Frontotemporal Dementia Flashcards

1
Q

What is frontotemporal dementia?

A

A primary neurodegenerative condition characterised by progressive illness with behaviour changes and language problems

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2
Q

What are the risk factors for FTD?

A
  • Family history: mutations in MAPT gene or GRN gene (Autosomal dominant inheritance)
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3
Q

What is the pathophysiology of FTD?

A
  • Symmetrical atrophy of frontal lobes with some temporal lobe involvement
  • Histology shows Tau inclusion bodies and inclusions of FTLD-U
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4
Q

How does FTD present?

A
  • Behavioural changes including apathy, disinhibition, loss of empathy, decline in social conduct
  • Difficulty with speech including aphasia, language difficulty, object naming
  • Decline in planning and concentration
  • Short term memory problems
  • Behaviour/Speech problems normally picked up before memory decline which helps differentiate from other dementias
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5
Q

How should FTD be investigated?

A
  • Full screen: FBC, TFTs, LFTs, B12/Folate, U+Es
  • Cognitive testing: MMSE, MoCA
  • CT/MRI may show atrophy
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6
Q

How should FTD be managed?

A
  • Specialist management
  • Patient and family education
  • First line: non pharm therapy including group therapy
  • Benzos used for acute distress
  • SSRI for associated mood problems, irritability
  • Acetylcholinterase/Memantine NOT recommended
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