Neuro Flashcards
Alzheimers on imaging
mesial temporal lobe atrophy
anterior cerebral artery stroke
contralateral hemiparesis & sensory loss
Lower extremeties > upper extrem
Total anterior circulation infarct (TACI)
(middle and anterior cerebral)
1 unilat hempiparesis +/- hemisensory loss of face arms and legs
2 homonopious hemaonpia
3 higher cognative dysfxn ie dysphagia
anterior inferior cerebellar
lateral pontine
sudden onset vertigo & vom
ipsilateral facial paralysis and deafness
aphasia where is brocas and what time
presenation
suppilied by
expressive ie speech made then sent here
inferior frontal gyrus
normal comprehension
speech non fluent
repetition impaired
Superior dividion of MCA
aphasia where is wernickes
suplied by
presentation
speech made here then sent to brocas
superior temporal gyrus
inferior MCA
not normal comprehension
speech no sense, word substitution and nedograms
but fluent
‘word salad’
condustion aphasia where
and presentation
stroke in connection of arcuate fasiculus
speech fluent but poor
pt aware of errors
normal comprehension
global aphasia
where
presentation
large lesion affecting all 3
servere expressive and receptive aphasia
may still be able to communicate with gestures
true seizures may show compared to pseudoseizures
prolactin increase 10-20min after
parksinons path
loss of dopaminergic neruons in substantia nigra = loss of excitatory signal
less dopamine (d2) = less GABA (inhibitory) = increased movement
parkinsons tx
Motor sx impacting QOL = levodopa-carbidopa
Motor sx not yet impacting = Dop agonist ie ropinirole
MAO-B inhib ie selegiline
essential tremor presentation n tx
no tremor at rest
worsens with movement
propanolol
cerebellar lesion tremor
no tremor at rest
worsens w movement gets worse w intention ie closer u get
huntingtons ix
genetic testing - CAG repeats in HTT allele
CT/MRI
atrophy (caudate striatal frontal)
dilated lateral ventricles
huntingtons tx
supportive and sx tx
counselling n support for pt and family
psychiatric - SSRIs, ECT, antipsychotics,CBT
Chorea - benzos
Bradykinesia/rigidity - Dopamine agonists, levodopa
Spinal stenosis presentation
Bilateral
burning, lightening pain of thighs and bum
worse on upright - better when leaning forward or climbing stairs
(proximal pseudoclaudication that is positional!)
[peripheral cause would be distal legs too and not positional)
syringomyelia path and ix, sx and tx
associated with
pockets of CSF cysts in spinal cord
ix - MRI
sx - back pain (neck shoulders arms)
loss of pain and temp which progresses to motor sx ie weakness and wasting esp hands and arms
(bc spinothalamic )
Tx - Surgery
associated w chiari malformation (cerebeller tonsils protrude from foramen magnum
normal pressure hydrocephalus path presenation
ix
tx
normal ICP but hydrocephalus
Wet wobbly weird
(incontinence, ataxia, demetia)
ix
CT - hydrocephalus
LP - no raised ICP but improvement of Sx after
tx surgical shunt
picks disease
FTD dementia
lewy body pathway n presentation
Lewy bodies in substantia nigra
fluctuating changes in cognition - cycles get progressively shorter
w lucid period - can be v distressing for pt bc insight
acute delirium and hallucinations
alzheimers tx
cholinesterase inhib
donezepil n rivastigmine
severe = memantine
CJ disease (mad cow)
prions accumulation
young rapid dementia myoclonus
Reversible causes of dementia
b12 def
hypothyroid
electrolyte abnormality (CKD)
syphilis
Normal pressure hydrocephalus
anaemia
Anterior spinal artery occlusion
bilateral spastic paresis
loss of pain and temp
when does cushings reflex happen why
what is it
happens in increased ICP to maintain peripheral perfusion
opposite of hypovol shock vitals ie
increase BP (HTN)
decrease HR
wide pulse pressure
Bitemporal hemanopia if upper quad worse then lower
pituatry tumor
bitemporal hemanopia
lower quad worse than upper
craniopheningoma
pontine haemorrahe cause and presentation
life threatening emergency
chronic HTN complication
reduced GCS
quadraplegia
miosis
absent horizontal eye movements
extradural haemorhage
middle meningeal artery
MCA stroke presentation
contralateral paralysis and sensory loss of face and upper limbs
aphasia if infarct in dominant hemisphere
bells palsy
no foreheard sparing (bc LMN)
loss of taste anterior 2/3 tongue
wilsons neuro sx
copper deposition in cerebellum = dysarthria and wide based gait
in basal ganglia = tremor and rigidity (parkinsonism)
also psych sx ie anxiety depression bipolar
wilsons diagnostic test
24hr urine collection
L5 root lesion
reduced ankle eversion and inversion and dorsiflexion
sensory loss over big toe
pundendal nerve block what nerve fibres and palpate where
fibres S2,S3,S4
palpate ischial spine transvaginaly
GCS
eyes
Eyes open spontaneously – 4
Eyes open to speech – 3
Eyes open to pain – 2
Eyes do not open – 1
GCS
verbal
Orientated – 5
Confused – 4
Inappropriate words – 3
Inappropriate sounds – 2
No verbal response – 1
GCS
motor
Obeys commands – 6
Localises pain – 5
Withdraws from pain – 4
Abnormal flexion – 3
Abnormal extension – 2
No response – 1
Charcot marie tooth disease (CMT)
hereditary peripheral neuropathy
distal weakness, such as foot drop and pes cavus (high foot arch)
distal atrophy
loss of senstation maybe tingling and numbess
stroke no driving for how long
4 weeks
duchenne muscular dystrophy tx
steroids
brown sequard
hemisection of cord
ipsilateral loss of vibration and proprioception and hemiplegia
contralateral pain and temp
pinealoma
slowgrowing tumor of pineal gland
may press on midbrain cerebral aqueduct = non communicating hydrocephlaus
if compress edinger westphal nuclei = mydriasis (pupil dilation)
had two epsiodes of seizure both resolved but now having another seizure
IV phenytoin
LP spinal level and to which space
L3/L4 (cord ends at L1/L2)
into subarachnoid space
spontanous intracranial hypotension
postural headache worse when standing/sitting - relieved by laying down
Extrathecal leakage of CSF
diagnosed CT myelogram
Tx epidural blood patch
common cause = LP
loss of vision right upper quad of both eyes
left inferior optic radiation
bacterial meningitis CSF
CSF pressure raised
protein raised
glucose low
polymorphs
MMSE score
out of 30
<26 abnormal
20-26 mind dementia
10-20 moderate dementia
degenerative cervical myelopathy (DCM)
what is it
progressive degen of spinal cord in cervical
- associated w age related changes in spine and caused by wear and tear over time
leads to compression and damage of spinal cord
Age related changes
- herniated discs between vertebae (bulge/herniate -= compress cord)
- Osteophytes (abnormal bony outgrowths= same)
- Ligament thickening (ligs in spine thicken = same)
ix MRI
tx decompressive surgery
Homonymous quadrantopia
PITS
parietal = inferior
Temporal = superior
webers syndrome
Stroke of Posterior cerebral artery
ipsilateral oculomotor palsy (bc CN3 runs close to PCA in midbrain)
contralateral hemiparesis