Creutzfeldt-Jakob disease with neuroleptic malignant syndrome

被引:0
作者
Ciauskaite, Julija [1 ]
Puleikyte, Ieva [1 ]
Jesmanas, Simonas [2 ]
Jurkeviciene, Giedre [1 ]
Vaitkus, Antanas [1 ]
Rastenyte, Daiva [1 ]
机构
[1] Lithuanian Univ Hlth Sci, Med Acad, Dept Neurol, Mickeviciaus Str 9, LT-44307 Kaunas, Lithuania
[2] Lithuanian Univ Hlth Sci, Med Acad, Dept Radiol, Kaunas, Lithuania
来源
CLINICAL CASE REPORTS | 2021年 / 9卷 / 08期
关键词
atypical antipsychotic medications; Creutzfeldt-Jakob disease; electroencephalography; magnetic resonance imaging; neuroleptic malignant syndrome; quetiapine; SENSITIVITY;
D O I
10.1002/ccr3.4699
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Creutzfeldt-Jakob disease (CJD) is a rare rapidly progressive fatal neurodegenerative disease. Neuroleptic malignant syndrome (NMS) is a complication of antipsychotic medications which may be used to treat neuropsychiatric symptoms of CJD. We present a case of a 51-year-old woman with CJD who developed NMS after being prescribed quetiapine.
引用
收藏
页数:7
相关论文
共 31 条
[1]  
[Anonymous], 2018, Diagnostic Criteria
[2]   Myoglobinuria, malignant hyperthermia, neuroleptic malignant syndrome and serotonin syndrome [J].
Bertorini, TE .
NEUROLOGIC CLINICS, 1997, 15 (03) :649-+
[3]   CREUTZFELDT-JAKOB DISEASE - CLINICAL ANALYSIS OF A CONSECUTIVE SERIES OF 230 NEUROPATHOLOGICALLY VERIFIED CASES [J].
BROWN, P ;
CATHALA, F ;
CASTAIGNE, P ;
GAJDUSEK, DC .
ANNALS OF NEUROLOGY, 1986, 20 (05) :597-602
[4]   MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease [J].
Carswell, Christopher ;
Thompson, Andrew ;
Lukic, Ana ;
Stevens, John ;
Rudge, Peter ;
Mead, Simon ;
Collinge, John ;
Hyare, Harpreet .
BMC NEUROLOGY, 2012, 12
[5]   Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease [J].
Collins, S. J. ;
Sanchez-Juan, P. ;
Masters, C. L. ;
Klug, G. M. ;
van Duijn, C. ;
Poleggi, A. ;
Pocchiari, M. ;
Almonti, S. ;
Cuadrado-Corrales, N. ;
de Pedro-Cuesta, J. ;
Budka, H. ;
Gelpi, E. ;
Glatzel, M. ;
Tolnay, M. ;
Hewer, E. ;
Zerr, I. ;
Heinemann, U. ;
Kretszchmar, H. A. ;
Jansen, G. H. ;
Olsen, E. ;
Mitrova, E. ;
Alperovitch, A. ;
Brandel, J. -P. ;
Mackenzie, J. ;
Murray, K. ;
Will, R. G. .
BRAIN, 2006, 129 :2278-2287
[6]  
Cumbler Ethan, 2009, Cases J, V2, P122, DOI 10.1186/1757-1626-2-122
[7]   Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation [J].
Eisenmenger, Laura ;
Porter, Marie-Claire ;
Carswell, Christopher J. ;
Thompson, Andrew ;
Mead, Simon ;
Rudge, Peter ;
Collinge, John ;
Brandner, Sebastian ;
Jager, Hans R. ;
Hyare, Harpreet .
JAMA NEUROLOGY, 2016, 73 (01) :76-84
[8]   Imaging of Creutzfeldt-Jakob Disease: Imaging Patterns and Their Differential Diagnosis [J].
Fragoso, Diego Cardoso ;
da Mota Goncalves Filho, Augusto Lio ;
Pacheco, Felipe Torres ;
Barros, Bernardo Rodi ;
Littig, Ingrid Aguiar ;
Nunes, Renato Hoffmann ;
Martins Maia Junior, Antonio Carlos ;
da Rocha, Antonio J. .
RADIOGRAPHICS, 2017, 37 (01) :233-256
[9]  
Geschwind Michael D, 2016, Continuum (Minneap Minn), V22, P510, DOI 10.1212/CON.0000000000000319
[10]   Sporadic Creutzfeldt-Jakob disease prion infection of human cerebral organoids [J].
Groveman, Bradley R. ;
Foliaki, Simote T. ;
Orru, Christina D. ;
Zanusso, Gianluigi ;
Carroll, James A. ;
Race, Brent ;
Haigh, Cathryn L. .
ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2019, 7 (1) :90