Med/Psych Update

Evaluating for conversion disorder: When to suspect Creutzfeldt-Jakob disease

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References

Table 2

Distinguishing features of Creutzfeldt-Jakob disease

Sporadic CJDADDLBDFTD-MND
Time courseRapid progression (median survival 4 to 5 months)Insidious onset; progressive declineInsidious onset; progressive declineMay experience rapid course to death
Age at onsetAge 50 to 70Incidence increases with age (usual onset age 65 to 85)Older (age ~80)Young age at onset
EEG findingsPeriodic atypical triphasic waves; GPEDsNormal or diffuse abnormalitiesRarely atypical triphasic wavesIncreased slow activity, decreased fast activity
MRI findingsRestricted diffusionGeneralized atrophyGeneralized atrophyFrontal atrophy
AD: Alzheimer’s disease; CJD: Creutzfeldt-Jakob disease; DLBD: diffuse Lewy body dementia; EEG: electroencephalography; FTD-MND: frontotemporal dementia with motor neuron disease; GPEDs: generalized periodic epileptiform discharges
Source: References 7,8,19

Related Resources

National Institute of Neurological Disorders and Stroke. Creutzfeldt-Jakob disease fact sheet. www.ninds.nih.gov/disorders/cjd/detail_cjd.htm.

Centers for Disease Control and Prevention. About CJD. www.cdc.gov/ncidod/dvrd/cjd.

Drug Brand Names

Chlorpromazine • Thorazine, Largactil

Quinacine • Atabrine

Disclosure

Dr. Gagliardi reports no financial relationship with any company whose products are mentioned in this article or with manufacturers of competing products.

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