B7.073 Psychiatric Symptoms and Signs in Neurologic Disease Flashcards
delusions
beliefs maintained steadfastly even in the face of evidence contradicting them incontrovertible
hallucinations
perceptions occurring in the absence of corresponding external or somatic stimuli
psychosis
hallucinations or delusions
without insight into pathologic nature
impaired reality testing
clear sensorium
alert
attentive
oriented
-if a patient has a clear sensorium, psychosis is likely psychiatric
visual hallucinations
neurologic
auditory hallucinations
psychiatric
dementia
progressive cognitive impairment involving multiple cognitive domains interfering with function
- visual spatial skills
- executive function
- short term memory
- visual hallucinations
dementia in DLB
early impairment = attention, exec function, and visual spatial ability
memory often not affected early but will develop memory impairment over time
other features (non-dementia) of DLB
fluctuating cognition (pronounced variation in attention and alertness)
recurrent visual hallucinations
REM sleep behavioral disorder
features of parkinsonism
neuropathologic changes in DLB
widespread limbic and cortical lewy bodies
aggregates of a-synuclein that involve the brainstem as well as cortical regions
loss of dopaminergic neurons in the substantia nigra
loss of cholinergic neurons in ventral forebrain nuclei
dopamine blocker sensitivity in DLB
loss of dopaminergic neurons
triggers or exacerbations in parkinsonism may be irreversible
increased risk of neuroleptic malignant syndrome
affects cognition and impairs attention and alertness
cognitive management of DLB
cholinesterase inhibitors (may worsen parkinsonism)
rivastigmine
donepezil
memantine
psychosis management of DLB
atypical antipsychotics with the least EPS side effects
avoid typicals as they will worsen parkinsonism
management of parkinsonism in DLB
carbidopa/levodopa (can worsen hallucinations and confusion)
avoid dopamine agonist
rapidly progressive dementia
dementia developing over < 1 year
what is CJD
rare sporadic disease characterized by brain prion protein crystallization
rapidly progressive dementia associated with other neurologic signs including myoclonus
death usually within 6 months of onset
types of CJD
sporadic
hereditary
variant
MRI findings in CJD
restricted diffusion
subcortical gray and cortical gray
CSF findings in CJD
14-3-3 proteins
- family of regulatory proteins
- elevated amounts found in CSF
- proteins spill into CSF with rapid neuronal death
what is RT-QuIC
real time quaking induced conversion
- detection of prion in CSF
- more specific
perceptual symptoms of schizophrenia
delusions
halucinations
executive symptoms of schizophrenia
disorganized speech
gross disorganized behavior
findings in anti-NMDA encephalitis
high protein on CSF
teratoma on abdominal ultrasound
NMDA receptor Ab (1:80) in serum and (1:5) in CSF
clinical course of anti-NMDA encephalitis
- viral prodrome
- psych symptoms
- neuro complications
- prolonged deficits