[Neuropathology of non conventional infectious agents or prions]

Pathol Biol (Paris). 1995 Jan;43(1):43-52.
[Article in French]

Abstract

The neuropathological diagnosis of infections by non conventional agents relies on four lesions: astrocytic gliosis (cell hypertrophy and proliferation) usually contrasting with absent mononuclear cell infiltrates (lymphocytes, monocytes-macrophages, and/or microglia) revealed by conventional techniques, and neuronal loss in the most affected areas are little specific findings. Amyloid plaques that are inconstantly found, and spongiosis of gray matter, a characteristic and very frequent finding, are most specific. PrP immunohistochemistry brings additional data. The main diagnostic difficulties are emphasized, and guidelines for Pathological studies are recalled.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Animals
  • Cattle
  • Creutzfeldt-Jakob Syndrome / diagnosis*
  • Creutzfeldt-Jakob Syndrome / pathology
  • Diagnosis, Differential
  • Encephalopathy, Bovine Spongiform / diagnosis*
  • Encephalopathy, Bovine Spongiform / pathology
  • Gerstmann-Straussler-Scheinker Disease / diagnosis*
  • Gerstmann-Straussler-Scheinker Disease / pathology
  • Humans
  • Kuru / diagnosis*
  • Kuru / pathology
  • Prion Diseases / diagnosis*
  • Prion Diseases / pathology