, EC [1 ]
Lodge, GJ [1 ]
McGarry, P [1 ]
Mitchell, S [1 ]
Tarlo, L [1 ]
Turner, M [1 ]
Ryley, P [1 ]
Will, RG [1 ]
机构
[1] WESTERN GEN HOSP,NATL CREUTZFELDT JAKOB DIS SURVEILLANCE UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
关键词
D O I
10.1016/S0140-6736(97)03148-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background An apparently new variant of Creutzfeldt-Jakob disease (CJD), new variant CJD [nvCJD), was identified in the UK in 1996. There have now been 21 cases of nvCJD in the UK and one in France, Psychiatric symptoms are prominent in the initial presentation in these cases. Methods Cases of nvCJD are identified mainly by direct referral horn neurologists and neuropathologists. Detailed clinical information was obtained by review of case notes and interviewing patients' relatives. We report the psychiatric features of the first 14 cases on nvCJD in the UK. Psychiatric notes were examined in ail 13 of these cases who were seen by a psychiatrist. Results Eight cases were women. Ali 14 cases had early psychiatric features and in nine, the first symptom was psychiatric. 13 cases were seen by a psychiatrist and the majority were diagnosed as suffering from depression or depression secondary to organic disease. Two cases suffered from first-rank symptoms suggestive of psychotic illness and transient delusions and auditory or visual hallucinations occurred in the majority. Aii cases were referred to a neurologist as the illness evolved and neurological signs developed. Interpretation Psychiatric symptoms are a consistent early clinical feature in nvCJD. Analysis of the psychiatric symptoms does not suggest specific features that readily allow distinction from more common psychiatric disorders, although the occurrence of associated persistent sensory symptoms may raise the possibility of this diagnosis. Neurological signs, including ataxia, involuntary movements and cognitive impairment developed in ail cases and the evolution of increasing neurological deficits is likely to remain critical to the clinical diagnosis of nvCJD.
引用
收藏
页码:908 / 910
页数:3
相关论文
共 17 条
[1]   CREUTZFELDT-JAKOB DISEASE MISDIAGNOSED AS DEPRESSIVE PSEUDODEMENTIA [J].
AZORIN, JM ;
DONNET, A ;
DASSA, D ;
GAMBARELLI, D .
COMPREHENSIVE PSYCHIATRY, 1993, 34 (01) :42-44
[2]   VISUAL HALLUCINATIONS AND SENSORY DELUSIONS IN THE ELDERLY [J].
BERRIOS, GE ;
BROOK, P .
BRITISH JOURNAL OF PSYCHIATRY, 1984, 144 (JUN) :662-664
[3]   CREUTZFELDT-JAKOB DISEASE IN FRANCE .2. CLINICAL CHARACTERISTICS OF 124 CONSECUTIVE VERIFIED CASES DURING THE DECADE 1968-1977 [J].
BROWN, P ;
CATHALA, F ;
SADOWSKY, D ;
GAJDUSEK, DC .
ANNALS OF NEUROLOGY, 1979, 6 (05) :430-437
[4]   NEUROPATHOLOGICAL DIAGNOSTIC-CRITERIA FOR CREUTZFELDT-JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES) [J].
BUDKA, H ;
AGUZZI, A ;
BROWN, P ;
BRUCHER, JM ;
BUGIANI, O ;
GULLOTTA, F ;
HALTIA, M ;
HAUW, JJ ;
IRONSIDE, JW ;
JELLINGER, K ;
KRETZSCHMAR, HA ;
LANTOS, PL ;
MASULLO, C ;
SCHLOTE, W ;
TATEISHI, J ;
WELLER, RO .
BRAIN PATHOLOGY, 1995, 5 (04) :459-466
[5]   PSYCHIATRIC PHENOMENA IN ALZHEIMERS-DISEASE .1. DISORDERS OF THOUGHT CONTENT [J].
BURNS, A ;
JACOBY, R ;
LEVY, R .
BRITISH JOURNAL OF PSYCHIATRY, 1990, 157 :72-76
[6]   CLINICAL HETEROGENEITY AND UNUSUAL PRESENTATIONS OF CREUTZFELDT-JAKOB-DISEASE IN JEWISH PATIENTS WITH THE PRNP CODON 200 MUTATION [J].
CHAPMAN, J ;
BROWN, P ;
GOLDFARB, LG ;
ARLAZOROFF, A ;
GAJDUSEK, DC ;
KORCZYN, AD .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1993, 56 (10) :1109-1112
[7]   ORGANIC DELUSIONS - PHENOMENOLOGY, ANATOMICAL CORRELATIONS, AND REVIEW [J].
CUMMINGS, JL .
BRITISH JOURNAL OF PSYCHIATRY, 1985, 146 (FEB) :184-197
[8]  
ESMONDE TFG, 1994, THESIS TRINITY COLL
[9]   PSYCHIATRIC PRESENTATION OF CREUTZFELDT-JAKOB DISEASE - A CASE-REPORT [J].
KESHAVAN, MS ;
LISHMAN, WA ;
HUGHES, JT .
BRITISH JOURNAL OF PSYCHIATRY, 1987, 151 :260-263
[10]  
MCMILLAN JF, 1984, THESIS EDINBURGH U U