Neuro Flashcards

1
Q

General inspection of Parkinson’s disease

A

Hypomimia
Resting tremor - exacerbated by counting backwards
Stooped posture

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2
Q

Eye exam in parkinson’s disease

A

Nystagmus –> MSA?

Vertical gaze palsy –> PSP?

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3
Q

Gait in parkinson’s disease

A

Stooped
Shuffling
ABSENT ARM SWING
Slow initiation

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4
Q

Extras to an examination of PD patient

A
  • Assess for micrographia
  • Assess gait
  • BP lying + standing
  • MMSE
  • Drug chart
  • Abdominal examination
  • Abdo exam (Wilson’s disease = liver failure)
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5
Q

Causes of parkinsonism

A
  • Idiopathic
  • Parkinson + (MSA, PSP, Lewy body)
  • Multiple SNigra infarcts
  • Wilson’s disease
  • Antipsychotics
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6
Q

What parts of the Hx may point you towards a cause for parkinsonism?

A
  • Lewy body: visual hallucinations, memory problems
  • Infarcts in SN: sudden onset
  • MSA: postural hypotension, bladder/bowel problems
  • Antipsychotics: drug Hx
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7
Q

Ix in ?PD?

A

It’s a clinical dx!

but must do CT/MRI to exclude a vascular cause

  • DaTscan (iodine isotope injection which binds to DAergic neutrons in SNigra)
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8
Q

Medical Tx of Parkinsons

A

L-DOPA + DDCinhibitors

  • DA agonists (ropinirole)
  • MAO-B inhibitors (Selegiline)
  • COMT inhibitors (entacapone)
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9
Q

Unwanted side effects of L-DOPA?

A
  • Dyskinesias (occur in peak therapeutic effect)
  • On-off effect
  • Psychosis
  • Nausea/GI upset
  • Hypotension
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10
Q

Features of parkinsonism

A
  • Bradykinesia
  • Rigidity
    • Tremor
      Gait: slow to start, festinating, absent arm swing, shuffling
  • Hypomimia
  • Micrographia
  • SLEEP disorder
  • Depression
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11
Q

Sleep disorder in PD patients

A
  • Insomnia + frequent waking
  • Restless legs + early morning dystonia
  • Nocturia (from auto- dysfunction)
  • Violent enactment of dreams
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12
Q

Features of PSP?

A

Postural instability –> falls
Vertical gaze palsy
Speech + swallow problems (pseudo bulbar palsy)

Tremor is unusual

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13
Q

Features of Lewy body dementia

A

Parkinsonism precede memory loss

Visual hallucinations!

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14
Q

Ddx for tremor

A

Intention tremor = cerebellar

Resting tremor = parkinsonism

Postural (i.e. worse w arms outstretched)=

  • Thyroid
  • EtOH withdrawal
  • SABA/LABA use
  • Anxiety
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15
Q

Features of multi system atrophy

A

Autonomic dysfunction: postural hypo, bladder/bowel dysfunction

Cerebellar syndrome!!!
- nystagmus

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16
Q

how many cervical nerves and cervical vertebrae

A

Cervical nerves: C1-8
Cervical vertebrae: C1-7

All cervical nerves arise from ABOVE their corresponding vertebrae BUT C8 nerve arises from between C7 and T1 vertebrae

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17
Q

symmetrical + distal LMN signs = where is the lesion?

What are the differential

A

Peripheral motor polyneuropathy

  • Charcot Marie Tooth
  • Paraneoplastic
  • Guillain-Barré syndrome
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18
Q

Findings on examination in Charcot Marie Tooth?

A
  • Champagne bottle legs
  • Highs stepping gait w foot drop
  • High- arched foot
  • Sensory loss in stocking distribution
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19
Q

Investigations in Charcot Marie Tooth

A

Nerve conduction studies

Genetic testing

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20
Q

Mx of Charcot Marie tooth

A

Supportive
MDT: GP, physio, neurologist, specialist nurse OT
- foot care + special shoe choice
- ankle braces

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21
Q

Define GBS

A

autoimmune demyelinating polyneuropathy

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22
Q

Features of GBS

A

preceding infection (campylobacter)

  • ascending hypotonia + weakness
  • paraesthesia
  • breathing + swallowing probs
  • Autonomic probs: labile BP, urinary retention
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23
Q

Pathophysiology of GBS

A

cross-reactivity of antibodies to infection –> attacks gangliosides

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24
Q

Ix for diagnosis of GBS

A
  • Look for infection eg stool culture
  • Anti-ganglioside antibodies
  • Nerve conduction studies (low conduction velocity due to demyelination)
  • LP: high CSF protein levels!
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25
Mx of GBS
Supportive: AIRWAY: ITU if FVC<1.5L ANALGESIA AUTONOMIC: catheter +/- inotropes Definitive: IVIG, plasma exchange Physio
26
Ddx for bilateral + symmetrical proximal muscle weakness
Proximal myopathy Endocrine: DM, hyperthyroidism, cushings, acromegaly EtOH, statins, steroids Paraneoplastic Inherited: MD Inflammatory: Dermato/polymyositis
27
Ddx for Hand wasting
Muscle atrophy - think LMN AHC: MND, old polio, Charcot Marie Tooth Nerve root (C8T1): Spondylosis Plexus: cervical rib compression Neuropathy: Charcot, DM Muscle: RA (disuse), myotonic dystrophy
28
Ix for proximal myopathy
``` Glucose/HbA1c TSH 9am cortisol LFTs - alcohol CK (statins) Anti-jo1 CXR EMG Genetic analysis ```
29
CN7 palsy - forehead involvement = ? causes?
Forehead involvement = LMN lesion ``` Cerebellopontine angle tumour Bells palsy Otitis media, RH syndrome Parotid malignant tumour Trauma ``` Systemic = DM, HIV, sarcoid
30
CN7 palsy - forehead sparing = ? causes?
UMN lesion CVA MS SOL
31
Features of cerebellopontine angle tumour
CN 5678 involvement: - DANISH - loss of corneal reflex - facial muscle weakness - vertigo, tinnitus, sensorineural deafness
32
Mx of Bells palsy
``` Conservative: Protect eye - dark glasses, artificial tears, tape eye @ night Medical: PREDNISOLONE w/i 72 hours (if ?VZV give valaciclovir) ``` (Surgery: plastics if no recovery)
33
Prognosis of Bells Palsy
Full recovery = 80% Remainder: delayed recovery or permanent neuro/cosmetic changes
34
Myasthenia Gravis - Ix?
- Tensilon test (improvement w anticholinesterase) - anti-cholinesterase antibodies - EMG - CT thorax (thymoma!!!) - TFTs (graves is common) - Spirometry - esp FVC
35
Findings on inspection of myasthenia gravis
Thymectomy scar Bilateral ptosis Snarl
36
3 ways to assess fatiguability in myasthenia gravis
1. Repeatedly flap arm 2. Ask to count down from 50 3. Ask them to look up --> bilateral ptosis
37
Management of myasthenia gravis
Acute: IVIG/plasmapharesis Chronic: PYRIDOSTIGMINE Thymectomy - of benefit even if no thymoma
38
Important investigation in bilateral proximal muscle weakness that improves on testing
Anti-VGCC | CT thorax: usually a paraneoplastic syndrome due to SCLC!!!
39
In any patient with CN3 palsy, what investigation would u do in all patients
CT angiogram = a sign of a PCA aneurysm
40
Dangerous differentials for Horners syndrome
Apical lung tumour | Carotid artery dissection/aneurysm
41
secondary prevention for stroke/TIA
Optimise RFs (smoking, wt loss, HTN, DM) STATIN (everyone) Clopidogrel 75mg OD for everyone unless on anticoagulation Warfarin/NOAC: if cardioembolic stroke/AFib/venous sinus thrombosis/dissection
42
Causes of foot drop? | Associated sensory features
Fibular head trauma Sitting cross legged Loss of sensation along lateral lower leg
43
What nerve is at risk of damage in distal humerus fracture? | Presentation?
Ulnar nerve Weakness of finger abduction Ulnar claw - flexed 4th and 5th finger - ONLY if lesion is close to rist Can't do 'good luck' sign Loss of sensation in ulnar 1.5 fingers
44
Weak elbow extension | wrist drop
Radial nerve damage at the axilla
45
Wrist drop + finger drop
Lesion is of radial nerve, at the humerus
46
Waiters tip - where is the lesion? cause?
C56 i.e. higher brachial plexus | - shoulder dystocia
47
Ulnar paradox
Ulnar claw is worse the more distal the lesion is: close to wrist: medial lumbricals weakened -- > 4+5th fingers flexed More proximal: Flexor dig prof weakened --> 4+5th fingers less flexed!
48
Wasting of dorsal muscles of hand Claw hand Lesion? Cause?
Lower brachial plexus injury (C8T1) Cause: trauma from suddenly arm is pulled superiorly (tree) OR Apical lung tumour --> T1 involvement
49
Causes of a raised hemidiaphragm - where is the lesion? what causes it?
Phrenic nerve palsy (C3-5) ``` Neoplasm: - lung, thymoma, myeloma Mechanical: - Cervical spondylosis Infective: - Zoster, HIV, TB, Lyme ```
50
2 or more peripheral nerve palsies - what is this phenomenon called? And what can cause it?
Mononeuritis multiplex ``` WARDS PLC (most common = DM) Wegeners, Amyloid, RA, DM, Sarcoid, PAN, Leprosy, Cancer ```
51
Ddx for vertigo
IMBALANCE - Infection: Ramsay Hunt, labrynthitis (post URTI) - Meniere's (tinnitus, SNHL, N+V) - BBPV (positional) - Amino glycosides (gent) - Arterial: Stroke, migraine - Nerve: Acoustic Neuroma - Central: MS, SOL - Epilepsy
52
TACS criteria for stroke - what is it for? what are the criteria?
Anterior circulation stroke - Homonymous hemianopia - Hemparesis OR sensory deficit - Higher cortical dysfunction: dysphasia or hemispatial neglect
53
Define a posterior circulation stroke
Haemorrhage or infarct of the vertebral arteries or basilar artery or its branches
54
Presentations of posterior circulation stroke
Cerebellar syndrome Brainstem syndrome Homonymous hemianopia (occipital lobe involvement)
55
Define lacunar stroke (i.e. what structures are affected
Small infarcts in blood supply to internal capsule, basal ganglia, thalamus absence of brainstem signs/higher cortical dysfunction/drowsiness/homonymous hemianopia
56
Absent corneal reflex in R eye + Loss of pain sensation in L arm and leg diagnosis? other features?
R sided lateral medullary syndrome i.e. infarct in post inf cerebellar artery or vertebral artery Other features: dysphagia, dysarthria, ataxia, nystagmus, Horners syndrome
57
Pupil - constricted + doesn't react to light + DOES accommodate
Argyll Robertson pupil DM or neurosyphilis
58
Pupil - fixed and dilated + doesn't respond to light or accomodation
Holmes Adie Often viral cause
59
Features of temporal lobe- focal seizure
Automatisms (lip smacking) Hallucinations (olfactory) Emotional disturbance Deja vu/jamais vu
60
ITP - platelet count? clotting times?
Low platelets | Normal APTT and PT
61
Common long term complication o meningitis
SN hearing loss
62
Pt takes metoclopramide for post-op nausea - retracted eyelids, fixed upward gaze, neck writhing --> dx? mx?
Oculogyric crisis | Mx = procyclidine
63
Why be careful of rapid correction of hyponatremia
Central pontine myelinolysis | -
64
Ring enhancing lesions on CT
toxoplasmosis
65
ROmbergs test - what does it tell you?!
+ve = sensory ataxia defect w vision/vestibular system/proprioception -ve = ataxia is likely due to cerebellar syndreom
66
Bilateral cerebellar signs - likely cause?
global cause - EtOH - MS - phenytoin
67
Causes of cerebellar syndrome
``` Vascular: posterior circulation stroke MS EtOH SOL: CPA tumour Wilsons Phenytoin MSA ```
68
Nystagmus in cerebellar syndrome
Nystagmus is worse when looking towards the same side as lesion
69
Differentials for conductive deafness
Outer ear: FB, wax TM perforation: trauma, infection Middle ear: effusion
70
Differentials for SN hearing loss
- Presbycusis (age related) - Drugs: gentamicin, vancomycin - Infection: meningitis, measles - Menieres - Malignancy: CPA lesion - Paget's (CN8 invasion)
71
Fx of CN4 palsy
Failure to depress the eye on adduction Diplopia is v bad on looking down + in
72
Failure to depress the eye on adduction | Dx? what else may be seen on inspection
CN4 palsy Ocular torticollis
73
Intranuclear ophthalmoplegia = explain
Lesion in MLF (v myelinated) Ipsilateral eye fails to adduct, contralateral eye has nystagmus on abduction MLF connects CN3 + CN6 nuclei - on lateral gaze, output to CN3 and CN6 is initiated via MLF
74
Causes of CN3 palsy
PCA aneurysm MS SOL DM, compression
75
Ix in simple palsies --> opthalmoplegia
FBC (infection) Glucose, HbA1c (DM) MRI head (aneurysm) CT head (haemorrhage)
76
Type of imaging for MS?
gadolinium enhancing MRI
77
Presentation of MS
Paraesthesia Optic neuritis (loss of central and colour vision + painful eye) Ataxia + cerebellar signs Motor: spastic paraparesis
78
Features of MS
``` Paraesthesia Spastic paraparesis Transverse myelitis --> bilateral sensory, motor + autonomic Sx Urinary retention, constipation Optic neuritis, INO CEREBELLAR: falls, ataxia, tremor ```
79
Ix in MS
Bloods: autoantibodies MOB and MBP Imaging: Gadolinium enhancing MRI LP: IgG oligoclonal bands Evoked potentials
80
Mx of MS
Acute attack: methylprednisolone Preventing attacks: - IFNbeta + mAbs = alemtezumab Symptomatic: - Amitryptiline (pain) - Clonazepam (tremor) - Self catheterisation/oxybutynin - Physio + baclofen (spasticity)
81
Glucose levels in CSF: normal? Bacterial meningitis? TB meningitis? Protein levels in CSF>?
Normal = 60-70% plasma glucose. Protein <1 Bacterial <50% of plasma glucose. protein >1 TB <50% of plasma glucose. protein 1-5!!!
82
LP in encephalitis LP in viral meningitis
Encephalitis: moderately low glucose high protein + lymphocytes Viral meningitis: Normal glucose (>50% plasma) Protein <1 high WCC
83
Surgical Mx of subdural
Burr Hole Craniostomy
84
Surgical mx of extradural
Craniectomy
85
Mx of SAH
1) urgent neurosurgical referral 2) monitor Obs + repeat CT head if deteriorating 3) aim for SBP >160 4) NIMODIPINE 60mg/4 hrs for 3 weeks 5) CT angio --> Surgical CLIPPING or COIL EMBOLISATION 6) STOOL SOFTENERS, analgesia, antitussives
86
RFs for intracranial venous thrombosis
``` Young Malignancy Thrombophilia Pregnancy, OCP Local infection - otitis, sinusitis, meningitis ```
87
Why does cerebral venous thrombosis --> increased ICP? Why does CVT present like a stroke?
Cerebral veins lie in the subarachnoid space. therefore when they thrombose + occlude --> reduced CSF drainage --> raised ICP When cerebral veins thrombus --> increased pressure in veins + blood stasis --> less oxygen to brain tissue and cerebral edema
88
clinical features of Cerebral venous thrombosis
- Raised ICP: headache, visual changes, papilloedema - Focal deficits: hemiparesis (reduced oxygenation of brain tissue) - Seizures - Encephalopathy
89
Ix for ?cerebral venous thrombosis
CT head MRI head - T2 weighted CT venography LP