Basic Science › Neuropathology

Introduction to Neuropathology

Introduction to Neuropathology

What You'll Learn

  • A systematic way to read any neuropathology slide — orient, low power, high power, name the pattern, then order stains
  • When to use low vs high magnification
  • The core stains and a decision guide for which stain answers which question
  • How tissue is prepared (permanent / frozen / smear) and the artifacts that fool you

What You'll Learn

PowerWhat it's forWhat you read
Low (2–10×)Screening & architectureOrientation, lesion distribution (focal/diffuse/perivascular/laminar), cellularity, demarcation, normal-vs-abnormal comparison
High (20–40×)Cytology & detailNuclear atypia, mitoses, microvascular proliferation, inclusions, organisms, single-cell reactions (red neurons, chromatolysis)

Histochemical Stains

StainTargetKey use
H&EGeneral morphologyNuclei blue, cytoplasm pink; red neurons bright eosinophilic
Nissl (cresyl violet)Neuronal rough ERIdentifies neurons; Nissl dissolves in chromatolysis
Luxol fast blueMyelinMyelin blue; pale = demyelination/dysmyelination
Silver (Bielschowsky/Bodian)Axons, tangles, plaquesArgyrophilic; Alzheimer pathology
Congo red / thioflavinAmyloidApple-green birefringence (polarized light)
PASGlycogen, fungi, BMLafora bodies, corpora amylacea, fungi
GMS / mucicarmineFungiGMS black; mucicarmine = Cryptococcus capsule
Ziehl-NeelsenAcid-fast bacilliTuberculosis (red bacilli)
Prussian blue (Perls)Iron / hemosiderinOld hemorrhage, remote infarct, siderosis
Gomori trichromeMuscle / mitochondriaRagged red fibers; nemaline rods
Masson-FontanaMelaninMetastatic melanoma; neuromelanin
von Kossa / AlizarinCalciumCalcification (psammoma bodies, Fahr)
Oil Red ONeutral lipidFrozen tissue only; foamy macrophages, myelin debris
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