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Pathology · Systemic pathology: Pick disease
Sample itemA 58-year-old man develops disinhibition, apathy and language disturbance with relatively preserved memory early on. MRI shows severe, knife-edge atrophy of the frontal and anterior temporal lobes. Histology shows ballooned neurons and round intraneuronal inclusions. Which protein forms these inclusions?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Tau
Pick disease is a form of frontotemporal lobar degeneration in which round cytoplasmic Pick bodies composed of tau accumulate in neurons. Alzheimer disease also involves tau, but there memory loss comes first and amyloid plaques are present.
Option by option
A. Prion protein
Prion protein deposition causes spongiform change in Creutzfeldt-Jakob disease.
B. Tau (correct)
Correct. Pick bodies are composed of tau protein, and the disease is a frontotemporal tauopathy.
C. Beta-amyloid
Beta-amyloid forms the extracellular plaques of Alzheimer disease.
D. Alpha-synuclein
Alpha-synuclein forms Lewy bodies in Parkinson disease and dementia with Lewy bodies.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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