Iatrogenic Creutzfeldt-Jakob disease with florid plaques

Brain Pathology

Volumn 13, Issue 3, 2003, Pages 245-249

  Kretzschmar, Hans A ^a   Sethi, Shneh ^a   Földvári, Zsuzsanna ^a   Windl, Otto ^a   Querner, Veronika ^a   Zerr, Inga ^b   Poser, Sigrid ^b  

^a UNIVERSITY OF MUNICH   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN; AMYLOID; CELL SURFACE RECEPTOR; GLYCOFORM SPECIFIC RECEPTOR, HUMAN; INFECTIOUS AMYLOID PRECURSOR PROTEIN; LECTIN; PRNP PROTEIN, HUMAN; PROTEIN PRECURSOR; PROTEINASE K;

ADULT; AGED; ARTICLE; AUTOPSY; BRAIN; BRAIN TISSUE; CASE REPORT; CLINICAL FEATURE; CREUTZFELDT JAKOB DISEASE; DEATH; DURA MATER; FEMALE; GENETICS; HUMAN; IATROGENIC DISEASE; INCUBATION TIME; MALE; NEUROPATHOLOGY; PRION DISEASE; WESTERN BLOTTING; BRAIN CORTEX; DRUG EFFECT; METABOLISM; METHODOLOGY; MIDDLE AGED; PATHOLOGY; PRION; REVIEW; TRANSPLANTATION;

AGED; AMYLOID; BLOTTING, WESTERN; CEREBRAL CORTEX; CREUTZFELDT-JAKOB SYNDROME; DURA MATER; ENDOPEPTIDASE K; FEMALE; HUMANS; LECTINS, C-TYPE; MALE; MIDDLE AGED; PRIONS; PROTEIN PRECURSORS; PRPSC PROTEINS; RECEPTORS, CELL SURFACE;

EID: 0043128815     PISSN: 10156305     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1750-3639.2003.tb00025.x     Document Type: Article

References (15)

1. Asante EA, Linehan JM, Desbruslais M, Joiner S, Gowland I, Wood AL, Welch J, Hill AF, Lloyd SE, Wadsworth JDF, Collinge J (2002) BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein. EMBO J 21:6358-6366.
2. Brown P, Preece M, Brandel JP, Sato T, McShane L, Zerr I, Fletcher A, Will RG, Pocchiari M, Cashman NR, d'Aignaux JH et al (2000) Iatrogenic Creutzfeldt-Jakob disease at the millennium. Neurology 55:1075-1081.
3. Collinge J, Sidle KCL, Meads J, Ironside J, Hill AF (1996) Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature 383:685-690.
4. Deslys JP, Lasmezas CI, Streichenberger N, Hill A, Collinge J, Dormont D, Kopp N (1997) New variant Creutzfeldt-Jakob disease in France. Lancet 349:30-31.
5. Katayama S, Watanabe K, Noda H, Tokinobu H, Yamamura Y, Jin C et al (2002) A case of sudden death six months after onset of Creutzfeldt-Jakob disease with florid plaques after dural graft. Neuropathology 22:A 17.
6. Kimura N, Kawai M (2002) Creutzfeldt-Jakob disease with Kuru and florid plaques after cadaveric dura mater grafting. Neuropathology 22:A17.
7. Kopp N, Streichenberger N, Deslys JP, Laplanche JL, Chazot G (1996) Creutzfeldt-Jakob disease in a 52-year-old woman with florid plaques. Lancet 348:1239-1240.
8. Parchi P, Capellari S, Chen SG, Petersen RB, Gambetti P, Kopp N, Brown P, Kitamoto T, Tateishi J, Giese A, Kretzschmar HA (1997) Typing prion isoforms. Nature 386:232-233.
9. Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AAF, Trojanowski JQ, Petersen RB, Gambetti P (1996) Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 39:767-778.
10. Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S et al (1999) Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46:224-233.
11. Shimizu S, Hoshi K, Muramoto T, Homma M, Ironside JW, Kuzuhara S, Sato T, Yamamoto T, Kitamoto T (1999) Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting. Arch Neurol 56:357-362.
12. Takashima S, Tateishi J, Taguchi Y, Inoue H (1997) Creutzfeldt-Jakob disease with florid plaques after cadaveric dural graft in a Japanese woman. Lancet 350:865-866.
13. Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A, Poser S, Pocchiari M, Hofman A, Smith PG (2002) A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 347:921-925.
14. Will RG, Zeidler M, Stewart GE, Macleod MA, Ironside JW, Cousens SN, Mackenzie J, Estibeiro K, Green AJE, Knight RSG (2000) Diagnosis of new variant Creutzfeldt-Jakob disease. Ann Neurol 47:575-582.
15. Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA (1999) Molecular genetics of human prion diseases in Germany. Hum Genetics 105:244-252.