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Radiology · Neuroimaging: subacute sclerosing panencephalitis
Sample itemA 12-year-old boy who had measles in infancy has progressive intellectual decline and myoclonic jerks. EEG shows periodic high-voltage complexes, and MRI shows asymmetric periventricular and subcortical white matter T2 hyperintensity. What is the diagnosis?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Subacute sclerosing panencephalitis
SSPE is a delayed measles-virus encephalitis causing progressive dementia, myoclonus and periodic EEG complexes, with posterior-predominant white matter signal change on MRI. ADEM is monophasic after infection or vaccination, Wernicke affects the mamillary bodies and thalami, and PML affects immunosuppressed adults.
Option by option
A. Acute disseminated encephalomyelitis
ADEM is monophasic, appears soon after an infection and does not progress for years.
B. Wernicke encephalopathy
Wernicke encephalopathy is nutritional and involves medial thalami and mamillary bodies.
C. Subacute sclerosing panencephalitis (correct)
Correct. Measles exposure, myoclonus, periodic EEG and white matter change indicate SSPE.
D. Progressive multifocal leukoencephalopathy
PML occurs in immunosuppressed adults and is not tied to prior measles.
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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