diagnostic criteria for new variant CJD
Last reviewed 01/2018
Diagnostic Criteria for Variant Creutzfeldt-Jakob Disease in the United States
Definite Variant CJD
Neuropathologic examination of brain tissue is required to confirm a diagnosis of variant CJD. The following confirmatory features should be present.
- a. Numerous widespread kuru-type amyloid plaques surrounded by vacuoles in both the cerebellum and cerebrum - florid plaques.
- b. Spongiform change and extensive prion protein deposition shown by immunohistochemistry throughout the cerebellum and cerebrum
Suspected Variant CJD
- a. Current age or age at death <55 years (a brain autopsy is recommended, however, for all physician - diagnosed CJD cases).
- b. Psychiatric symptoms at illness onset and/or persistent painful sensory symptoms (frank pain and/or dysesthesia).
- c. Dementia, and development > 4 months after illness onset of at least two of the following five neurologic signs: poor coordination, myoclo nus, chorea, hyperreflexia, or visual signs. (If persistent painful sensory symptoms exist, > 4 months delay in the development of the neurologic signs is not required).
- d. A normal or an abnormal EEG, but not the diagnostic EEG changes often seen in classic CJD
- e. Duration of illness of over 6 months.
- f. Routine investigations of the patient do not suggest an alternative, non-CJD diagnosis.
- g. No history of receipt of cadaveric human pituitary growth hormone or a dura mater graft.
- h. No history of CJD in a first degree relative or prion protein gene mutation in the patient
NOTE
- 1)If a patient has the typical bilateral pulvinar high signal on MRI scan,
a suspected diagnosis of variant CJD requires the presence of a progressive
neuropsychiatric disorder, d, e, f and g of the above criteria, and four of
the following five criteria: 1) early psychiatric symptoms (anxiety, apathy,
delusions, depression, withdrawal); 2) persistent painful sensory symptoms
(frank pain and/or dysesthesia); 3) ataxia; 4) myoclonus or chorea or dystonia;
and 5) dementia
- 2). A history of possible exposure to bovine spongiform encephalopathy (BSE) such as residence or travel to a BSE-affected country after 1980 increases the index of suspicion for a variant CJD diagnosis.
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