Prion diseases

被引:0
作者
Leemans, Michelle [1 ]
机构
[1] Natl Hosp Neurol & Neurosurg, London, England
关键词
Blood transfusions; Creutzfeldt-Jakob disease; endoscopes; prion disease; transmissible spongiform encephalopathies; CREUTZFELDT-JAKOB-DISEASE;
D O I
暂无
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The prion diseases, or transmissible spongiform encephalopathies (TSEs), are a group of neurodegenerative diseases. They are caused by an abnormal form of a naturally occurring cellular protein, known as prion protein. All prion diseases are fatal and without cure. Although all are rare, interest has increased over the last 20 years due to the appearance of a new prion disease called variant Creutzfeldt-Jakob disease. This disease is transmissible via medical devices and blood and therefore has implications for the anaesthetist, especially where blood transfusions and the use of airway devices and fibreoptic equipment are concerned.
引用
收藏
页码:56 / 59
页数:4
相关论文
共 7 条
  • [1] Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey
    Clewley, Jonathan P.
    Kelly, Carole M.
    Andrews, Nick
    Vogliqi, Kelly
    Mallinson, Gary
    Kaisar, Maria
    Hilton, David A.
    Ironside, James W.
    Edwards, Philip
    McCardle, Linda M.
    Ritchie, Diane L.
    Dabaghian, Reza
    Ambrose, Helen E.
    Gill, O. Noel
    [J]. BRITISH MEDICAL JOURNAL, 2009, 338 : 1316
  • [2] Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
    Gill, O. Noel
    Spencer, Yvonne
    Richard-Loendt, Angela
    Kelly, Carole
    Dabaghian, Reza
    Boyes, Lynnette
    Linehan, Jacqueline
    Simmons, Marion
    Webb, Paul
    Bellerby, Peter
    Andrews, Nick
    Hilton, David A.
    Ironside, James W.
    Beck, Jon
    Poulter, Mark
    Mead, Simon
    Brandner, Sebastian
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2013, 347
  • [3] The same prion strain causes vCJD and BSE
    Hill, AF
    Desbruslais, M
    Joiner, S
    Sidle, KCL
    Gowland, I
    Collinge, J
    Doey, LJ
    Lantos, P
    [J]. NATURE, 1997, 389 (6650) : 448 - 450
  • [4] Prevalence of lymphoreticular prion protein accumulation in UK tissue samples
    Hilton, DA
    Ghani, AC
    Conyers, L
    Edwards, P
    McCardle, L
    Ritchie, D
    Penney, M
    Hegazy, D
    Ironside, JW
    [J]. JOURNAL OF PATHOLOGY, 2004, 203 (03) : 733 - 739
  • [5] Lymphocyte contamination of laryngoscope blades - a possible vector for transmission of variant Creutzfeldt-Jakob disease
    Hirsch, N
    Beckett, A
    Collinge, J
    Scaravilli, F
    Tabrizi, S
    Berry, S
    [J]. ANAESTHESIA, 2005, 60 (07) : 664 - 667
  • [6] Ironside JW, 2012, FOLIA NEUROPATHOL, V50, P50
  • [7] Population Screening for Variant Creutzfeldt-Jakob Disease Using a Novel Blood Test Diagnostic Accuracy and Feasibility Study
    Jackson, Graham S.
    Burk-Rafel, Jesse
    Edgeworth, Julie Ann
    Sicilia, Anita
    Abdilahi, Sabah
    Korteweg, Justine
    Mackey, Jonathan
    Thomas, Claire
    Wang, Guosu
    Schott, Jonathan M.
    Mummery, Catherine
    Chinnery, Patrick F.
    Mead, Simon
    Collinge, John
    [J]. JAMA NEUROLOGY, 2014, 71 (04) : 421 - 428