spinal Disorders, brain abscess Flashcards

1
Q

causes of brain abscess / organisms?

A
  1. spread from contguous infection in the sinuses, mastoid air cells or otitis media
  2. bacteremia (esp pneumonia and endocaditis)
    organisms: staph, strep, gram (-) bacillim anaerobes (frequently mixed)
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2
Q

how to distinguish brain cancer from abscess

A
no way (not even on imaging study) --> only with biopsy
(cancer can give fever) --> also to determine the precise organism and its sensitivity
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3
Q

brain abscess - best initial test / most accurate

A
  • best initial: CT or MRI: ring or contrast enhancing lesions that will likely have surrounding edema and mass effect
  • most accurate: brain biopsy
  • LP: useless and contraindicated
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4
Q

brain abscess - treatment

A
  • empiric therapy with penicillin + metronidazole + ceftriaxone (or cefepime) is acceptable while waiting for results
  • if recent neurosurgery and risk risk of staph: vancomycin
  • avoid prolonged empiric therapy
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5
Q

anterior spinal artery infraction - manifestation + treatment

A
  1. loss of al function except the posterior column (position + vibration intact)
  2. flaccid paralysis below infraction
  3. loss of DTR at the level of the infraction
  4. loss of pain and Q
  5. extensor plantar response
  6. evolves plastic paraplegia several wks later
    - no specific treatment
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6
Q

sabacute combined degeneration of the Cord - causes and manifestation

A
  • from b12 def or neurosyphilis

- position and vibratory sensation are lost

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7
Q

vitamin B12 deficiency - spinal cord lesions

A

sabacute combined degeneration –> demyelination of dorsal column, lateral corticospinal tracts, and spinocerebellar tracts

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8
Q

vitamin B12 deficiency - symptoms because of spinal cord lesions

A
  1. ataxic gaits
  2. paresthesia
  3. impaired progression and vibration sense
  4. weakness
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9
Q

tabes dorsasis - spinal cord lesion?

A

degeneration (DEMYELINATION) of dorsal columns and roots

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10
Q

spinal trauma - treatment

A

glucocorticoids

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11
Q

spinal trauma - manifestation

A

acute onset of limb weakness and/or ensory disturbance below the level of the injury with the severity in proportion to the degree of injury.

  • Sphincter function impaired
  • loss of DTRs at the level of injury and hyperreflecia below
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12
Q

Brown-Sequard syndrome - manifestation

A
  1. ispilateral UMN signs below the level of lesion
  2. ipsilateral loss of tactile, proprioception, vibration below the level of lesion
  3. contralateral pain and temperature loss below the level of lesion
  4. Ipsilateral loss of all sensation AT LEVEL OF LESION
  5. ispilateral UMN sign at the level of lesion
  6. Horner syndrome (if lesion above T1)
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13
Q

syringomyelia ?

A

fluid filled, dilated central canal in pinal cord –> widening bubble or cavitation first damages neural fibers passing near the center of the spine (bytumore or trauma or congenital) –> loss of pain and Q bilaterally across the upper back and both arms (capelike distribution –> ALSO LOSS OF REFLEXES + MUSCLE ATROPHY IN THE SAME BILATERAL DISTRIBUTION

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14
Q

Tourrete Disorder - diagnostic tests / treatment

A
  • no specific diagnostic tests
  • fluphenazine, clonazepam, pimozide or other neuroleptic. Methylphenidate and ADHD treatment are intrinsic to Tourrete management
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15
Q

Huntington disease - chromosome of trinucleotide / trinucleotide repeat / age

A

ch 4
CAG
30-50

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16
Q

Huntington disease - symptoms

A
  1. choreiform movements (dyskinesia)
  2. aggression
  3. depression
  4. dementia
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17
Q

Huntington disease - movement disorder

A

starts with fidgetiness or restlessness progressing to dystonic posturing, rigidity and akinesia
- movement disorder may be troubling, but it is far worse to progress to no movement (rigidity)
(also athetosis and chorea)

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18
Q

Huntington disease - diagnostic test

A

specific genetic test (99% sensitive) –> CAG trinucleotide repeat sequences are found on genetic analysis –> symptom triad (movement/memory/mood) is confirmed with the test

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19
Q

Huntington disease - treatment

A

no treatment reveres HD

  • dyskenesia is treated with tetrabenazine, reseprine
  • psychosis is treated with Haloperidol, quatiapine
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20
Q

Huntington disease - MRI

A

Atrophy of caudate and putamen nuclei with hydrocephalus ex vacuo

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21
Q

Huntington disease - a common cause of death / is sometimes mistaken for

A
  • suicide

- substance abuse

22
Q

Restless Leg syndrome - presentation

A

patient reports an uncomfortable sensation in the leg that is creepy and crawly at night –> discomfort is worsened by caffeine and relieved by moving the legs.

23
Q

Restless Leg syndrome - treatment

A

dopamine agonists such as pramipexole

24
Q

Movement disorders - types

A
  1. athetosis 2. chorea 3, Dystonia 4. Essential tremor
  2. Hmiballismus 6. intention tremor 7. Myoclonus
  3. Resting tremor
25
Athetosis - presentation / characteristic lesion
slow, writhing (snake-like) movements, especially seen in fingers Huntington (basal ganglia)
26
Chorea - presentation / characteristic lesion
sudden, jerky purposeless movements | Huntington (basal ganglia)
27
dystonia - presentation and example
sustained involuntary muscle contraction ex: Writer's cramp blepharospam (sustained eyelid twitch)
28
hemiballismus - presentation / lesion
sudden, wild flailing of 1 arm +/- ispilateral leg | - contralateral subthalamic nucleus (eg. lacunar stroke)
29
intention tremor - presentation / lesion
slow, zigzag motion when pointing extending toward a target | - cerebellar dysfunction
30
Myoclonus - presentation / causes
sudden brief uncontrolled muscle contraction - hiccups are common - metabolic abnormalities such as liver or renal failure
31
Resting tremor - presentation / seen in
uncontrolled movement of distal appendages (most noticeable in hands) (pill rolling tremor) tremor alleviated by intentional movement - seen in parkinson
32
Essential tremor occurs
- at both rest and with intention - greatest in the hands but can affect the head as well - it may affect manual skills such as handwritting or the use of a computer keyboard
33
essential trempr
the best therapy is propranolol | - improved with alcohol
34
Parkinsonism - definition
loss of cells in the substatia nigra resulting in a decrease in dopamine --> significant movement disorder presenting with tremor, gait disturbance and rigidity
35
MCC of parkinsonism / other causes of parkinsonism
MCC of parkinsonism: idiopathic other: 1. encephalitis 2. drugs: a. metroclopramide b. reserpine c. antipsychotics
36
Parkinson disease - histology
1. Lewy bodies (composed of a-synuclein - intracellilar eosnophilic inclusions) 2. loss of dopaminergic neurons of substantia nigra pars compacta (de-pigmentation)
37
Parkinson disease - symptoms
MNEMONIC: TRAP 1. Tremor (pill-rolling tremor at rest) 2. Rigidity (cogwheel) --> slowing on passive flexion or extension 3. Akinesia (or bradykinesia) 4. Postural instability (orthostatic hypotenstion 5. Shuffling gait 6. FACIAL expression is limited (hypomimia and writing is small (micrographia)
38
Parkinson disease - age
50-60
39
all Parkinson drugs and mechanism of action (shortly)
1. Bromocriptine (dopamine agonist) 2. Pramipexole (dopamine agonist) 3. ropinirole (dopamine agonist) 4. amantadine (incr dopamine release and inh reuptake) 5. Levodopa (increases dopamine levels in CNS) 6. carbidopa (DOPA decarboxylase inhibitor) 7. entacapone(peripheral COMT inhibitor) 8. tolcapone (central and peripheral COMT inhibitor) 9. selegiline (MAO-B inhibitor) (and rasagilini) 10. benzotropine and trihexyphenidyl (antimuscarinic)
40
Parkinson disease - anticholinergic medications
benzotropine and trihexyphenidyl --> releive tremor and rigfitidy SE: dry mouth, worsening prostate hypertrophy, constipation
41
Parkinson disease - medication for patients above 60 with anticholinergic medications intolerance
amantadine
42
which medications are for mild parkinson disease
anticholinergic and amantadine (all the other are for severe - inability to care for themselves)
43
best initial therapy for severe parkinson
dopamine agonists: pramipexole, ropirinole
44
most effective medication for parkinson
Levodopa/carbidopa (ON/OFF episodes)
45
COMPT inhibitors - drugs / role
- tolcapone, entacapone - extend the duration of levodopa/carbidopa by bloccking the metabolism of dopamine - use when there are on/of, or when the response is inadequate
46
Parkinson treatment - electrical stimulation
highly effective for tremors and rigidity in some patients
47
MAO inhibitors - role / drugs / be careful
- resagiline, selegiline - adjunct to levodopa/carbidopa - block metabolism of dopamine avoid tyramine containing food --> hypertension
48
medications of Parkinson that slow progression of the disease
ONLY MAOi
49
antiprakinsonism medication complicated withpsychosis and confusion - next step
start antipsychotic with the fewest extrapyramidal effects (eg. clozapine) you cannot stop medications because lock in with severe bradykinesia
50
Shy-Drager syndrome
parkisnosnims predominantly with orthostasis
51
spasticity - definition, associated with
- painful, contracted muscles from damage of CNS | - associated with MS
52
spasticity - treatment
- no single treatment is universally effective | - baclofen, dantrolene and central acting α-agonists tizanadine