Neuropathology Flashcards

1
Q

what are the 9 main causes of CNS diseases

A

congenital, inflammatory, neurodegenerative, vascular, tumours, metabolic, immune, traumatic, toxic

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2
Q

immune cause of CNS disease

A

multiple sclerosis

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3
Q

congenital causes of CNS diseases

A

malformations, hydrocephalus

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4
Q

function of the cortex

A

cognitive

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5
Q

function of the basal ganglia

A

movement

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6
Q

function of the brainstem

A

cranial nerve function, cardiac/respiratory control

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7
Q

function of the cerebellum

A

balance, smoothness of movement

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8
Q

function of the spinal cord

A

motor supply to limbs, sensory relay to brain

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9
Q

what is the composition of the brain

A

white matter and grey matter

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10
Q

what is grey matter composed of

A

neurons, glia, blood vessels

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11
Q

what is white matter composed of

A

CNS axons, myelin, glial cells, blood vessels

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12
Q

what is dementia

A

acquired global impairment of intellect, personality and memory without impairment of consciousness

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13
Q

neurodegenerative diseases

A

alzheimers, fronto temporal lobar degeneration, parkinsons, motorneurone, huntingtons chorea, prion disease

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14
Q

clinical signs of alzheimers disease

A

memory loss, language difficulty, general tasks

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15
Q

survival of alzheimers

A

8 years on average, death from bronchopneumonia/ inanition

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16
Q

alzheimer disease pathology

A

atropy, thin cortex, dilated ventricles, neuritic plaques

17
Q

microscopic pathology of alzheimers disease

A

amyloid deposits in grey matter as plaques, also arteries of cerebral cortex
neuritic plaques made up of degenerated neuritic dendites
neurofibrillary tangles

18
Q

pathogenesis of alzheimers

A

autosomal dominant in 10%
Chr 21 - mutation in amyloid precursor protein gene
Chr 14 - mutation in presenilin 1 gene

19
Q

who is most affected by fronto temporal lobar degeneration

A

all ages, often younger adults

20
Q

symptoms of FTLD

A

personality change, behavioral disorder, speech and movement disorder, intellectual deterioration

21
Q

what is parkinsons disease

A

degeneration of dopaminergic system

22
Q

pathology of parkinsons

A

loss of pigmented cells in S Nigra, Lewy bodies in SN neurones

23
Q

pathology of parkinsons

A

loss of pigmented cells in S Nigra, Lewy bodies in SN neurones

24
Q

treatment of parkinsons

A

L dopa improves symptoms

25
Q

how is spongiform encephalopathy safety precaution

A

prolonged autoclaving under high pressure and temperature, disposable instruments, surfaces treated with hypochlorite

26
Q

what are some prion disorders

A

CJD - sporadic, familial, variant,
GSS disease, Kuru
fatal insomnia - sporadic and familial

27
Q

pathology of prion diseases

A

spongiform vacuolar change in grey matter, gliosis, neuronal loss with abnormal folded prion protein, astrocyte proliferation

28
Q

what are the neuromuscular disorders

A

congenital myopathies, muscular dystrophies, inflammatory muscle diseases, neurogenic diseases, drug induced or metabolic

29
Q

how are muscle biopsies divided

A
  1. frozen in isopentane, cooled in liquid nitrogen
  2. frozen for DNA studies
  3. fixed in glutaraldehyde for EM
  4. fixed in formalin for paraffin sections
30
Q

what are the inflammatory myopathies

A

polymyositis, dermatomyositis, inclusion body myositis

31
Q

what is polymyositis

A

proximal painful weakness eg SLE

32
Q

what is dermatomyositis

A

facial rash associated with malignancy in 15% of cases

33
Q

what are the most common primary CNS tumour in adults

A

gliomas followed by meningiomas

34
Q

do CNS tumours metastasise to other organs

A

almost never

35
Q

what are oligodendrogliomas

A

slow growing neoplasms, cause epileptic seizures and headache