Neuropathology Flashcards

(35 cards)

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
how is spongiform encephalopathy safety precaution
prolonged autoclaving under high pressure and temperature, disposable instruments, surfaces treated with hypochlorite
26
what are some prion disorders
CJD - sporadic, familial, variant, GSS disease, Kuru fatal insomnia - sporadic and familial
27
pathology of prion diseases
spongiform vacuolar change in grey matter, gliosis, neuronal loss with abnormal folded prion protein, astrocyte proliferation
28
what are the neuromuscular disorders
congenital myopathies, muscular dystrophies, inflammatory muscle diseases, neurogenic diseases, drug induced or metabolic
29
how are muscle biopsies divided
1. frozen in isopentane, cooled in liquid nitrogen 2. frozen for DNA studies 3. fixed in glutaraldehyde for EM 3. fixed in formalin for paraffin sections
30
what are the inflammatory myopathies
polymyositis, dermatomyositis, inclusion body myositis
31
what is polymyositis
proximal painful weakness eg SLE
32
what is dermatomyositis
facial rash associated with malignancy in 15% of cases
33
what are the most common primary CNS tumour in adults
gliomas followed by meningiomas
34
do CNS tumours metastasise to other organs
almost never
35
what are oligodendrogliomas
slow growing neoplasms, cause epileptic seizures and headache