Path X Flashcards

1
Q

common mycotic infection of nervous system

A

aspergillosis

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2
Q

spores in lungs

A

aspergillosis

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3
Q

spread of aspergillosis

A

hematogenous

direct invasion

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4
Q

what does aspergillosis cause in brain

A

hemorrhagic infarcts and abscesses

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5
Q

prognosis aspergillosis

A

high mortality with appropriate therapy

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6
Q

aspergillosis affects what parts of brain

A

meninges and parenchyma

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7
Q

45 degree branching on histo from vascular wall section

A

aspergillosis

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8
Q

how do amoebic abscesses happen

A

enteric viruses
gets to cerebrum through nasal cavity
can get from swimming in fresh water bodies

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9
Q

most common parasitic infection of CNS leading cause epilepsy worldwide

A

neurocysticercosis

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10
Q

how do people acquire neurocysticercosis

A

pork meat

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11
Q

what occurs in neurocysticercosis

A

inflammatory after parasites death
eventually calcifies
focal or generalized seizures, papilledema, HA, vomiting and ataxia, vertigo, focal motor and sensory deficits, dementia, acute hydrocephalus and occasionally sudden death

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12
Q

multiple cysts through all of the parenchyma of brain

A

neurocysticercosis

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13
Q

cysts inside the ventricles of brain

A

neurocysticercosis

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14
Q

CD 4 count <100

A

lymphoma, EBV and DLBCL

toxoplasmosis

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15
Q

CD4 count <50

A

cryptococcus

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16
Q

imaging show multiple ring enhancing lesions

A

toxo

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17
Q

type of dementia in CJD

A

subacute progressive dementia

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18
Q

prions

A

proteinaceous infectious agents

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19
Q

presentation CJD

A

subacutely progressive dementia, often characteristic EEG changes and CSF findings
very long latent period
no Tx

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20
Q

prion precursor protein encoded by what gene

A

PRNP

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21
Q

PrPc

A

normal protein

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22
Q

PrPsc

A

abnormal protein, protease resistant

23
Q

human prion diseases

A

CJD
kuru
grestmann-straussler scheinker syndrome
fatal familial insomnia

24
Q

types of CJD

A

sporadic
familial
iatrogenic
variant

25
kuru
was from new guinea natives from eating brains of dead people
26
Gerstmann Straussler Scheinker syndrome GSS
autosomal dominant slowly progressive ataxia and dementia | widespread PrPtse amyloid plaques throughout CNS
27
fatal familial insomnia
autosomal dominant disorder with pathological lesions in thalamus
28
alpha pleated sheet prion
normal Prc
29
beta pleated sheet prion
Pr sc abnormal prion
30
what happens with one Pr sc prion
spreads
31
spongiosis and vacuolization on histo of brain
CJD | "spongioform degeneration"
32
how do prions cause neuronal death
stop normal transport in neurons
33
how are types of CJD distinguished
western blot of CSF
34
mad cow disease
CJD
35
anti NMDA R encephalitis
autoimmune encephalitis
36
What neurodegenerative diseases cause dementia
alzheimers parkinsons diffuse lewy body dementia huntingtons
37
alzheimers attack what part of brain
corticobasal degeneration cortical frontotemporal dementia
38
parkinsons attacks what part of brain
midbrain idiopathic post infectious
39
huntingtons affects what part of brain
caudate
40
CAG repeat syndromes
spinocerebellar degenerations | spinocerebellar ataxias and friedreichs ataxia
41
ALS attacks what in brain
motor system
42
what can cause cellular damage in brain
free radicals DNA damage and repair excitotoxicity BBB dysfunction mitochondrial dysfunction with energy depletion protein truncation with dysfunction/misfolding and/or accumulation
43
alpha 1 antitrypsin deficiency is caused by
caused by protein misfolding
44
endoplasmic reticulum dilated from aggregates of misfolded protein
alpha1 antitrypsin deficiency
45
the misfolded proteins in alpha1 antitrypsin deficiency cause what
apoptosis
46
common feature of several neurodegenerative conditions
``` beta amyloid tau TDP43 synuclein huntingtin prion protein ```
47
beta amyloid collects in what diseases
alzheimer disease | cerebral amyloid angiopathy
48
tau collects in what diseases
alzheimers frontotemporal lobar degeneration picks disease progressive supranuclear palsy, corticobasal degeneration
49
TDP43 collects in
frontotemporal lobar degeneration | some forms of ALS
50
synuclein collects in
parkinsons | dementia with lewy bodies disease, multiple system atrophy
51
huntington collects in
huntingtons
52
prio protein diseases
CJD vCJD GSS FFI
53
alzheimer disease protein build up
beta amyloid | tau