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334 Cards in this Set

  • Front
  • Back

What is Amaurosis Fugax?

Temporary occlusion of the RETINAL artery


"feels like curtain descending"

3 most common causes of TIA?

Atherothromboembolism from Carotid



Cardioembolism = Mural thrombus post MI / AF/ Valve Disease/ Prosthetic Valve



Hyperviscosity = Polycythaemia / Sickle Cell / Myeloma

3 most common differential diagnosis for a TIA?

Hypoglycaemia


Migraine Aura


Focal seizure

Investigations for a TIA?

Blood glucose


FBC


ECG


Carotid Doppler + MRI/Angiography

What is the risk of stroke after TIA criteria called?

ABCD2



Age > 60


Blood pressure (Systolic >140 or Diastolic >90)


Clinical Features


Duration (10-59 or 60>)


Diabetes



Greater than 4 points = referral in 24 hours

Management of TIA

1) Control CV risk factors (BP/Cholesterol/Smoking/DM)



2) Anti-Platelets = Aspirin / Dipyridamole (ONLY FOR TIA/ POST MI)



3) Warfarin = IF cardiac embolic - AF/mitral stenosis/ septal MI)



4) Carotid Endarterectomy

What is the different types of stroke classification?

Bamford Classification / Oxford Stroke Classiciation

What are the four types of strokes

TACS


PACS


POCS


LACS

What is TACS

Total Anterior Circulation Stroke


All 3


1) Unilateral Weakness of Face + Arm+ Leg (+/- sensory deficit)


2) Homonymous Hemianopia


3) Higher cerebral dysfunction


(Dysphasia/Visualspatial disorder)


What is PACS

Partial Anterior Circulation Stroke


2/3 of



1) Unilateral Weakness of Face + Arm + Leg (+/- sensory deficit)


2) Homonymous Hemianopia


3) Higher cerebral dysfunction (Dysphasia/Visuosparial disorder)

What is POCS?

Posterior Circulation Syndrome


1/3 of



1) Cerebellar of Brainstem Syndrome


2) Loss of consciousness


3) Isolated Homonymous Hemianopia

What is LACS

Lacunar Syndrome (Basal Ganglia/ Internal Capsule/ Thalamus/ Pons)



CS-PAP



1) Clumsy hand dysarthria


2) Sensorimotor stroke


3) Pure Motor stroke


4) Ataxic hemiparesis


5) Pure sensory stroke

4 Most common causes of a stroke?

1) Small Vessel Occlusion / Cerebral Microangiopathy


2) Cardiac Emboli


3) Atherothromboembolism


4) CNS bleeds (Increased BP/Trauma/Aneurysm Rupture/Anti-Coagulants)

Other rarer causes of stroke

Watershed stroke (BP drop by >40 mmHg)


Carotid Artery Dissection


Vasculitis


Subarachnoid Haemorrhage


Venous Sinus Thrombosis


Antiphospholipid Syndrome


Paradoxial Emboli (ASD/VSD)

What stroke symptoms would make you think of a haemorrhagic stroke?

Meningism


Severe headache coma


3 types of stroke

Cerebral Infarct


Brain stem infarct


Lacunar Infarct

What happens in a cerebral infarct

Contralateral sensory loss OR hemiplegia - initially FLACCID (about 1 hour) before SPASTIC (UMN lesion)



Dysphasia/Homonymous hemianopia/ Visuo-spatial deficit

What happens in a brain stem infarct

QUADRIPLEGIA / Disturbance of gaze and vision / Locked-In Syndrome



Pseudo-bulbar palsy = CN9-12 affected due to stroke

What happens in a lacunar infarct?

Affects the: Pons/Basal Ganglia/ Thalamus/ Internal Capsule


CS-PAP


1) Clumsy Hand Dysarthria


2) Sensorimotor Stroke


3) Pure motor stroke


4) Ataxic Hemiplegia


5) Pure sensory stroke

4 differential diagnosis for a stroke?

Head injury


Hypoglycaemia


Subdural haemorrhage


Hemiplegic Migraine

What is the first hour management plan for stroke?

Protect Airway


Blood Glucose


Urgent CT Head


IV Alteplase (once haemorrhagic is ruled out) within 4.5 hours of a stroke


Nil by mouth


Aspirin (After haemorrhagic ruled out)


Contraindications of IV Alteplase


Previous CNS bleed


AVM


Aneurysm


Varices


Portal hypertension

If a patient has prosthetic valves, what must you give them as primary prevention for a stroke?

Warfarin

What is the name of the scoring system used to predict whether AF will cause a stroke?

CHA2DS2-VASc Score

If the CHA2DS2-VASc score is 0 or >1 what do you give as prophylaxis?

0 = Aspirin/ Nothing


>1 = Warfarin

7 cardiac causes of a stroke?

1) Non valvular AF


2) Prosthetic Valve


3) Post MI


4) External cardioversion


5) Cardiac Surgery - e.g. bypass graft


6) Paradoxical systemic emboli


7) Valve vegetation from Subacute Bacterial Endocarditis/IE

What is the secondary prevention for a stroke? (After adjusting modifiable risk factors)

1) Copidogrel ONLY (P2Y12 inhibitor)


2) Warfarin (if indicated - e.g. prosthetic valve / CHA2D2-VASc >1)

Investigations for causes of a stroke?

1) Hypertension? - retinopathy/nephropathy/CXR


2) Cardiac source? - 24 hour ECG/ECHO


3) Carotid Artery Stenosis? Carotid Doppler USS + CT/MRI Angiography


4) Hypo/hyperglycaemia - Dyslipidaemia - Hyperhomocyteinaemia


5) Vasculitis? ESR/ANA


6) Prothrombic state? Thrombophilia / Antiphospholipid syndrome


7) Hyperviscosity = Polycythaemia / Sickle Cell Disease


8) Genetic Tests = CADASIL/Fabry's Disease

4 complications of a stroke

Aspiration Pneumonia


Pressure sores


Constipation


Depression

How do you manage a patient non-medically after a stroke?

BARTHEL'S index of activities of daily living



- Enablement Approach = Agree to tasks/ plan steps - agree to goals/ review goals



- Make physio fun - swimming/music/videogames

2 most common causes of Sub-Arachnoid Haemorrhage?

1) Rupture of a Saccular Aneurysm (80%)


2) Arterio-venous malformations

5 risk factors of an SAH

Hypertension


Smoking


Alcohol misuse


Bleeding disorders


Microcytic Aneurysm

3 most common sites for a saccular aneurysm

JUNCTION of ANTERIOR communicating artery and ANTERIOR cerebral artery


 


JUNCTION of POSTERIOR communicating artery and internal carotid


 


BIFURCATION of the MIDDLE cerebral artery 

JUNCTION of ANTERIOR communicating artery and ANTERIOR cerebral artery



JUNCTION of POSTERIOR communicating artery and internal carotid



BIFURCATION of the MIDDLE cerebral artery

3 causes of saccular aneurysms ?

ADPKD


Ehlers- Danlos


Coarctation of the aorta

Symptoms of SAH?

Sudden occipital headache (thunderclap - hit in the back of the head)


Vomiting


Collapse


Seizures


Coma/Drowsiness


Neck stiffness


Kernig's Sign

What is TERSON'S Syndrome?

Retinal/Subhyaloid/Vitreous bleeds

What may a person with an SAH feel before the headache

Sentinel headache = warning headache a few days before

Investigations for an SAH

1) CT scan within 48 hours


2) Lumbar puncture = IF CT is negative and NO contraindications AFTER 12 hours


x 3 times = should see XANTHOCHROMIA (yellow due to bilirubin)

Management of SAH?

If proven = Immediate Neurosurgery


Re-examine CNS / Keep Hydrated



NIMODIPINE (Ca2+ antagonists - reduced vasospasm in coronary arteries)



CT Angiography --> Endovascular coiling / Surgical clipping / Intracranial stents

4 complications of SAH

Rebleed


Hyponatraemia


Hydrocephalus


Cerebral ischaemia

Subdural Haemorrhage - what blood vessels/ what shape on CT/ where?

Bridging veins between cortex and venous sinuses


Sickle/Crescent Shape (S=S)


Haematoma between DURA and ARACHNOID

What happens in a subdural haemorrhage?

Gradual rise in ICP


Shifts mid-line structures AWAY from the side of the clot = eventual tentorial herniation & coning

Risk Factors for a SUB-DURAL haemorrhage?

Elderly (brain atrophy makes bridging veins more vulnerable)


Falls (Alcoholics/ Epileptics)


Anticoagulation

Symptoms of Subdural haemorrhage

Fluctuating levels of consciousness


Physical or intellectual slowing


Sleepiness


Headache


Personality Change



Raised ICP


Seizures

Investigations for a subdural haemorrage?

CT scan = Clot (Sickle/Crescent shaped) + midline shift

Management of Subdural Haemorrhage?

Irrigation via Burr Twist Drill & Burr Hole Craniostomy

Where does an extra-dural haemorrhage occur? What blood vessel?

Between the dura and skull


Middle meningeal artery AND vein


Most common cause of an extra-dural haemorrhage

Fractured Temporal or Parietal Bone - typically after trauma

Clinical Features of an ExtraDural Haemorrhage

After head injury - conscious level falls


LUCID INTERVAL - may last up to days before a decrease in the GCS due to a raised ICP



Severe headache / vomiting / confusion / fits


Hemiparesis with brisk reflexes + upgoing plantar

What are the complications of an extra-dural haemorrhage if the bleeding continues?

Ipsilateral pupil dilatation


Coma


Bilateral limb weakness


Death

Investigations for an extra-dural haemorrhage

CT = Biconvex/Lens-shaped haematome

Management of Extra-Dural Haemorrhage

Clot Evacuation + Ligation of Bleeding Vessel


Mannitol (Do decrease raised ICP)

Define a seizure?

Recurrent tendency to spontaneous/intermittent/abnormal electrical activities in parts of the brain = SEIZURES

What are the 3 elements of a seizure?

1) Prodrome


2) Aura = part of the seizure when the patient is aware (Deja-Vu/Jamais-Vu/Strange smells/Flashing lights) - implies a FOCAL seizure


3) Post-Ictally


Headache/confusion/myalgia/sore tongue


Temporary weakness after a focal seizure in the motor cortex (Todd's Palsy)


Dysphasia following focal seizure in temporal lobe

What are the three types of partial seizures?

Partial Seizure = Focal onset with features referable to part of one section



1) Simple Partial Seizure


2) Complex Partial Seizure


3) Partial Seizures with secondary generalisation

What happens in a simple partial seizure?

UNIMPAIRED awareness


Focal/motor/sensory/autonomic/psychic disturbance


NO post-ictal seizures

What happens in a complex partial seizure?

IMPAIRED awareness


Most common from the temporal lobe = Post Ictal Confusion


Rapid recovery after seizures = Frontal Lobe

What happens in partial seizures with secondary generalisation?

Electrical disturbance = focal --> wide = secondary generalised

What are the classical symptoms of a TEMPORAL LOBE partial seizure?

1) Automatisms (Lip-smacking / singing / kissing)


2) Abdominal rising sensation / pain


3) Dysphasia


4) Deja-vu/Jamais vu


5) Hippocampal involvement = Emotional disturbances (terror/panic/anger)


6) Uncal involvement = Auditory/Smell/Taste hallucinations

What are the classical symptoms of a FRONTAL LOBE partial seizure?

1) Motor Features = Peddling legs / posturing


2) Jacksonian March --> Todd's Paralysis


3) Motor Arrest


4) Subtle behaviour disturbances


5) Dysphasia or speech arrest

What are the classical symptoms of a PARIETAL LOBE partial seizure?

1) Sensory disturbances = tingling / numbness


2) Motor symptoms = due to spread to pre-central gyrus

What are the classical symptoms of an OCCIPITAL LOBE partial seizure?

Visual phenomena / Spots - Lines - Flashes

5 types of primary generalised seizures?

1) Absence (usually children)


2) Tonic-Clonic Seizures


3) Myoclonic Seizures


5) Atonic (akinetic) seizures


5) Infantile Spasms (Associated with tuberous sclerosis)

What are absence seizures (Petit mal)?

Usually last for under 10 seconds - usually children


Child suddenly PAUSE - stops mid-sentence - then carries on

What are Tonic-Clonic Seizures (Grand-mal)?

Loss of awareness


Limbs stiffen (TONIC) --> Jerk (CLONIC)


May have one without the other


Post-ictal confusion and drowsiness

What are MYOCLONIC seizures

Sudden JERK of a limb/face or trunk


Either patient suddenly is thrown onto the ground or has a VIOLENTLY DISOBEDIENT limb

What is an Atonic (akinetic) seizure?

Sudden loss of muscle tone = FALL (no lose of consciousness)

If you're diagnosed with epilepsy - what do you have to tell the DVLA?

Cannot drive until seizure free for >1 year

Causes of Epilepsy?

Idiopathic


Cortical scarring


Space-occupying lesions


Stroke


Vascular malformations


Tuberous sclerosis


SLE


Sarcoidosis

Non-epileptic causes of seizures?

Alcohol


Trauma


Stroke


Haemorrhage


Raised ICP

Metabolic disturbance causes of seizures?

Hypoxia


Liver Disease


Infection (Meningitis / Encephalitis/ Syphilis / HIV)


Fever


Drugs (Cocaine / Tramadol)

Management of primary generalised seizures?

1) Generalised Tonic-Clonic Seizures =


Sodium Valporate - Lamotrigine - Toprimate



2) Absence Seizures =


Sodium Valporate - Lamotrigine - Ethosuximide



3) Tonic/Atonic/Myoclonic


Sodium Valporate - Lamotrigine - Toprimate


Management of partial seizures?

CARBAMAZEPINE


Sodium Valporate/ Lamotrigine / Topiramate

Side effects of Sodium Valporate

Nausea + VALPORATE


Appetite increase - weight gain


Liver failure


Pancreatitis


Oedema


Reversible hair loss


Ataxia


Teratogenic (Neural Tube Defects) / Tremor


Encephalopathy

Side effects of LAMOTRIGINE

Maculopapular rash (STEVENS-JOHNSON syndrome)


Hypersensitivity (Fever/DIC)


Vomiting


Diplopia


Blurred Vision


Photosensitivity


Tremor

Side effects of CARBAMAZEPINE?

Leucopenia


Diplopia


Blurred Vision


Impaired balance


Drowsiness

Side effects of Phenytoin?

Nystagmus


Diplopia


Depression


Decreased intellect


Acne


Gum hypertrophy

What is non-epileptic attack disorder?

Uncontrollable symptoms


No learning disabilities


CT/MRI/EEG = All normal

How do you investigate Seizures?

Bloods/LP


EEG (Normal between attacks)


CT + Enhancement


MEG


PET


Ictal SPECT

How do you manage epilepsy if an epileptogenic focus can be identified? (e.g. hippocampal sclerosis or small low grade tumour?)

Neurosurgical resection


Vagal nerve stimulation

What is Status Epilepticus?

Seizure lasting >30 minutes OR repeated seizures without intervening consciousness

Name 2 percipitating factors for status epilepticus?

Alcohol


Stopping medication


Pre-Eclampsia (If pregnant)


How do you treat Status epilepticus?

100% Oxygen


IV Lorazepam x 2


Rectal Diazepam


Buccal Midazolam


Phenytoin/Diazepam infusion


Dexamethason

3 Cardinal Symptoms of PARKINSONISM

(RAT)


Rigidity/ Tone = "Cog-Wheel" / "Lead-Pipe" Rigidity - Increase in tone in limbs + trunk


Limb resists THROUGHOUT movement



Bradykinesia / Hypokinesia = Slow to initiate movement / Stoop / Micrographia/ Lessened Arm swing/ FESTINANCE (shuffling steps) / Freezing at obstacles/ HYPOMIMIA




Tremor = 4-7Hz RESTING - "pill-rolling" thumb & fingers - IMPROVED by voluntary movement/ worse by anxiety

5 Causes of Parkinsonism

1) Idiopathic Parkinson's Disease (Mutation in Fbx07) (Fbitches x 07)


2) Drugs (Neuroleptics / Metoclopramide)


3) Wilson's


4) HIV


5) Trauma

Non motor features of Parkinson's Disease?

REM sleep disorders


Prosody


Constipation


Frequency


Dementia


Decreased sense of smell


Visual Hallucinations


Depression

Pathology behind IPD?

Mitochondrial DNA dysfunction causes a degeneration of the dopaminergic neurones in the substantia nigra pars compacta (associated with Lewy Bodies) = Lowered striatal dopamine levels

Management of IPD?

MDT Meeting Involvement =


GP


Neurologist


PD Nurse


Social Worker


Carers


Physiotherapist


Occupational therapist

Management of IPD?
1) LevoDopa + Benserazide (Dopa-decarboxylase inhibitor) = CO-BENELDOPA
SE = Nausea and Vomiting (Give Domperidone)
Efficacy reduced with time/psychosis/visual hallucinations/painful dystonias

Carbedopa + LevoDopa

2) Dopamine Agonists (ROPINOROLE)
SE = Pathological gambling / compulsive shopping

3) MAO-B Inhibitors (SELEGILINE)
SE = Postural Hypotension

4) COMT Inhibitors (TOLCAPONE)
SE = Severe hepatic complications

Other management ideas for PD?

1) Anticholinergics - for tremor = BENZHEXOL


2) APOMORPHINE (DA agonist - rescue pen)


3) Depression? SSRI


4) Disease Psychosis? OLANZAPINE


5) Respite Care


6) Deep brain stimulation


7) Surgical ablation of overactive subthalamic nuclei

Mneumonic for remembering 5 key symptoms of IPD?

SMART


Shuffling Gate


Mask-like facies


Akinesia


Rigidity


Tremor

5 Parkinson's Plus Syndrome

Parkinsonism + Evidence of separate pathology


PMLVC (Parkinson's Makes Life Very Crap)



Progressive Supranuclear Palsy


Multiple System Atrophy (Shy-Drager)


Lewey Body Dementia


Vascular Parkinsonism


Cortico-Basal Degeneration

5 Parkinson's Plus Syndrome plus VIVID signs

VIVID


Progressive supranuclear palsy = Vertical gaze palsy


Multiple System Atrophy = Impotence / Incontinence


Lewey Body Dementia = Visual Hallucinations


Cortico-Basal Degeneration = Autonomous Interfering Activity


Vascular Dementia = In Diabetics

Define Huntington's Disease?

Autosomal DOMINANT condition affecting the corpus striatum and cortex = incurable/progressive/neurodegenerative disorder

Pathology behind Huntington's Disease

Atrophy and Neuronal Loss of CORPUS STRIATUM AND CORTEX


Expansion of CAG repeats on Ch4



= Depletion of GABA and Acetylcholine


BUT SPARES DOPAMINE

Clinical Features of Huntington's?

Irritability/Depression/Incoordination --> Chorea --> Dementia + Fits ---> Death

What is Chorea?

Continuous flow of jerky, quasi-purposive movement


Fleeting from one part of the body to the other

Investigation and Management for Huntingtons?

MRI = Ventricularmegaly


NO CURE - only symptomatic



Chorea = Neuroleptics


Depression = Seroxate


Aggression = Haloperidol

7 Classical Features of DEMENTIA

MAHAWAM


MEMORY LOSS


Agitation


Hallucinations


Aggression


Wandering


Apathy


Mood Disturbances

2 Diagnostic Tests for Dementia?

AMT


Addenbrooke's Cognitive Examination


4 Main Types of Dementia?

A VERY LOVELY FRIEND



Alzheimer's


Vascular Dementia


Lewey Body Dementia


Fronto-Temporal Dementia

Describe Vascular Dementia

Cumulative effects of MANY small strokes


Thus - SUDDEN ONSET and STEP-WISE deterioration is characteristic



Look for evidence of vascular pathology = HTN/Past strokes/ Focal CNS signs

Describe Lewy Body Dementia

Typically FLUCTUATING cognitive impairment


Detailed Visual Hallucinations - Small Animals / Children



Histologically = Lewy Bodies in BRAINSTEM & Neocortex

Decribe Fronto-Temporal Dementia

Contains PICK inclusion bodies


Executive impairment


Behavioural/Personality Change


Disinhibition


Hypeorality


Emotional Unconcern

5 other causes of dementia?

HIV


HD


IPD


Whipple's


Repeated Head Trauma

Clinical Features of Alzheimer's

MAVEV ---> BIMAL



Memory loss


Anosognosia


Verbal Abilities


Executive Function


Visuo-spatial skills




Behavioural Change (aggression/wandering)


Irritability


Mood disturbance (depression)


Agnosia


Hallucinations/Dellusions (Psychosis)

Pathogenesis behind Alzheimer's disease?

Accumulation of B-amyloid peptide --> Progressive Neuronal Damage



NEUROFIBRILLARY TRIANGLES


B-AMYLOID PLAQUES


TAU PROTEINS


Decreased Acetylcholine



Neuronal Loss is Selective = Hippocampus/Amygdala/Temporal neocortex

RISK Factors of Alzheimer's

Down's Syndrome


1st Degree Relative


Depression


Loneliness

Management of Alzheimers Disease
1) Referral to memory service
2) Acetylcholinesterase inhibitors = RIVASTIGMINE
SE = D&V/Cramps/Headache/Insomnia

3) NMDA inhibitor=
MEMANTINE
SE = Hallucinations / Confusion / Hypertonia

4) Sensation stimulation/ CBT/Cognitive stimulation programmes/ Massage/ Dance therapies

8 Issues in managing someone with dementia?

1) Care Coordinator? Laundry/DayCare/Priority Parking


2) Capacity to make decisions?


3) MUST develop a routine


4) PLAN AHEAD - DO NOT MOVE HOUSE


5) Day Care


6) Care for the carers?


7) Challenging Behaviour? Lorazepam


8) Depression? Citalopram

What is the difference between common and classic migraines?

Common = Migraine WITHOUT aura


Classic = Migraine WITH aura

Define migraine

Episodic severe headaches with/without aura


Often prementrual


Usually Unilateral with NAUSEA/VOMITING +/- Photo/phonophobia

What 4 auras can occur in migraine?

Visual = Chaotic cascading / Distorting / Dots / Zigzags / Scotomata hemianopia



Somatosensory = Paraesthesiae = fingers -->face



Motor = Dysarthria / Ataxia/ Opthalmoplegia / Hemiparesis



Speech = Dysphasia / Paraphasia

Pathophysiology of Migraine?

Cortical spreading depression


Altered modulation of normal sensory stimuli + trigeminal nerve dysfunction

What is the diagnostic criteria for a NON-migraine aura?

>5 Headaches (Lasting 4-72 hours + N&V (or Photo/phonophobia)


AND


2 of : Unilateral - Pulsating - Worsened by routine activity

Triggers of a migraine?

CHOCOLATE



Caffeine


Hangovers


Orgasms


Cheese


Oral contraception


Lie-In


Alcohol


Tireness


Exercise/Emotions


Management of a migraine?

1) NSAIDS (Ketoprofen)


2) Oral 5HT Agonists (Sumatriptan)


CI = IHD/Coronary Spasm


3) Ergotamine


SE = Gangrene


4) 12-weekly Botulinim Toxin Type A


5) Warm/Cold Packs

Prophylaxis for Migraine?

Avoid Triggers


IF over 2x per month AND not responding to treatment =



1) Propanolol


2) Amitriptyline


3) Topiramate


4) Valporate

What facial pain has post-nasal drip/ dull constant ache over the face / worse pain on bending over?

SINUSITIS

What happens in acute glaucoma?

Occurs in the elderly/long-sighted


Constant aching pain - develops around one eye - radiates to forehead


CF = Cloudy cornea/decreased acuity/red eye/N&V/ haloes


Percipitating Factors = Dilating Eye drops/ emotional upset/ sitting in the dark



Rx = IV ACETAZOLAMIDE

Describe a tension headache?

Tight band around the head


BILATERAL


Non-pulsatile headache + scalp muscle tenderness



Rx = Explanation/Reassurance/ Withdraw analgesics / Massage/ AMITRIPTYLINE

4 things that make raised intracranial pressure headaches worse?

Walking


Lying


Bending forward


Coughing

4 symptoms associated with raised intracranial pressure?

Vomitting


Papilloedema


Seizures


Odd behaviour


Alleviated by standing

Investigations for suspected raised intracranial pressure?

CT Head = EXCLUDE space occupying lesion


Consider idiopathic intracranial hypertension



NO NO NO LUMBAR PUNCTURE

Management for raised ICP

Lose Weight


Mannitol

Tell me a bit about medication overuse (analgesic rebound) headache?

Causes by mixed analgesics usually (paracetamol + codeine / opiates)


Also Ergotamine/ triptans



Management of medication overuse headache?

Withdraw analgesia + aspirin


After = Valporate/Gabapentin



Inform them - no more than 6 painkillers a month

Causes of Cluster Headache?

Superficial temporal artery smooth muscle hyper-reactivity to 5HT


ALSO hypothalamic grey matter abnormalities

Clinical Features of Cluster Headaches?

Rapid-onset of EXCRUCIATING pain around one eye


Watery & Bloodshot / Lid swelling/ Lacrimation/ Facial Flushing/ Rhinorrhoea / Miosis + Ptosis



STRICTLY unilateral


Management of Cluster Headaches?

100% OXYGEN


SC Sumatriptan / ZOLMITRIPTAN nasal spray

2 preventative treatments for cluster headache?

Sub-occipital steroid injections


Verapamil


Lithium

What is Trigeminal Neuralgia? Where do you most often get it?

Paroxysms of intense STABBING pain - lasting seconds in trigeminal nerve distribution


MOSTLY Mandibular & Maxillary



- Face screws up with pain (Tic Doloureux)

5 Triggers for Trigeminal Neuralgia

WASTED



WAshing


Shaving


Talking


Eating


Dental prostheses

Causes of Trigerminal Neuralgia

1) Compression of nerve root = Anomalous or Aneurysmal intracranial vessels/tumour



2) Chronic meningeal inflammation



3) MS



4) Skull base malformation


Management of Trigerminal Neuralgia?

CARBAMAZEPINE


Lamotrigine



Surgical = Microvascular Decompression / Thermocoagulation of trigeminal ganglion

What age group does GCA normally affect?

OVER 60


If under 55 - think Takayasu's Arteritis


d

Define Giant Cell Arteritis

Granulomatous arteritis of unknown aetiology - associated with Polymyalgia Rheumatica

Clinical Features of GCA

Headache


Temporal artery & scalp tenderness (when combing hair)


Jaw Claudication


Amaurosis Fugax OR sudden blindness (central retinal artery)

Extracranial symptoms of GCA?

Dyspnoea


Morning Stiffness


Unequal or weak pulses


Weight loss


Malaise


Fever

What do you see on examination of the superficial temporal artery in GCA?

Tender


Firm


Pulseless

Investigations for GCA

ESR&CRP UP UP UP UP


Raised Platelets and Alk Phos



TEMPORAL ARTERY BIOPSY within 7 days of steroids

Management of GCA

PREDNISOLONE RIGHT AWAY


Also:


PPI's


Bisphosphonates

What is Polymyalgia Rheumatica?

>50 years old


Subacute onset (<2 weeks)


Bilateral aching tenderness


Morning stiffness in SHOULDERS and PROXIMAL LIMB MUSCLES (Pelvic Girdle?)



Also:


Mild polyarthritis / Tensosynovitis / Carpal Tunnel Syndrome


Fatigue / Fever/ Weight loss/ Anorexia

Investigations for PMR

Raised ESR/CRP/ALP

Management of PMR?

PREDNISOLONE


= Dramatic response within 1 week

Where is the lesion if there is paraplegia?


Hemiplegia?

Paraplegia = Cord compression


Hemiplegia = Brain lesion

Clinical Features of Spinal Cord Compression?

Spinal/Nerve root dull ache pain


Leg weakness/sensory loss


Arm weakness (suggests cervical cord lesion)


Bladder and anal sphincter involvement = LATE symptom

What are typical LMN signs?

Decreased tone


Decreased reflexes


Wasting


Fasciculations

What are typical UMN signs?

Increased tone


Brisk reflexes


Weakness in EXTENSORS (bent arm post stroke)

Cord compression will produce UMN or LMN?

LMN at the level of the lesion


UMN signs below

7 Causes of Spinal Cord compression

1) SECONDARY MALIGNANCY (BBTKP)


2) Infection (Epidural Abscess)


3) Cervical Disc prolapse


4) Haematoma (warfarin?)


5) Intrinsic cord tumour


6) Myeloma


7) Spinal TB (Pott's Disease)

Differential Diagnosis for spinal cord compression?

Transverse myelitis


MS


Cord vasculitis


Trauma


Dissecting Aneurysm

Investigations for spinal cord compresssion?

IMMEDIATE MRI

Management of Spinal Cord Compression?

If secondary to a malignancy?
IV DEXAMETHASONE + Chemo/Radio



Epidural abscess? Decompression + Antibiotics



Decompressive Laminectomy

Causes of Unilateral Food Drop

DM


Common Peroneal Nerve Palsy


Stroke


Prolapsed Disc


MS

Causes of weak legs with NO sensory loss

MND


Polio


Causes of chronic spastic paraparesis

MS


Cord tumour (astrocytoma)


Cord metastases


MND


Causes of chronic flaccid paraparesis?

Peripheral Neuropathy


Myopathy

Cauda Equina Syndrome - 4 CLASSIC symptoms

1) Bowel/Bladder Dysfunction


2) Decreased sensation in SADDLE area (Perineal)


3) Sexual Dysfunction


4) Neurological deficit in the lower limb = Motor/sensory loss/ reflex change

Causes of Cauda Equina?

L4/L5 --> L5/S1= LUMBAR DISC HERNIATION


Tumours


Epidural Abscess


Congenital (Spina bifida)


Sponylolisthesis


Late stage AS

Other symptoms of cauda equina syndrome?

Lower back / leg pain / motor or sensory deficits


Urinary retention


Saddle & Perineal Anaesthesia


Bowel/Bladder Dysfunction


Asymmetrical weakness with loss of reflexes


Sexual dysfunction

Investigations for Cauda Equina?

MRI MRI MRI MRI MRI

What is the difference between cauda equina and conus medullaris syndrome?

Conus medullaris is located at T12-L2


Associated with urinary retention and constipation


LESS PAINFUL

Management of cauda equina syndrome?

URGENT SURGICAL DECOMPRESSION

Define Multiple Sclerosis?

Discrete PLAQUES of demyelination at multiple CNS sites from T-cell mediated immune response



RELAPSING AND REMITTING


DISSEMINATED IN TIME AND SPACE

What happens after prolonged demyelination?

Axonal Loss


Clinically progressive symptoms

Eye Signs in Multiple Sclerosis


Unilateral Optic neuritis (Pain on eye movement + rapid decreased in central vision)


Diplopia / Hemianopia


BILATERAL INTERNUCLEAR OPTHALMOPLEGIA



Charles Bonnet Syndrome = Decreased Visual Acuity + Hallucinations


Uhthoff's Phenomenon = Decreased vision on exercise/hot meals/ hot bath. Phosphenes (flashed) on eye movement


Pulrich Effect = Unequal Eye Latencies


Argyle Robertson Type Pupil


Sensory Signs in MS?

Lhermitte's Sign = Neck Flexion causes "electric shock in trunk and limbs



Numbness/tingling in limbs


Decreased vibration sense


Trigeminal neuralgia

Motor Signs in MS?

Spastic Weakness (Les?)


Transverse Myelitis = Loss of motor/sensory/autonomic/reflex and sphincter function BELOW the level of the lesion



Devic's Syndrome = Neuromyelitis Optics = Transverse myelitis + Optic atrophy + NMO-IgG antibodies

GI Signs in MS?

Swallowing Disorders


Constipation

Cerebellum Signs in MS?

Trunk and limb ataxia


Intention tremor


Scanning speech


Falls

Sexual/GU signs in MS?

Erectile Dysfunction


Urinary retention


Incontinence

Cognitive / Visuospatial Signs in MS?

Amnesia


Decreased executive functioning


Change in mood

5 signs of POOR prognosis in MS?

Increased AGE


Motor signs at onset


Many relapses early


Axonal loss


Increased MRI lesions

Diagnosis of MS?

Clinical = Lesions Disseminated in TIME&SPACE - with no other viable causes


MRI of brain and spinal cord


CSF = Oligoclonal bands of IgG on electrophoresis NOT present in the serum


Evoked potentials = Delayed visual/auditory/somatosensory

What is the criteria required to diagnose MS?

McDONALD CRITERIA



Attacks must be >1 hour - with 30 days in between

MRI abnormalities seen in MS?

3/4 needed



Gadolinum enhancing


OR


>9 T2 hyperintense lesions



>1 infratentorial lsions


>1 juxtacortical leions


>3 periventricualr lesions

3 antibodies in MS?

NMO-IgG (Devic's Syndrome)


MOG


MBP

Management of MS

MINGA - White Trash 30 year old



Methylprednisolone


Interferon 1-B & Interferon-IA


x = Abortion/ Depression


Natalizumab (Acts against VLA-4 Receptors)


Glatiramer Acetate (Doxorubicin Analogue)


Azathioprine



Palliative Treatment?

Spasticity? Diazepam


Tremor? Botulinum Toxin Type A


Urgency/Frequency? Intermittend Self-Catheterisation

What is Myasthenia Gravis?

Autoimmune disease mediated by ANTIBODIES to nicotinic AchR - interfering with neuromuscular transmission VIA a depletion of post-synaptic receptor sites



MAY BE ASSOCIATED WITH THYMOMA

Pathophysiology in MG?

Antibodies BLOCK the postsynaptic ACh receptors = prevent end plate potential from triggering muscle contraction = MUSCLE WEAKNESS



Acetylcholinesterase then BREAKS down ACh = takes it away

Clinical Features of MG

Increasing muscular fatigue


- Extra-ocular (Ptosis / Diplopia / Peek sign)


- Bulbar


- Face (Myasthenic snarl / Dysphonia / Chewing or Talking difficulties)


- Neck


- Limb girdle



IMPROVES AFTER REST

6 things that worsens weakness in MG?

1) Pregnancy


2) Hypokalaemia


3) Gentamicin


4) Opiates


5) Emotion


6) Exercise


7) Infection


8) Over treatment

Aetiology of MG?

<50 years old = Female/Other AI Diseases/ THYMIC HYPERPLASIA


>50 years old = Male / Thymic Atrophy or Tumour I

Investigations for MG?

Anti-AChR antibody OR MUSK Antibody


Neurophysiology (Evoked Potentials)


CT of Thymus


ICE PACK TEST -ptosis improves by >2mm after Ice pack for >2 minutes


Tensilon Test

Management of MG?

Acetylcholinesterase Inhibitor = PYRIDOSTIGMINE


SE = Lacrimation / Sweats / Vomiting / Diarrhoea



Immunosuppression = PREDNISOLONE + AZATHIOPRINE



THYMECTOMY


- Consider if <50 OR not controlled by Pyridostigmine

What happens during a Myasthenic Crisis?

WEAKNESS OF THE RESPIRATORY MUSCLES


during a relapse - can be life threatening



Must must monitor FVC + Give Ventilatory Support

Management of Myasthenic Crisis?

Plasmapheresis


IV Immunoglobulin

Causes of Lambert-Eaton Myasthenic Syndreom

Paraneoplastic (Small Cell Lung Ca)


Autoimmune

3 clinical signs of LEMS

Gait difficulty FIRST - before eye signs



Autonomic involvement = Dry mouth / constipation / Impotence



Hyporeflexia & Weakness = Improves AFTER exercise


Management of LEMS

IV Immunoglobulin

MND affects which neurones?

MOTOR CORTEX


CRANIAL NERVE NUCLEI


ANTERIOR HORN CELLS

What does MND spare?

Affects BOTH LMN and UMN BUT



1) No Sensory loss or sphincter disturbance (Distinguishes from MS/Polyneuropathies)



2) NEVER affects eye movements


(Distinguishes from MG)

Genetics behind MND?

ALS-FTD locus at Ch9



Or



Autosomal Dominant D90A SOD1 Mutation

4 Clinical Patterns of MND

All Bald Men Shine (ABML)



ALS (Amyotrophic Lateral Sclerosis)


Progressive Bulbar Palsy


Progressive Muscular Atrophy


Primary Lateral Sclerosis

What happens in ALS (Amyotrophic Lateral Sclerosis)

Loss of motor neurones in the MOTOR CORTEX and in the ANTERIOR HORN



Weakness


UMN Signs (Increase Tone/Increased Reflexes/ Upgoing Plantars)


LMN Signs (Wasting / Fasciculation)



Worse prognosis if: Older/Decreased FVC/Bulbar onset

What happens in Progressive Bulbar Palsy?

Only affects CN9-12


See LATERP

What happens in Progressive Muscular Atrophy

ANTERIOR HORN CELL ONLY = No UMN signs


Affects DISTAL muscle groups before proximal



Weakness/Wasting/Fasciulations

What happens in Primary Lateral Sclerosis?

Loss of BETZ cells in motor cortex


UMN signs + Marked Spastic Weakness + Pseudobulbar Palsy

When to think of MND?

>40


Stumbling/Spastic gait


Foot drop + Proximal Myopathy


Weak grip & shoulder abduction


Aspiration pneumonia

How do you diagnose MND?

EL ESCORIAL CRITERIA

Most likely cause of death in MND?

Respiratory Failure due to bulbar palsy + pneumonia

MDT involvement in MND?

Neurologist


Palliative Nurse


Hospice


Physiotherapy


OT


Speech and Language Therapist


Dietician


Social Services

Management for MND

1) Antiglutamateric Drugs (Sodium Channel Blocker)


= RILUZOLE



2) Drooling? =


PROPANTHELINE + AMITRIPTYLINE



3) Dysphagia?


Blended food/ Ng tube



4) Non-invasive ventilation / NSAIDs/ Opiods

What is Bulbar Palsy?

Disease of the NUCLEI of CN9-12 in the medulla

Signs of Bulbar Palsy?

LMN lesions of the tongue and muscles of talking/swallowing


= Flaccid / Fasciculating tongue/ Jaw Jerk Decreased/ Dysphonia / Drooling

Causes of Bulbar Palsy

MND


GBS


Polio


MG

What is Psudobulbar palsy (Corticubulbar palsy)?

More common than Bulbar


UMN lesions of the muscles of swallowing & talking due to BILATERAL lesions above the mid-pons


e.g. Corticobulbar tracts


(MS/MND/STROKE)

Signs of Corticobulbar palsy?

Slow tongue movements with slow deliberate speech


Increased Jaw Jerk


Increased Pharyngeal & Palatal Reflexes


Emotional incontinence = uncontrolled weeping/giggling


Palatal movements absent


Persistent dribbling

Define a TIA

Sudden onset of a focal neurological deficit lasting for less than 24 hours due to an occlusion of part of the cerebral circulation

Define Gullian-Barre Syndrome

Acute inflammatory demyelinating polyneuropathy = symmetrical ascending muscle weakness starts

4 things that can trigger GBS?

Campylobacter Jejuni


CMV


HIV


EBV



= Leads to autoantibody mediated nerve cell damage

Clinical Features of GBS

Progressive onset of LIMB weakness = 4 WEEKS -----> Recovery


- Proximal muscles affected more (e.g. Trunk/Respiratory/Cranial Nerves CN7)


- Pain in back/limbs



DIAGNOSTIC =


PROGRESSIVE WEAKNESS OF ALL 4 LIMBS


AREFLEXIA



Supporting symptoms = Progression over days / symmetrical / CN involvement


What is the main DD for GBS?

MG


Botulism


Poliomyelitis


Chronic Inflammatory Demyelinating Radiculopathy = Slower onset & recovery

What is Miller Fisher Syndrome?

Associated with Anti- GQ1b antibodies in serum



1) Opthalmoplegia


2) Ataxia


3) Areflexia

Investigations for GBS?

1) Nerve Conduction Studies = Slow motor conduction


2) CSF = Increased protein


3) Respiratory Involvement = FVC check every 4 hours


4) Spine MRI

Management of GBS

IV Immunoglobulin ///


CI = in IgA deficiency



Plasma Exchange



Supportive Treatment (Heparin / Physiotherapy / NG Tube)

Causes of Mononeuropathies

Trauma


Entrapment (e.g. tumour)


Acute compression (e.g. common peroneal nerve)

Define Mononeuritis Multiplex

When 2 or more peripheral nerves affects --> tends to be systemic

Causes of Mononeuritis Multiplex

WARDS PLC



Wegener's


Aids


Rheumatoid


DM


Sarcoidosis



PAN


Leprosy


Carcinomatosis

Median Nerve (C6-T1) - Which muscles does it innervate?

LOAF


Lumbricals


Opponens Pollicis


Abducter Pollicis Brevis


Flexor Pollicis Brevis

Hand Examination = Thumb abduction and opposition = which nerve?

Median Nerve

Ulnar Nerve C6-T1 - Most common cause of damage?

Elbow Trauma (Cubital Tunnel / Epicondylar Groove)

5 Signs of Ulnar Nerve Damage

Weakness/wasting of :


1) Medial wrist flexors (ulnar side)


2) Interossi (Cannot cross fingers)


3) Medial two lumbricals (claw hand)


4) Hypothenar eminence



5) Also sensory loss in ulnar distribution

4 ways to treat ulnar nerve damage?

Rest/Avoid pressure


Night time soft elbow splint


Decompression in situ


Medial epicondylectomies

Where does damage to the radial nerve (C5-T1) happen?

Compression against the humerus

Signs of Radial Nerve Damage

SATURDAY NIGHT PALSY


Wrist/Finger drop


Sensory loss at snuff box

What 4 muscles are innervated by the radial nerve?

BEST



Brachoradialis


Extensors


Supinator


Triceps

Clinical features of brachial plexus damage?

Pain/paraesthesiase and weakness in affected arm

Causes of Brachial Plexus damage?

Trauma


Radiotherapy (e.g. for Breast Ca)


Pancoasts Tumour


Cervical Rub

What two clinical features will present with phrenic nerve palsy

C3,4,5 keeps the diaphragm alive



Orthropnoea


Raised hemidiaphragm on CXR

Causes of Phrenic Nerve palsy

Lung carcinoma


Myeloma


Thymoma


Cervical spondylosis


HIV


Lyme disease


TB

What symptoms do you get from damage to the LATERAL cutaneous nerve of the thigh (L2-L3)

Meralgia Paraesthesia


Burning pain on the anterolateral part of the thigh due to entrapment of the nerve under the inguinal ligament

Sciatic Nerve (L4-S3) - Damage from where?

Pelvic tumours or fractures to the pelvis/femur


Lesions affect the hamstrings and all muscles below the kneed (e.g. foot drop)


Loss of sensation below the knee (laterally)

Common Peroneal Nerve Damage (L4-S1) - What happens?

Originates from the SCIATIC nerve just above the knee


Damage is from the FIBULAR head (trauma/sitting cross legged)



FOOT DROP FOOT DROP FOOT DROP


Weak ankle dorsiflexion/eversion


Sensory loss over the dorsum of the foot

What happens in Tibial Nerve Damage

Loss of plantar flexion of the foot (tip toe)


Loss of inversion/flex toes


Sensory loss over the sole

Carpal Tunnel Syndrome affects WHAT nerve?

MEDIAN NERVE - WAKE AND SHAKE WAKE AND SHAKE

Clinical Features of Carpal Tunnel Syndrome?

Aching pain (typically at night)


Paraesthesiae in the thumb / index / middle fingers (relieved by hand shake)


Sensory loss and weakness of Abducter Pollicis ?brevis



Loss of light touch / 2-point discrimination / sweating

Causes of Carpal Tunnel Syndrome

MEDIAN TRAPS



Myxoedema (Hypothyroid)


Enforced flexion


Diabetic neuropathy


Idiopathic


Acromegaly


Neoplasm (Myeloma)



Tumour - Benign (Lipoma)


RA


Amyloidosis


Pregnancy


Sarcoidosis

Investigations for Carpal Tunnel Syndrome?

Neurophysiology


Tinnel's test


Phalen's test

Management of Carpal Tunnel Syndrome?

Splinting


Local Steroid Injection


Decompression Surgery

Classical features of polyneuropathy?

Symmetrical & widespread distribution - distal weakness and sensory loss (glove&stocking)

3 ways to classify polyneuropathy?

Course (acute or chonic - e.g. GBS?)


Function (Sensory/Motor/Autonomic)


Pathology (Demyelination / Axonal degeneration/ Both)



3 causes of MOTOR polyneuropathies

GBS


Charcot-Marie Tooth (Distal wasting below the knees - inverted champagne bottles)


Lead Poisoning

3 causes of SENSORY polyneuropathies

DM


Renal Failure


Leprosy

Causes of Polyneuropathies in general

Metabolic = DM/Renal Failure/ Hypo/Hyper Thyroidism / Hypoglycaemia



Vasculitides: PAN/RA/Wegner's



Malignancy: Polycythaemia Rubra Vera



Inflammatory: GBS/Sarcoidosis



Infections: Syphillis / HIV



Nutritional: Deficiency in Vitamin B1 & B12


Too much OR Too little Vit B6



Drugs: Alcohol/ Isoniazid / Phenytoin

Symptoms of Peripheral Neuropathy?

Sensory = Numbness/ Pins&Needles - glove and stocking/ Trauma or Burns



Motor = Progression/ Weak or clumsy hands / Difficulty in walking/ Breathing difficulty


= LMN lesion symptoms / Decreased FVC

Autonomic Neuropathy Symptoms?

SEE NEXT FEW CARDS

Investigations for polyneuropathy

Nerve Conduction Studies (Demyelinating v axonal causes)


BLOODS - CXR - URINALYSIS - LP + specific genetic tests (PMP22 for charcot)

Management of polyneuropathy

Treat the cause


Involve physiotherapy / OT


Foot care / shoes


Neuropathic Pain? Amitriptyline / Gabapentin

6 causes of autonomic neuropathy

GDL is ASS



GBS


DM


Leprosy



Amyloidosis


Sjogren's


SLE

Clinical features of SYMPATHETIC autonomic neuropathy?

Postural Hypotension


Decreased sweating


Constipation


Horner's

Clinical Features of PARASYMPATHETIC autonomic neuropathy?

Constipation


Nocturnal Diarrhoea


Urine retention


Holmes- Adie pupil

Penis and autonomic neuropathy?

POINT & SHOOT



Parasympathetic = Erectile Dysfunction



Sympathetic = Ejaculatory Failure

Investigations for autonomic neuropathy

BP standing and lying - DROP of >20/10 is abnormal


ECG


Cystometry


Pupils


Paraneoplastic antibodies (Anti-Hu/Anti-Yo/Anti-Ri)

What does Vitamin B1 (THIAMINE) deficiency cause

WERNICKE'S ENCEPHALOPATHY


Classical Triad:


1) Confusion


2) Ataxia


3) Opthalmoplegia (Nystagmus/Lateral Rectus palsy)

Pathology of B1 deficiency

Periaqueductal punctate haemorrhages & focal damage

Causes of Vitamin B1 deficiency?

Chronic Alcoholism


Eating Disorders


Malnutrition

Management of Vitamin B1 deficiency

Can lead Korsakoff's syndrome


IV/IM THIAMINE

What is Vitamin B6?

PYRIDOXINE

What causes Vitamin B6 deficiency? What symptoms can this cause?

Mainly isoniazid therapy for TB - SENSORY NEUROPATHY MOSTLY



Management=


PYRIDOXINE

What can Vitamin B12 deficiency cause?

Subacute combined degeneration of the spinal cord = Insidious onset with peripheral neuropathy

Vitamin B12 deficiency clinical symptoms?

Symmetrical Dorsal Column Loss = Touch/ Propioception/ Vibration & LMN signs



Symmetrical Corticospinal tract loss = Motor & UMN signs




Joint position/Vibration --> Ataxia --> Stiffness --> Weakness

Triad of symptoms in Vitamin B12 deficiency

1) Extensor Plantars (UMN)


2) Absence Knee Jerks (LMN)


3) Absent Ankle Jerks (LMN)



Pain and Temperature IN TACT

Management of Vitamin B12 deficiency?

IM HYDROXOCOBALAMIN

What happens in Brown-Sequard Syndrome?

Hemisection or unilateral cord lesion


Clinical Features of Brown-Sequard?

1) IPSILATERAL UMN weakness below the lesion


** Severed corticospinal tract**


= Spastic paraparesis


= Brisk reflexes


= Extensor plantars



2) IPSILATERAL loss of propioception and vibration


**Severed dorsal column**



3) CONTRALATERAL loss of pain and temperature


**Severed spinothalamic tract that has crossed**

Causes of Brown-Sequard?

Bullet


Tumour


Disc Hernia


Cervical Spondylosis


MS


Myelitis


Septic Emboli



MRI MRI MRI MRI MRI MRI MRI MRI MRI MRI

What is a pontine lesion? What does it cause?

Pons lies above the decussation of the posterior columns



Pontine lesion causes LOSS of ALL forms of sensation on the OPPOSITE side of the lesion

Causes of Cranial Neve Lesions?

DM


Stroke


MS


Tumours


Sarcoidosis


Vasculitis = PAN/SLE


Syphillis

Loss of sense of smell?

CN1 - OLFACTORY NERVE


Causes = Trauma / Respiratory Tract Infection / Meningitis

Loss of Vision?

CN2 - OPTIC NERVE



1) Monocular Blindness = MS/GCA


2) Bilateral Blindness = DM/MS/Neurosyphillis


3) Bitemporal Hemianopia = Optic chiasm compression (Pituitary adenoma/craniopharyngioma/internal carotid aneurysm)


4) Homonymous hemianopia = Stroke/Abscess/Tumour


5) Optic neuritis = Pain on moving eye / loss of central vision / relative afferent pupillary defect/ Disc swelling


6) Papilloedema


Bilateral swollen discs = RAISED ICP / Retro-orbital lesion (e.g. cavernous sinus thrombosis)


7) Optic Atrophy = Pale optic disc/Reduced Acuity = MS/Frontal Tumours


8) Ischaemic Papillopathy = Swelling of disc due to stenosis of posterior ciliary artery = GCA

Causes of raised ICP

Tumour


Abscess


Encephalitis


Hydrocephalus


Idiopathic intracranial hypertension

Optic Nerve Tract Lesions?

Cranial Nerve 3 (Occulomotor Lesion) causes?


PCA aneurysm


Raised ICP


GCA


DM


HTN

What muscles does the occulomotor nerve supply?

Superior Rectus


Inferior Rectus


Medial Rectus



Inferior Oblique


Sphincter Pupillae


Levator Palpebrae Superioris

What do you see in a patient with CN3 palsy?

Eye is DOWN and OUT 


DILATED PUPILS 


Ptosis

Eye is DOWN and OUT


DILATED PUPILS


Ptosis

Most common symptoms of a brainstem infarct?

Lateral Medullary Syndrome


= Occlusions of one vertebral artery / posterior inferior cerebellar artery


= Vertigo / Vomiting/ Dysphagia / Nystagmus / Ipsilateral ataxia / Ipsilateral Horner's Syndrome

What muscle does CN4 supply?

TROCHLEAR NERVE


SO4? = Superior Oblique

Clinical Features of CN4 palsy?

Diplopia on looking down and in 


Head tilting compensation (OCULAR TORTICOLLIS) 

Diplopia on looking down and in


Head tilting compensation (OCULAR TORTICOLLIS)

CN6 (Abducens) Which Muscle?

Lateral Recturs


Eye cannot be abducted beyond the midline


Horizontal diplopia on looking outwards

CN 5 - What Nerve? What lost first? What does it supply?

Trigeminal Nerve


3 Branches = Opthalmic/Maxillary/Mandibular


Supplies sensation to these three areas


CORNEAL reflex is lost first



Motor = Travels with Mandibular - supplies muscles of mastication = JAW deviates TOWARDS the side of the lesion


Causes of CN5 palsy

Sensory? = Trigeminal Neuralgia / Herpes


Motor? (Rare) = Nasopharyngeal Carcinoma / Acoustic Neuroma

What is CN7?

Facial Nerve


Supplies muscles of expression in the face


Two major branches


1) Chorda tympani


2) Stapedius

What causes a CN7 lesion?

Fracture affecting the PETROUS bone

What happens in an LMN CN7 lesion

Ipsilateral weakness of the facial expression muscles


commonest = BELLS PALSY

What is Bell's Palsy

Sudden onset unilateral facial weakness


Ipsilateral numbness/pain around the ear


Hypersensitive to sounds



Drooling


Frontalis weakness


Eyes can't close

Investigation's of Bell's Palsy

ESR


Glucose


Increase in Borrelia Antibodies in Lyme Disease


MRI

Complications of Bell's Palsy

Synkinesis


Crocodile Tears

Management of Bell's Palsy?

Prednisolone


Protect Eyes


= Dark glasses / Lateral Tarsorrhaphy / Artificial Tears

Causes of Bell's Palsy

HSV


HIV


EBV


CMV


Sarcoidosis


Lyme Disease

Other causes of LMN lesions?

Polio


Otitis Media


Acoustic Neuroma


Malignant parotid tumours


Herpes Zoster = RAMSAY HUNT SYNDROME

What is Ramsay Hunt Syndrome?

LATENT VARICELLA ZOSTER VIRUS reactivates in the geniculate ganglion



= Painful vesicular rash on auditory canal


= Loss of taste in anterior 2/3rd of tongue



Rx = ACICLOVIR / PREDNISOLONE

UMN Lesion of the facial nerve?

Weakness in the lower part of the face


Upper facial muscles are SPARED (Can still lift eyebrows)


Cause = Stroke / Tumour

CN8 palsy- clinical features?

Vestibulocochlear nerve



Vetibular = Equilibrium


Cochlear = Hearing



Sensorineural Deafness and tinnitus


Vertigo (Illusion of movement)


Vomiting


Nysatgmus (Pendular = poor visual fixation - Jerk Horizontal = Middle Ear - Jerk Vertical = Brain stem/Cerebellum)


Ataxia C

Causes of CN8 Palsy

ACOUSTIC NEUROMA


Paget's


Gentamicin


Meniere's disease

CN9-12?

Glossopharyngeal


Vagus


Accessory


Hypoglossal



All usually affected together (Bulbar palsy)

CN9-11 lesion causes?

Trauma / Jugular Foramen Lesion

Groups of CN's affected?

CN8 ---> 5/6/9/10 = Cerebellopontine angle tumours (Acoustic Neuroma)



CN3/4/6 = Stroke/MS



CN3/4/5(a)/6 = Cavernous Sinus thrombosis



CN9/10/11 = Jugular Foramen Lesion

5 clinical features of a space occupying lesion?

1) RAISED ICP


- Worse on walking/lying/bending forward/coughing


- Vomiting / Papilloedema


- As tumour grows = downward displacement of brain + pressure on stem = drowsiness/respiratory depression/coma



2) SEIZURES


3) EVOLVING FOCAL NEUROLOGY


6th nerve / 3rd nerve palsy


4) SUBTLE PERSONALITY CHANGE


Irritable/Apathy/Socially inappropriate behaviourC

Causes of a space occupying lesion?

Tumour


Abscess


Aneurysms


Chronic subdural haematoma


Tuberculos

5 primary brain tumours

Astrocytoma


Glioblastoma Multiforme


Oligodenroglioma


Ependymoma


Meningioma

Investigations for an SOL?

CT/MRI



NO NO NO LP = Cerebellar tonsils will hermiate through the foramen magnum = death

What is the management for an SOL?

1) Excision + Carmustine wafers


2) Hydrocephalus? Ventriculo-peritoneal shunt


3) Glioblastoma? TEMOZOLOMIDE


4) Cerebral Oedema? Dexamethasone / Mannitol

Clinical Features of a frontal lobe SOL?

Hemiparesis


Personality Change


Grasp Reflex


Brocca's Dysphasia


Unilateral anosmia

Clinical Features of a PARIETAL lobe SOL?

Hemisensory loss


Decreases 2 point discrimination


Astereognosis


Sensory inattention


Dysphasia

Clinical Features of a TEMPORAL lobe SOL?

Dysphasia


Contralateral homonymous hemianopia


Amnesia

Clinical Features of an OCCIPITAL lobe defect?

Contralateral visual field defects


Palinopsia


Polyopia

Symptoms of a Cerebellopontine angle lesion?

Acoustic Neruoma / Vestibular Schwannoma


Ipsilateral deafness


Nystagmus


Decreased corneal reflex


Facial weakness


IPSILATERAL cerebellar signs


Papilloedema


6th nerve palsy

What is the classic symptom of a mid-brain infarction (pineal tumour)

Failure of up or down gaze

3 ways in which micro-organisms can reach the meninges?

Ears


Nasopharynx


Bloodstream

5 causes of meningitis

NHS



Neisseria Meningitides


Haemophilus Influenzae


Streptococcus Pneumoniae


Listeria monocytogenes


Cryptococcus


TB (If immunocompromised)

Clinical Features of Meningitis

Initially = Headache/ Leg Pains/ Cold Hands & Feet


Later=


MENINGISM = Neck stiffness / Photophobia / Kernig's Sign


Decreased conscious level / coma / seizures/ focal CNS signs

What would you suspect if you saw a petechial rash that is NON-BLANCHING on a patient with meningitis?

MENINGOCOCCAL SEPTICAEMIA

Complications of Meningitis

Venous Sinus Thrombosis


Severe cerebral oedema


Cerebral abscess

Causes of VIRAL Meningitis

Coxsackie A


Coxsacke B


Echovirus


HSV2



Rx = Aciclovir - usually self limiting

Management of Meningitis?

At GP before hospital = BEN PEN


At hospital


<55 years old = IV CEFOTAXIME


>55 years old = IV CEFOTAXIME + AMPICILLIN (for Listeria)

Prophylaxis for meningitis?

Rifampicin

Investigations for Meningitis?

HEAD CT SCAN


U&E/FBC/LFT/ Blood Culture


If the patient is immunocompromised with meningitis, what stains do you use?

Auramine stain = TB


India ink stain = Cryptococcus

What would you see in the CSF of a patient with meningitis?

1) Bacterial? Low glucose/ Neutrophilia


2) TB = Low glucose / Lymphocytosis


3) Viral = High protein/ Lymphocytosis



4) SAH = High RBC

What is encephalitis?

Inflammation of the brain parenchyma

Symptoms of encephalitis?

Odd behaviour


Headache/Fever


Reduced consciousness


Focal neurological deficit / Seizure


Coma

What is the difference between encephalopathy and encephalitis?

Encephalopathy = NO PRODROME


Encephalitis = Prodome (Fever/Rash/Lymphadenopathy)

Causes of Encephalopathy

Hypoglycaemia


Hepatic encephalopathy


DKA


SLE

Viral (most common) causes of encephalitis

HSV1


HSV2


CMV


EBV


HIV


Varicella-Zoster Virus



ALSO = Japanese B Encephalitis / West Nile VirusN

Non viral causes of encephalitis

Any bacterial meningitis


TB


Malaria


Listeria


Lyme disease


Schistosomiasis


Legionella I

Investigations for Encephalitis?

1) Bloods - Blood Culture / Serum for viral PCR /Malaria FIlm


2) Contrast enhanced CT


3) LP


4) EEG

Management for Encephalitis?

IV ACICLOVIR

What causes shingles?

After an infection with varicella zoster (chicken pox) - the virus remains dormant in:


1) DORSAL ROOT GANGLION


2) CRANIAL NERVE GANGLIA



Reactivation of the infection = Shingles

Clinical Features of Shingles

Pain + Tingling in dermatomal distribution


RASH


= Lower thoracic region / Opthalmic division of the trigeminal


Fever


Malaise M

Management of shingles?

IV ACICLOVIR

Compleciation of Shingles and Management?

Post-Herpetic Neuralgia



Amitriptyline + Carbamazepine


(or topical lidocaine patches / gabapentine)



Last resort = Ganglion ablation