Prion disease: Difference between revisions
No edit summary |
ClaireLewis (talk | contribs) No edit summary |
||
| Line 27: | Line 27: | ||
*Evaluate for reversible/treatable causes of dementia | *Evaluate for reversible/treatable causes of dementia | ||
**CBC, B12, folate, thiamine | **CBC, B12, folate, thiamine | ||
**LFTs, BMP, TSH, [[Urinalysis]] | **[[LFTs]], BMP, TSH, [[Urinalysis]] | ||
**[[ECG]], [[CXR]] | **[[ECG]], [[CXR]] | ||
**ETOH, Utox, urine heavy metals | **ETOH, [[Utox]], urine heavy metals | ||
**RPR, ESR, ANA, HIV | **RPR, ESR, ANA, HIV | ||
**[[LP]] | **[[LP]] | ||
*MRI: | *[[brain MRI|MRI]]: | ||
**Areas of increased signal intensity bilaterally, mostly in caudate and putamen | **Areas of increased signal intensity bilaterally, mostly in caudate and putamen | ||
**Posterior thalamic hyperintensity | **Posterior thalamic hyperintensity | ||
| Line 40: | Line 40: | ||
==Management== | ==Management== | ||
*No specific treatment | *No specific treatment | ||
*Consider palliative care consult for symptom alleviation and support | *Consider [[palliative care]] consult for symptom alleviation and support | ||
==Disposition== | ==Disposition== | ||
Revision as of 22:39, 2 October 2019
Background
- Prions are misfolded proteinaceous particles
- Replicate exponentially by causing properly folded proteins to misfold
- Rapidly leads to neurodegeneration
- Universally fatal
- Transmissible forms:
- Variant CJD acquired by consuming diseased tissues of cows (e.g. human form of mad cow disease) or other humans (kuru)
- Iatrogenic (handling diseased corneas/brain or improperly disinfected equipment)
- Hereditary prion disease:
- Familial CJD: mutation in PRNP, which encodes prion protein
- Fatal familial insomnia
- Gerstmann-Sträussler-Scheinker syndrome
- Sporadic CJD: accounts for ~85% of cases, cause is unknown
Clinical Features
- Progressive dementia, behavioral changes, loss of cortical function over several months
- Myoclonus
- Extrapyramidal symptoms (hypokinesia)
- Cerebellar dysfunction- ataxia, dysarthria
- Coma
Differential Diagnosis
Dementia
- Degenerative
- Alzheimer's disease
- Huntington's disease
- Parkinson's disease
- Vascular
- Multiple infarcts
- Hypoperfusion (MI, profound hypotension)
- Subdural hematoma
- SAH
- Infectious
- Meningitis (sequelae of bacterial, fungal, or tubercular)
- Neurosyphilis
- Viral encephalitis (HSV, HIV), Creutzfeldt-Jakob disease
- Inflammatory
- SLE
- Demyelinating disease (e.g. multiple sclerosis)
- Neoplastic
- Primary brain tumor / metastatic disease
- Carcinomatous meningitis
- Paraneoplastic syndromes
- Traumatic
- Toxic
- ETOH
- Meds (anticholinergics, polypharmacy)
- Metabolic
- Psychiatric
- Depression (pseudodementia)
- Hydrocephalic
- Normal pressure hydrocephalus (communicating hydrocephalus)
- Noncommunicating hydrocephalus
Evaluation
- Not an ED diagnosis, as definitive diagnosis only possible by autopsy
- Evaluate for reversible/treatable causes of dementia
- MRI:
- Areas of increased signal intensity bilaterally, mostly in caudate and putamen
- Posterior thalamic hyperintensity
- EEG
- Usually nonspecific but abnormal
Management
- No specific treatment
- Consider palliative care consult for symptom alleviation and support