| Literature DB >> 2405293 |
P Brown1, F Jannotta, C J Gibbs, H Baron, D C Guiroy, D C Gajdusek.
Abstract
We report the case of a 73-year-old patient in whom a diagnosis of Creutzfeldt-Jakob disease, suggested by the clinical course, was verified by the neuropathologic finding of widespread spongiform change and astrogliosis, the presence of proteinase-resistant protein in brain extracts, and the experimental transmission of spongiform encephalopathy to primates inoculated with brain tissue. However, neuropathologic examination also revealed a profusion of senile and neuritic plaques and neurofibrillary tangles that reacted with antibody to the amyloid beta-protein characteristic of Alzheimer's disease, but not with antibody to the scrapie amyloid protein characteristic of Creutzfeldt-Jakob disease.Entities:
Mesh:
Year: 1990 PMID: 2405293 DOI: 10.1212/wnl.40.2.226
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910