Intro to neuropsychiatry Flashcards

1
Q

What symptoms in dementia are generally considered to be the major source of caregiver stress?

A

Neuropsychiatric symptoms / BPSD

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2
Q

What lobes in Alzheimer’s are most commonly attacked first?

A

Temporal and parietal lobes

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3
Q

What is the characteristic sign of Lewy Body dementia that differentiates it from Alzheimer’s?

A
  • Well formed visual hallucinations

- Systematised dellusions (very detailed and well formed)

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4
Q

What features are essential for a diagnosis of Lewy body dementia?

A

2 of these 3:

  • Fluctuating cognition with pronounced variations in attention and alertness
  • Recurrent visual hallucinations well formed and detailed
  • Spontaneous motor features of parkinsonism
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5
Q

A diagnosis of Lewy Body dementia is less likely in the presence of what?

A
  • Stroke disease, evidnet as focal neurological signs or brain damage
  • Evidence on physical examination and investigation of any physical illness or other brain disorder sufficient to account for the clinical picture
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6
Q

What symptoms are associated with Alzheimer’s?

A
  • Plateaus in the course of progression of the illness
  • Associated symptoms of:
  • Depression
  • Insomnia
  • Incontinance
  • Dellusions
  • Illusions
  • Hallucinations
  • Catastrophic verbal, emotional, or physical outbursts
  • Sexual disorders
  • Weight loss
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7
Q

What are features of Alzheimer’s that make the diagnosis uncertain or unlikely?

A
  • Sudden, apoplectic onset
  • Focal neurological findings such as hemiparesis, sensory loss, visual field deficits, and incoordination early in the course of the illness
  • Seizures or gait disturbances at the onset or very early in the course of the illness
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8
Q

What are the central features required for a diagnosis of Lewy Body Dementia?

A
  • Progressive cognitive decline of sufficient magnitude to interfere with normal social or occupational function
  • Prominent or persistent memory impairment may not necessarily occur in the early stages but is usually evident with progression
  • Deficits on tests of attention and of frontal subcortical skills may be especially prominent
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9
Q

What disease is highly corolated with Lewy Body dementia?

A

Parkinson’s

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10
Q

What is the difference between Parkinson’s or Lewy Body dementia?

A
  • Parkinson’s patients present with motor symptoms first which then progress to parkinson’s dementia.
  • More pronounced cortical atrophy, elevated cortical and limbic in Lewy body pathologies
  • Higher A beta and tau loads in cortex and striatum in Lewy body compared to Parkinson’s
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11
Q

What symptoms does fronto-temporal dementia present with?

A
  • Speech
  • Behavioural symptoms associated with frontal lobe damage (early loss of social awareness, hygiene, unrestrained sexuality, hyprorality, impulsiveness, early loss of insight into the fact that the altered conditions are due to pathological changes)
  • Depression, anxiety, excessive sentimentality, suicidal and fixed ideation, delusion
  • Hypochondriasis, bizarre somatic preoccupation
  • Emotional unconcern (emotional indifference and remoteness, lack of empathy)
  • Amimia
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12
Q

What dementia is the patient generally thought to have when unable to diagnose any other dementia?

A

Vascular dementia

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13
Q

What is pseudobulbar palsy?

A

Personality and mood changes but are disconnected to facial muscles (e.g laughing whilst being upset and telling a sad story)
- Often seen in vascular dementia

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14
Q

What percentage of Motor neuron disease patients have major depressive disorder?

A

~ 50% (likely to reflect cortical damage, not just reaction to disability)

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15
Q

What can Motor neuron disease cause?

A
  • Mania - e.g oribitofrontal prefrontal cortex-impulsivity, mood lability, personality changes seen in mania
  • Pseudobulbar affect - disconnect between mood and affect
  • Psychosis 2-3x more common in MS patients compared to general population e.g medial temporal damage
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16
Q

What is the classic imaging sign of huntington’s?

A

Enlargement of lateral ventricles (due to degeneration of caudate nucleus and putamen)

17
Q

What are some symptoms of Huntington’s

A
  • Early depression and behavioural disturbances common - especially irritability, apathy, anxiety, dysphoria and agitation - independent of cognitive and motor aspects
  • Psychotic symptoms rare
  • Insight retained until late stages
18
Q

What is the suicide rate among those with Huntington’s?

A

~ 10%

19
Q

Cognitive and behavioural deficits are present in what percentage of Motor neuron diseases?

A

~ 50%

- Executive function, social and language deficits - fronto temporal type dementia

20
Q

What type of Dementia does motor neuron disease have a genetic overlap with?

A

Trinucleotide expansion in C9orf72

21
Q

What are synonyms of functional neurological disorders?

A
  • Functional movement disorder
  • Convension disorder
  • Psychogenic seizures / movement disorder
  • Dissociative seizures / motor disorder
  • Non-epileptic seizures
    Occur in about 1/4 of neurology clinic patients
22
Q

What is a functional neurological disorder?

A
  • Problem with the functionong of the nervous system and how the brain and body sends and/or receives signals, rather than a structural disease process such as multiple sclerosis or stroke
  • Symptoms are real, often fluctuate
  • Not entirely or always psychological
23
Q

What does imaging usually find in functional neurological disorders?

A
  • Imaging usually normal

- fMRI: hyperconnectivity between caudate, amygdala, prefrontal and sensorimotor areas

24
Q

WHat can be the causes of functional neurological disorders?

A
  • Past trauma
  • Stress
  • Migraine
  • Physical injury
  • Infection
25
Q

What are the treatments for functional neurological disorders?

A
  • Often treated just like neurological disorders
  • Physiotherapy
  • Speech therapy
  • Cognitive behavioral therapy