Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease

Ann Neurol. 2004 Feb;55(2):294-6. doi: 10.1002/ana.20038.

Abstract

Currently, definite peripheral markers for the in vivo diagnosis of sporadic Creutzfeldt-Jakob disease (CJD) are not available. Here, we report the presence of pathological prion protein in the olfactory mucosa of a case with sporadic Creutzfeldt-Jakob disease. Prion protein immunoreactivity was detected in an olfactory biopsy performed 45 days after the disease onset, suggesting that the involvement of olfactory epithelium is an early event in sporadic Creutzfeldt-Jakob disease.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • Brain Chemistry
  • Creutzfeldt-Jakob Syndrome / pathology*
  • Creutzfeldt-Jakob Syndrome / physiopathology
  • Female
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Olfactory Mucosa / metabolism*
  • Olfactory Mucosa / pathology
  • PrPSc Proteins / metabolism*

Substances

  • PrPSc Proteins