10 Neuropathology (CNS infections) Flashcards

(39 cards)

1
Q

Name the 4 routes via which infectious agents can enter the CNS

A
  • hematogenous
  • direct implantation
  • local extension from adjacent site of infection
  • axoplasmic transport along peripheral nerve axons
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2
Q

Bacteria and yeast most often cause what type of meningitis?

A

pyogenic or granulomatous

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3
Q

Hyphal forms of fungi most often cause ____ and _____

A

cerebritis

abscesses

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4
Q

T/F- bacterial is the most common type of CNS infection and results in meningitis more frequently than abscess

A

true

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5
Q

Viral infections usually cause what?

A

encephalitis, meningoencephalitis

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6
Q

Describe the CSF findings in bacterial pyogenic meningitis

A

many neutrophils
high protein
low glucose

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7
Q

Describe the clinical symptoms of bacterial pyogenic meningitis

A

headache
altered mental state-encephalopathy
increased intracranial pressure
seizures

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8
Q

What 2 organisms cause acute (purulent) meningitis in neonates

A

Group B strep

Listeria Monocytogenes

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9
Q

What 3 organisms cause acute meningitis in young children

A

N. meningitidis
Strep pneumoniae
H. influenzae (unvaccinated)

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10
Q

What 2 organisms cause acute meningitis in older children/adults?

A

Strep. pneumoniae

Neisseria meningitidis

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11
Q

T/F- in bacterial meningitis you’ll likely see pmns in leptomeninges

A

true

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12
Q

Name 2 complications of meningitis

A

infarcts

chronic hydrocephalus

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13
Q

Lymphocytic meningitis (aka aseptic/viral) is usually self limited. What will you see in the CSF?

A

lymphocytes
moderately high protein
Normal glucose

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14
Q

Name 2 most common causes of lymphocytic/aseptic meningitis

A

echovirus

coxsackie virus

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15
Q

Name 3 causes of chronic (granulomatous) meningitis

A
  1. M. tuberculosis/avium
  2. Yeast forms of fungi (cryptococcus, coccidioides, blastomyces)
  3. rarely sarcoidosis
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16
Q

What is a feared complication of chronic meningitis?

A

obliterative endarteritis leading to infarction of underlying brain

17
Q

chronic meningitis has a predilection for _____

A

base of brain

18
Q

What bacteria commonly cause cerebrates and abscess in the brain?

A

Anaerobic strep
Strep pneumoniae
Staph sp.

19
Q

What fungi cause cerebrates and abscess of the brain?

A

aspergillus
mucor
candida

20
Q

What protozoal infection can cause cerebrates and abscess of the brain?

21
Q

What is the most common method of pathogen “spread” leading to cerebritis and abscess?

A
Direct spread (50%)
hematogenous spread (25%)
22
Q

Rank the following from most to least common location of brain abscess: parietal, cerebellum, frontal

A

Frontal»parietal>cerebellum

23
Q

What is cerebritis?

A

focal infection/inflammation before an established abscess (with a wall) forms

24
Q

T/F- abscesses present as a ring enhancing lesion on CT

25
What type of pathogen (virus, bacteria, etc) is most often responsible for encephalitis?
viruses
26
Will you see microglial nodules and neuronophagia with viral encephalitis?
yes
27
Rabies: ____ body inclusion Herpes: ____ body inclusion
negri body | cowdry type A
28
What virus causes progressive multifocal leukoencephalopathy?
JC virus
29
In HIV encephalitis, you'll often see multinucleated giant cells located where?
around vessels
30
in PML you'll see bizarre, atypical ______ as well as intranuclear inclusions in ______ cells
1. astrocytes (reactive, not neoplastic) | 2. oligodendroglial cells
31
Is toxoplasmosis a ring enchancing lesion?
yes
32
In spongioform encephalopathy are the vacuoles in the white or gray matter?
gray
33
Classic triad of symptoms in prion diseases?
rapid dementia myoclonus periodic short wave activity on EEG
34
Are most cases of CJD sporadic or familial?
most are sporadic | only 10-15% familial
35
What chromosome is the normal gene for protease resistant prion protein on?
chrom20
36
Describe the pathogenesis of prion disease
- Disease occurs with conformational change of PrP 3D structure into ß-pleated sheet - Single pathogenic PrP can induce further protein conversions of wild type protein creating a chain reaction - PrP accumulates in and outside of cells in the form of amyloid
37
Is there a mutation that increase your risk for sporadic CJD?
Homozygosity for Met or Val at codon 129 increases risk of sporadic CJD
38
T/F- CJD brain will always show atrophy
false, may look normal or may show atrophy
39
Describe the microscopic appearance of CJD
Neuronal loss, gliosis, and spongiform change (often patchy), defined by small “punched out” vacuoles in gray matter (cortex ± deep nuclei)