Neuro Flashcards

1
Q

TIA

Path
RFs
Symps
DDx
Ix
Mx
A

transient ischaemia (emboli/thrombosis) resolved in 24hrs

Same as stroke

-Transient global amnesia
90% - anterior circulation (one-sided carotid territory)
-hemiparesis, amaurosis fugax, dysphasia, hemisensory disturbance
10% - posterior (vertebro-basilar)
-LOC, bilateral motor+sensory probs

Stroke, hypoglycaemia, focal epilepsy
Todd’s paralysis - focal weakness one sided after seizure

Bloods
ECG - AF/myocardial ischaemia
Carotid doppler
Echo

ABCD2 score - assess stroke risk (high risk >4 = specialist assessment in24hrs, low risk 1week)
-AF, >1 TIA in week, TIA on anticoag = high risk
Control CV risk - weight loss, diet, smoking etc…
No driving 4 weeks

2 weeks 300mg Aspirin
Long term anticoag - clopidogrel
Statin
Carotid endarterectomy - 70% stenosis

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2
Q

Stroke territory types / arteries affected / symps?

A

Anterior Circulation (MCA/ACA)

  • Unilateral weakness (+/- sensory deficit) - face, arm, leg
  • Homonymous hemianopia
  • High cerebral dysfunction (dysphasia, visuospatial disorder)

Partial anterior circ - 2outof3 symps ^^

Posterior circulation (POCS) - ONE OF:

  • Cerebellar / brainstem syndromes
  • LOC
  • Isolated homonymous hemianopia

Lacunar syndrome (subcortical/midbrain/internal capsule)

  • Unilateral weakness (+/-sensory loss) - face/arm/leg
  • Ataxic hemiparesis (cerebellar + motor symps)
  • Pure sensory loss
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3
Q

Stroke Mx?

A

ABCDE - hydration, O2, nil by mouth
URGENT CT HEAD - before tx = could be haemorrhagic

if onset time known:
Alteplase (WITHIN 4.5HOURS) –> 24 hours –> 75mg clopidogrel

if time not know:
300mg Aspirin –> 2weeks –> Clopidogrel life long

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4
Q

SAH

Path
RFs
Symps
Ix
Mx
Comps
A

berry aneurysm

HTN, aneurysm, FH, predisposition to aneurysms (PCOS, Ehler-danlos, coarctation)

Thunderclap headache, vomiting
Neck stiffness -kernig's sign 
Altered consciousness - collapse, seizure, drowzy, coma 
Papilloedema 
CNS def - cranial nerves, hemiplegia 

CT - Star-shaped lesion
LP - IF NO ^ICP (done if -ve CT)
-blood –> few hours –> yellow (xanchromic - due to bilirubin from Hb breakdown)

Nipodipine - stop vasospasm + ischaemia
Maintain cerebral perfusion - fluids, DEXAMETHOSE (lower cerebral oedema)
Surgery - clip/coil aneurysm

Comps
hyponatraemia - SIADH
hydrocephalus

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5
Q

Subdural Haematoma

Path
RFs
Symps - acute/chronic
DDx
Ix - SHAPE??
Mx
Comps
A

Rupture of bridging veins = deceleration injury
^ICP - shifting of midline

Trauma, ^age - bridging veins more vulnerable, Alcoholism, coagulation

Interval between injury–>symps = days-months
ACUTE:
-^ICP - headache, nausea, vom, HTN
-Focal neuro
-altered consciousness - seizures, confused…
CHRONIC:
-cognitive decline, personality change, headache
-ELDERLY –> symptoms evelove SLOW –> personality+decreased GCS…

EDH, SAH, ICH (contusion), Stroke, Dementia, encephalitis

CT - CRESCENT SHAPE - crosses suture lines
–>N.B. as clot ages density changes
Bloods

ABCDE- prioritise CT
Surgery - craniotomy
Manniotol - if ^ICP

Comps:
Death - due to herniation
^ICP, cerebral oedema

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6
Q

Extra dural haematoma

Path
RFs
Symps - Main COMP - BAD!!!
DDx
Ix - SHAPE!!!!
Mx
A

Laceration middle meningeal artery - trauma to temple
Rapid (mins-hours) blood accumulation between bone + dura

Young adults, temporal/parietal bone fracture, RUGBY PLAYERS!!

Brief post-trauma LOC –> LUCID PERIOD (hours-days) –> altered consciousness
^ICP - Headache, nausea, vomiting, seizures, confusion
Neuro def - seizures, contralateral hemiparesis

IMPORTANT - may be RAPID ^ICP
–> ipsilateral pupil dilatation, signs of brainstem compression, DEATH!!

SDH, SAH, ICH (contusion), encephalitis

CT - BICONVEX
X-ray - skull fracture

ABCDE
Mannitol
Surgery - craniotomy

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7
Q

Tension Headache

Path - episodic vs chronic
RFs
Symps 
DDx
Ix 
Mx
A

Episodic <15days/month
Chronic >15days/month for 3 months

Triggers - stress, anxiety, fumes, concentrated visual effort, noise

‘Tight band’ - bilateral ,non-pulsatile, chronic daily
[NOT - aura, nausea, vom, sensitivity to movement]

Migraine, cluster, drug-induced, GCA

CLINICAL
Headache diaries useful

Analgesia - NSAIDs, aspirin, paracetamol - NOT OPIOIDS
Stress relief - massage, acupuncture
lifestyle - reassurance, avoid triggers, diet, exercise
(maybe amytryptilline / other anti-depressants)

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8
Q

Migraine

Path
RFs
Symps 
DDx
Ix 
Mx
A

Throbbing headache preceded by aura

F>M, strong genetics
Triggers - caffeine, chocolate, cheese, alcohol, menstruation, oral contraceptives, exercise , anxiety

+/- Aura - 5-60mins (headache following within 1hour)

  • Visual (jagged lines, flashing, hemianopia)
  • Sensory (paraesthesia, numbness)
  • motor, vestibular
Lasts 4-72hours - mod-severe
THROBBING, PULSATILE, UNILATERAL, AGRRAVATED BY MOVEMENT
Nausea/vomiting 
Photophobia 
Phonophobia - FEAR of loud sounds 

tension headache, cluster headache, GCA

CLINICAL DIAGNOSIS - test to rule out co-morbs
CRP, ESR
Imaging / LP indications - worse/severe headache, changing symptoms, posterior headaches, abnormal neuro

Sumatriptan + NSAID/paracetamol + antiemetic
Prophylaxis (2+ per moth / acute mx >2/week)
-Propanolol / topiramate

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9
Q

Cluster Headache

Path
RFs
Symps 
DDx
Ix 
Mx
A

Unilateral, rapid onset, around one eye
In ‘clusters’ of 1-2x/day –> over 5-12weeks –> pain free for months-years
**can be chronic

Smoking, M>F 5:1

Rapid, excruciating pain around one eye
 - rises to crescendo in minutes 
 - lasts 15-160mins
 - often wakes from sleep 
Watery/bloodshot eye - lacrimation, lid swelling, facial flushing. miosis/ptosis 
\+/-vomiting 

Migraine

CLINICAL

Abortive: O2, SUMATRIPTAN 
Preventative: 
 - Verapamil - 1st line 
 - Avoid alcohol - during headaches 
 - Prednisolone (may help)
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10
Q

Trigeminal neuralgia

Path
RFs - main one? 
Symps - triggers?
DDx
Ix 
Mx
A

Paroxysms of intense, debilitating pain - in CN V distribution (mainly maxillary+mandibular branches)
N.B. CN V = motor + sensory
Compression of trigeminal nerve - from blood vessels/local pathology = demyelination + excitation –> erratic pain signalling

F>M, 50 peak age
HTN - MAIN RF

Sudden, unilateral, knife-like electric shock pain
- starts in mandibular + spreads up
- seconds-mins –> many through day, rarely in sleep
Atypical –> burning sensation
TRIGGERS - shaving, eating, talking, cold wind exposure, dental prostheses, vibration –> i.e. using nerve

MS, GCA - RULE IT OUT!!

MRI - exclude secondary causes /other path

typical analgesia + opioids DO NOT WORK
Carbemazepine (others: Gabapentin, lamotrigene)
Surgical - neurovascular decompression
Radiation - stereotactic radiosurgery

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11
Q

GCA aka Temporal arteritis

Path
RFs
Symps 
DDx
Ix 
Mx
Additional diagnosis?
A

Inflammatory granulomatous vasculitis of large cerebral arteries
EXCLUDE IN ALL >50YEAR OLDS WITH NEW HEADACHE THAT HAS LASTED FEW WEEKS

Male, >50years

Takyasu’s - if <50 + esp. Japanese

TEMPORAL PULSATING HEADACHE
SCALP TENDERNESS
JAW CLAUDICATION
AMAUROSIS FUGAX
Tender, thick, pulseless temporal artery
morning stiffness, fatigue, breathless, fever
RISK - ANTERIOR ISCHAEMIC OPTIC NEURITIS

CRP/ESR^ - vasculitis
FBC - normochromic anaemia
Teporal artery biopsy
Doppler USS

Prednisolone
PPIs, bisphosphonates

PMR = presents in 50%!!! - morning stiffness!!

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12
Q

Encephalitis

Path
RFs - bugs?
Symps 
DDx
Ix 
Mx
Comps
A

Infection + inflammation of brain PARENCHYMA
-Mainly affecting frontal+temporal lobes

VIRAL - HSV1+2 most common (CMV, EBV, varicella)
non-viral - post meningitis

Extremes of age, immunocompromised

viral infection - headache, fever, fatigue, nausea
Progression:
- DECREASED CONSCIOUSNESS / CONFUSION!!!
- focal neuro def
- seizures
- coma
(may have signs of meningitis)

Meningitis, stroke, brain tumour, space occup. lesion

LP + CSF studies (cultures + PCR)
- +proteins, lecuocytes +/- glucose
FBC+blood film - lecuocytosis
Bloods
Viral PCR + Blood cultures (and others..throat, stool)
CT/MRI - rule out space occupying lesions + identify ^ICP (LP=CI!!!!!)
EEG - diffuse abnormal slow wave changes

Acyclovir
meningitis? - IV BenPen
Supportive +/- anti-seizure meds

Permanent brain damage - if Mx delayed

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13
Q

Meningitis. Define meningococcal septicaemia

Path
RFs - bugs? spread?
Symps 
DDx
Ix - what is seen?? - for each of bacteria/virus
Mx - when do you start Abx? 
Comps
A

Inflammation of meninges
Meningococcal septicaemia = when it invades the blood

N. meningitides - droplet spread 
S. pneumoniae, H.influenza (less common)
Preg - listeria monocytogenes 
Neonates - GBS, E.coli 
immunosuppressed - TB, CMV
Fever 
**Headache - worst ever 
**Meningism - Neck stiffness, Photophobia - Kernig's + Brudzinski's 
NON BLANCHING RASH
sezures 
\+/-altered mental state (cerebral oedema)

SAH (headache more sudden)
Encephalitis (altered mental state = dominant symp)

FBC, Blood culture, Swabs, PCR
LP - microscopy, culture, glucose, PCR (ONLY IF NO ^ICP)
- Bacteria: cloudy, ^protein, low glucose, neutrophils
- Virus: clear, ^protein, normal/low glucose, lymphocytes

NOTIFIABLE DISEASE
**Start before tests!! 
IV Cefotaxime 
community - IM BenPen 
Dexamethasone - cerebral oedema 
Prophylaxis - ciprofloxacin / rifampicin 

hearing loss, seizures, dev problems

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14
Q

Guillain-Barre syndrome

Path
RFs - bugs?
Symps 
DDx
Ix 
Mx
A

Acute inflammatory, demyelinating, ascending polyneuropathy - following URTI / GI infection
infection –> antibodies/inflammation –> demyelination

40% - no obvious infectious cause
*Campylobacter jejuni, *CMV, Mycoplasma, zoster, EBV

1-3 weeks post infection:
symmetrical, ascending muscle weakness +/- numbness
GLOVE + STOCKING - distal muscles + progresses
Loss of reflexes, neuropathic pain
Autonomic dysfunction (tachycardia, sweating, arrhythmias)
20% - resp muscles involved - ITU!!

acute paralysis: stroke, TIA, encephalitis, cord compression
peripheral: vasculitis

Nerve conduction studies - slow conduction
LP - ^protein, normal WCC
Spirometry - resp muscle involvement? ITU?

SELF-LIMITING
IV immunoglobulin (decreases severity + duration of paralysis
Monitor ventilation

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15
Q

Epilepsy

Path
RFs 
Symps 
DDx
Ix 
Mx
Who must be informed?
A

Recurrent spontaneous, intermittent, abnormal, electrical activity - in form of seizures
Seizure = clinical feature of desynchronus neuronal discharge

40%-Primary generalised - bilateral symmetrical synchronus –> no focal abnormality
57%-Partial - One hemisphere (focal/structural abnormality until proven otherwise)

Mostly idiopathic
Cerebrovascular disease, tumour, CNS infection, Trauma

Symps - SEE TYPES OF SEIZURE CARD + LOBE CARD
POST - ICTAL (esp tonic-clonic)
- confusion/drowzy/coma - up to hours

SYNCOPE!!
arrhythmia, TIA, Migraine, hypoglycaemia, panic attack, non-epileptic seizure

CLINICAL - 2 unprovoked seizures, 24hours apart
EEG - only supports diagnosis
Bloods - DEFG!
MRI>CT - ?structural

Primary generalised - Valproate / Lamotrigene
Absence - Valproate / ethosuxamide
Partial - Carbemazepine / Lamotrigene

MUST INFORM DVLA:

  • FORMAL EPILEPSY DX = 1year w/o seizure
  • 1 seizure = wait 6months
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16
Q

Types of seizures:

1) Primary
2) Partial - simple, complex?

A

PRIMARY
Generalised tonic clonic - stiff then jerking. BITE TONGUE
Clonic seizures - repeated myoclonic 2-3 per second
Tonic seizures - sudden increased tone - characteristic guttural cry/grunt
Absence
Myoclonic seizures
Atonic seizure –> sudden loos of tone

PARTIAL - i.e. focal seizures
Simple 
 - 90secs
 - No LOC, sudden jerking, sensory phenomena, aware of surroundings  
 - NO post-ictal 

Complex

  • 1-2mins
  • automatisms (lip-smacking, chewing), AURA, unaware of environment, LOC
  • Post-ictal symps

Partial w/ secondary generalisation - partial –> generalised

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17
Q

Epilepsy symps for each lobe - i.e. partial seizures?

A

Temporal:
- Aura - deja-vu, audito hallucinations, funny smells, fear

Frontal
- Motor features. Jacksonian march

Parietal
- Sensory disturbance - tingling/numbness

Occipital
- visual phenomena

18
Q

SUDEP? What?

A

Sudden unexpected death in epilepsy

-non-drowning death

19
Q

DEFINE + Management of prolonged seizure / status epilepticus!!!

A

Seizure lasting >30mins / recurrent seizures w/o full recovery between

ABCDE --> DEFG!!
oxygen
buccal midaz / rectal diaz / IV loraz
repeat IV loraz
IV Phenytoin / Valproate 
Anaesthetist
20
Q

Parkinson’s

Path
RFs 
Symps - TRIAD???
DDx
Ix 
Mx - Problem with 1st line?
A

LOSS OF DOPAMINE AND MELANIN IN STRIATUM
degeneration of dopaminergic neurons in substantia nigra
Lewy bodies develop - eosinophillic inclusions of ubiquitin + alpha-synuclein

peak onset 55-65yrs - ^prevalence with age

insidious - commonly impaired dexterity + unilateral foot drop 
TRIAD - RESTING TREMOR, BRADYKINESIA, RIGIDITY 
 - tremor = pill-rolling 
Others:
 - Difficulty with fine movements
 - Cogwheeling 
 - Parkinsonian gait 
 - postural instability - falls 
 - Micrographia 
 - brisk reflexes 
 - monotonous scattato speech 
 - depression, anosmia, visual hallucinations, constipation, urinary incontinence/freq. 

Lewy Body dementia, Parkinsons plus, drug-induced (EPSE), Wilson’s

CLINICAL DIAGNOSIS
response to Levodopa - to confirm
MRI - later show substantia nigra atrophy

MDT - progressive + incurable
GOLD - LEVODOPA + CARBIDOPA (decarboxylase inhibitor –> prevents L-DOPA peripheral conversion)
- N.B. L-DOPA ONLY SYMPTOM RELIEF

Other treatments - due to L-DOPA limitations (don’t start until absolutely necessary)

  • Dopmaine agonists - ropinirole
  • MOABs - rasagiline
  • COMT inhibitors - tolcapone
21
Q

Limitations of L-DOPA. Reason why it’s not started until absolutely necessary

other treatments offered first?

A

Reduced efficacy over time - even with ^dose
Induced dyskinesia
on-off effect –> fluctuations in motor performance

  • Dopmaine agonists - ropinirole
  • MOABs - rasagiline
  • COMT inhibitors - tolcapone
22
Q

Parkinson plus syndromes?? 4 of them!

A

Progressive supranuclear palsy

  • Postural instability - falls
  • vertical gaze palsy

Multiple system atrophy

  • autonomic features - postural hypotension, urinary dysfuction)
  • cerebellar signs - DANISH

Corticobasal Degeneration

Lewy Body dementia - if motor symptoms + dementia TOGETHER
- if dementia >1year after motor = feature of parkinsons!

23
Q

HUNTINGTON’S

Path
RFs 
Symps 
DDx
Ix 
Mx
A
AUTOSOMAL DOMINANT 
CAG repeats  
Decreased GABA + ACh synthesis 
(normal dopamine)
Progressive cerebral atrophy in caudate nucleus and putamen - in basal ganglia 

30-50years = onset

Chorea - jerky, repetitive, explosive, figidity movements
Personality change (e.g. irritability, apathy, depression) + intellectual impairment (dementia)
Dystonia
Saccadic eye movements

Syndenham’s chorea, Wilson’s Disease

CLINICAL
CT/MRI - caudate nucleus atrophy
Genetic testing - CAG repeats

No Mx to prevent progression 
Counselling 
Chorea - tetrabenazine, benzos, valproic acid 
Antidepressants 
Antipsychotics
24
Q

MOTOR NEURONE DISEASE

Path
RFs 
Symps - 4 TYPES!! What is spared??
DDx
Ix 
Mx
A

Progressive degenration of motor nerves in:

  • Spinal cord - anterior horn
  • CN motor nuclei
  • Brain cortex

Genetic
Mainly sporadic - unknown trigger

Mixtures of UMN/LMN signs depending: 
Amyotrophic Laterelising Sclerosis (ALS):
 - UMN + LMN 
 - Frontotemproal dementia link 
 - regardless what body part first affected = spreads to other parts of body
Primary Lateralising Sclerosis (PLS)
 - UMN 
Progressive muscular atrophy (PMS)
 - LMN
Progressive Bulbar palsy (PBP)
 - UMN + LMN of lower CN 
 - early bulbar symps - dysphagia + dysarthria 

3 PATTERN OF ONSET:

  • Limb
  • Bulbar (20%)
  • Resp onset (least common)

SPARED:

  • RECTAL/BLADDER SPHINCTERS
  • OCULOMOTOR MUSCLES

CLINICAL
EMG/nerve conduction
Genetics - research only

RILUZOLE!!! - not a cure extends life by 3months 
MDT
Symptomatic - e.g.:
 - baclofen - spasms 
 - PEG tube for feeding 
 - Non-invasive ventilation
25
Q

UMN + LMN SIGNS?

A
UMN: - FOREHEAD SPARING!!
Weakness
Hypertonia 
\+ve Babinski's - upward going plantars 
Clonus 
Brisk reflexes 
LMN:
Weakness 
Absent reflexes 
Hypotonia 
Wasting 
Fasiculations
26
Q

Multiple Sclerosis

Path
RFs 
Symps - subtypes?
Ix 
Mx 
How do patients often die?
A

Chronic inflammation (demyelination) of CNS - with progressive disability
T-cell mediated: activate B-cells - antibodies attack
Repeat demyelination - axonal loss + incomplete recovery between attacks

Causes not known - ?infection (EBV, MMR) - REMEMBER CMV = GUILLIAN BARRE

  • Smoking
  • Vit D deficiency

White, F>M

Relapsing-remitting (80%) - come+go
Secondary progressive - relasing-remitting first then symptoms progressive
Primary progressive - symptoms gradually develop from start - no remit

Unilateral OPTIC neuritis - DIPLOPIA, pain on movement, reduced central vision
Lhermitte’s sign - neck flexion = electric shock
UHTOFF’s - worse in hot water/weather
Charcot’s neuro triad: Nystagmus, Intention tremor, Dysarthria
sensory disturbance - tingling, numbness
UMN signs
Bladder/sexual dysfunction

> 2 CNS LESIONS DISSEMINATED IN TIME + SPACE
Exclude differentials - Bloods, inflam markers, HIV, glucose
Neuro:
- Nerve conduction - slow
- MRI
- LP + CSF - ^protein. OLIGOCLONAL BANDS OF INCREASED IMMUNOGLOBULIN CONCENTRATION

Relapse - IV methylpred
DMARD - reduce rate + severity of relapses:
- Alemtuzumab / Natalizumab / Dimethyl fumarate
Palliation:
- Baclofen / benzos (spasticity)
- Catheter - urinary stuff

Aspiration pneumonia often kills patients

27
Q

MYASTHENIA GRAVIS

Path
RFs 
Symps
DDx 
Ix 
Mx
A

FATIGUEABILITY + WEAKNESS
AI disorder affecting neuromuscular junction
- ABs against ACh receptors – AChR IgG immune complexes deposited at post-synapse

F>M
AI association: SLE, RA, Thyroid

WEAKNESS AND FATIGUEABILITY
- proximal limb muscles, speech, facial expression, extra ocular
- resp muscles = acute resp failure - ventilation
NO PAIN, SENSORY CHANGE, WASTING
NORMAL TONE + REFLEXES

DDx - Lambert Eaton myasthenic syndrome (REMEMBER SMALL CELL paraneoplastic feature)

Serum ABs - Anti-AChR + anti-MuSK
Thymus CT - hyperplasia in 70%
Tensilon test
Neurophysiology - FATIGUEABILITY - decreased eoked muscle action potentials with REPEAT nerve stimulation

N.B. exacerbations are unpredictable + sometimes unprovoked
Symptoms - NEOSTIGMINE - AChE inhibitor
Immunosuppresson - Pred
Thymectomy

28
Q

Primary and Secondary Brain Tumours

Path 
RFs 
Symps
Ix 
Mx
A

TYPES = see next SLIDE

Most common 50-70years

^ICP headache - worse in morning/lying down
- unilateral ptosis, papilloedema, pupil changes
Seizures
N+V
Neuro focal symps - HIGH GRADE
Personality change, cognitive/behavioural symps, confusion
CONING –> resp depression, bradycardia, death
- herniation of cerebellar tonsils through foramen magnum

CT / MRI

Surgery = resection
Radiotherapy
Supportive

29
Q

Types of brain cancer. High grade, low grade, mets?

How are brain tumours graded?

A

High Grade:

  • Gliomas (astrocytoma, oligodendroma) = most common primary
  • primary cerebral lymphoma, medullobastoma

Low grade:
- Meningioma (benign), acoustic neuroma (CN VIII sheath), Neurofibroma, Pituitary tumour, pineal tumour

Mets: Lung, breast, prostate, colorectal, melanoma, kidney

Grading (I-IV):

  • I+II = benign
  • III + IV = malignant
30
Q

Spinal Cord Compression Vs root compression - name? signs?

Note about disc + root levels?

A
Cord = myelopathy - UMN 
Root = radiculopathy - LMN 

Root comes out ABOVE LEVEL –> disc herniation will affect number BELOW!!
- L4/L5 herniation = L5 root compression!

31
Q

Spinal cord compression

RFs
Symps
Ix
Mx

A

Disc herniation / prolapse

DEPENDS ON LEVEL
(S1 compression / sciatica)
- sensory loss - back of thigh/leg, lateral little toe
- Foot drop - plantar flexion weakness
(L5 compression)
- Sensory loss - Lateral thigh/leg, medial big toe
- Dorsiflexion weakness

MRI - GOLD STANDARD
CXR - malignancy?
Bloods

Surgery

32
Q

Cauda Equina - EMERGENCY!!

Path 
RFs 
Symps
Ix 
Mx
A

Nerve root compression L4/L5 // L5/S1 - generally S1-S5 root compression

Disc herniation, trauma, tumour/mets, congenital (spina bifida)

Bilateral/Unilateral leg pain 
Varying leg weakness 
Poor anal tone 
Saddle anaesthesia 
Urinary/bowel dysfunction - loss of control - retention + bowel incontinence 
Erectile dysfunction 

MRI

Neurosurgery ASAP - risk of irreversible paralysis/sensory loss/incontinence

33
Q

Define different types of peripheral neuropathies:

  • Demyelination
  • Axonal degenration
  • Compression
  • Infarction
  • Infiltration
  • Wallerian degeration
  • Carpal Tunnel
A
  1. Schwann cell damage. Marked slow conduction - Guillian Barre!
  2. leads to dying nerve firing back - initially conduction okay as fibres remaining sort it. E.g. toxic neuropathies
  3. Focal demyelination at points of compression
  4. Microinfarction of vasa nervorum (blood supply to peripheral nerves) - in diabetes. Wallerian degen = distal to infarct
  5. Inflam cells - neoplasms, leprosy…wtf
  6. When nerve fibre cut/crushed/infarcted - distal part of axon separated
  7. Median nerve entrapment at wrist
34
Q

Peripheral neuropathy symps / signs??

A

SENSORY
- changes in - pain, temperature, vibration, crude touch, proprioception

AUTONOMIC - changes in:

  • sweating
  • temp reg
  • CV - orthostatic hypotension, arrhythmias, syncope
  • Resp - reflex to hypoxia in DM change
  • GI - constipation/diarrhoea, dry mouth, incontinence
  • Sexual - impotence, ejaculatory failure
  • Feet - trophic changes, pale cold
35
Q

Carpal tunnel syndrome

Path
Symps
Ix
Mx

A

Median nerve entrapment at wrist

TINGLING - hand/forearm - poorly localised (not confined to anatomical sensory areas)
Weakness + wasting = LATE

Phalen’s test + Tinel’s test

Wrist splint @ night
Localised steroid injection
SURGICAL DECOMPRESSION - definitive

36
Q

Brachial plexus injuries? Erbs vs Klumpkes?

A

Erb-Duchenne paralysis
damage to C5,6 roots
winged scapula

Klumpke’s paralysis
damage to T1
loss of intrinsic hand muscles
due to traction

37
Q

Causes of Cerebellar injury

A
P - Posterior fossa tumour
A - Alcohol
S - Multiple sclerosis
T - Trauma
R - Rare causes
I - Inherited (e.g. Friedreich's ataxia)
E - Epilepsy treatments
S - Stroke
38
Q

Bell’s Palsy?

Path
Symps
Mx

A

FACIAL NERVE PARALYSIS - acute, unilateral

idiopathic

LMN! - forehead affected
Auricular pain, altered taste, DRY EYES, hyperacusis

PREDNISOLONE
Eye care - artificial tears, eye lubricants

39
Q
Reflexes ? 
Ankle
Knee
Biceps
Triceps
A

Ankle S1-S2
Knee L3-L4
Biceps C5-C6
Triceps C7-C8

40
Q

Epileptic seizure vs Pseudo seizure

Other features of pseudo-seizure (unique)

A

RAISED PROLACTIN - epileptic seizure

Sx of pseudo:

  • Hip thrusting
  • crying after
  • gradual onset