Neurology Flashcards

1
Q

Symptoms of idiopathic intracranial hypertension

A

The symptoms include:

Headache behind the eyes
Ringing in the ears
Blurred vision
Double vision
Short temporary episodes of blindness
Nausea and vomiting
Dizziness
Papilledema (swelling of the optic disc in the eyeball) (fundoscopy)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Symptoms of raised intracranial pressure (red flag)

A
  • headaches worse in morning and upon bending over
  • headaches improve after vomiting or lying down
  • May be associated with neurological deficits due to compression of cranial structures by a space-occupying lesion, such as a tumour or haemorrhage.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Migraine definition

A
  • headache lastin 4-72hrs
    at least 2 of following characteristics:
  • unilateral location
  • pulsating quality
  • ## moderate or severe pain intensity
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Chronic migraines definition

A

Headache > or on 15 days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Acute treatments for migraines

A
  • ## painkillers i.e paracetamol NSAIDs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Preventative treatments for migraines

A
  • Amitryptiline
  • Propanolol

Can also use botox for chronic migraines
New treatment: fremanuzumab

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Symptoms of cluster headaches

A
  • recurrent attacks of sudden unilateral periorbital pain
  • associated with watery eyes, runny nose (rhinorrhoea), blood shot eye, lacrimation, miosis, ptosis, lid swelling, and facial flushing
  • last 15 minutes to 3 hours, occur once or twice a day, over a period of 4-12 weeks, and are followed by a pain-free period of months before the next cluster begins
  • pts tend to bang head in first attack as it relieves pain slightly
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Management of cluster headaches

A

Acute management:
- high flow oxygen with 100% via non-breathable mask (contraindication COPD) with subcutaneous or nasal Triptan (CI: ischaemic heart disease)
- steroids can also be used

Preventative/avoid triggers:
- prophylaxis with Verapamil (calcium channel blocker)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Definition of cluster headaches

A

1 in 500 people
one sided
cranial autonomic features (tears, runny nose, red eye, drooping eyelid)
30-120 mins (bit shorter than migraines)
pt can be really agitated unlike a migraine
- need a scan - 10% people may have abnormality in pituitary gland

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Symptoms of migraines:

A
  • a unilateral throbbing headache preceded by an aura, such as visual (eg. lines, zigzags) or sensory (paraesthesia spreading from fingers to face) symptoms
  • headache may last 4-72 hours
  • associated with photofobia or phonophobia
  • May be identifible triggers
  • vomiting common
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Definition of myasthenia gravis

A

autoimmune
progressive muscle weakness
nictitonic acetylcholine receptor antibodies produced by immune system, blocks post synaptic receptors, acetylcholine can’t bind, unable to contract/communication with muscles

linked to thymus gland tumours (thymomas)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Symptoms of myasthenia gravis

A

weakness of proximal limbs, facial muscles, eye lid muscles
worse in evening/end of day, better in morning
worsens with activity, better with rest

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Investigations for myasthenia gravis

A

Bloods:
- serum acetylcholine receptor antibody
- muscle-specific tyrosine kinase antibodies (should be ordered if the acetylcholine receptor antibody is negative or equivocal)

  • CT of the chest look for tumours of thymus
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Give 3 examples of trinucleotide repeat disorders which result in neurological conditions

A

huntington’s (CAG repeat in HTT gene, chr 4)
Fragile X (CGG repeat in FMR1 gene on chr X)
Myotonic dystrophy (CTG repeat in DMPK gene on Chr 19).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Clinical features of small fibre peripheral neuropathy

A

burning pain
allodynia (non-painful stimuli experienced as pain)
hyperalgesia (painful stimuli experienced as severe pain)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Causes of motor-predominant peripheral neuropathy

A

gullain barre syndrome
hereditory motor neuropathies
acute intermittent porphyria
lead poisoning
paraneoplastic syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

definition of motor peripheral neuropathy

A

damage to peripheral nerves responsible for motor functions e.g foot drop

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Causes of cerebellar syndrome

A

vascular: stroke
Infective: Lyme disease
Inflammatory: Multiple scleorisis
Traumatic: traum to posterior fossa
Metabolic: alcoholism
Iatrogenix: phenytoin, carbamazapine
tumours
vitamine E deficiecny

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is subdural haemorrhage

A

caused by collection of venous blood accumulating in potential space between dura mate and arachnoid mater (subdural space)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Aetiology of subdural haemorrhage

A

elderly pts following minor trauma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Risk factors for subdural haemorrhage

A

advancing age >65
Bleeding disorders or anticoagulation therapy
chronic alcohol use
recent trauma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Presentation of subdural haemorrhage

A

typically sub acute (within 3 days to 3 weeks) chronic (>3 weeks)
headache, nausea, vomiting, confusion, diminished eye/verbal/motor response
may be focal signs in haematoma site

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

dx of subdural haemorrhage

A

CT scan

-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the ROSIER screening?

A

scoring system used in acute settings such as A&E to recognise stroke

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
What is the definition of vertigo?
Hallucination of movement of oneself or one's environment movement often rotatory e.g floor is tilting
26
Causes of vertigo
benign positional paroxysmal vertigo (BPPV) acute labyrinthitis Meiniere's disease acoustic neuroma Ramsay hunt Ototoxicity
27
features of benign positional paroxysmal vertigo (BPPV)
presence of debris in semicircular canals of ears cause vertigo upon head movements Hallpike manourve is diagnostic epley manourves treat by clearing debris
28
Features of acute labyrinthitis
inflammation of vestibular nerve causing acute severe vertigo, may be associated with vomiting hearing loss, and tinitus associated with recent illness or vascular lesion often resolves over a month, treatment is conservative
29
Meniere's disease features
endolymphatic system pressures increase causing recurrent episodes of vertigo, sensorineural hearing loss, tinnitus and feeling or aural fullness tx: antihistamines and bed rest
30
features of acoustic neuroma
/
31
Ramsey Hunt syndrome features
herpetic infection of facial nerve causing facial nerve palsy, with or without vertigo, tinnitus and hearing loss Tx: aciclovir and prenisalone
32
Ototoxicity features
Aminoglycoside abx (gentamicin, vancomycin) and loop diuretics (furesomide)
33
What type of brainstem stroke can cause locked in syndrome?
Acute basilar artery infarct
34
Which is the first line of treatment in cases of optic neuritis?
Intravenous methylprednisolone
35
What is the management of a haemorrhagic stroke following ABCDE assessment?
Obtain neurosurgical opinion regarding surgical intervention (e.g decompressive hemicraniectomy)
36
What are the features of lateral pontine syndrome?
Lateral pontine syndrome (anterior inferior cerebellar artery): contralateral loss of pain/temperature on the body , ipsilateral nystagmus & vertigo & nausea/vomiting ipsilateral facial paralysis , ipsilateral deafness and tinnitus, ipsilateral ataxia ipsilateral impaired facial sensation
37
Features of posterior circulation infarct?
cerebellar dysfunction OR conjugate eye movement disorder OR Bilateral motor/sensory deficit OR ipsilateral cranial nerve palsy with contralateral motor/sensory deficit OR cortical blindness/isolated hemianopia
38
What is Foville's syndrome?
/
39
What is Horner's syndrome
interruption of the sympathetic nervous supply to the eye
40
Causes of Horner's syndrome
pancoast tumour (affecting sympathetic nervous supply) Stroke Carotid artery dissection (red flag: neck pain)
41
Clinical presentation of Wallenburg syndrome
DANVAH Dysphagia ipsilateral Ataxia ipsilateral Nystagmus Vertigo Anaethesia (ipsilateral facial numbness and contralateral pain loss on the body) ipsilateral Horner's syndrome
42
What causes Wallenburg syndrome
infarction of posterior inferior cerebellar artery (PICA)
43
Features of cerebellar syndrome
DANISH dysdiadochokinesia (inability to perform rapid alternating hand movements) Ataxia (broad based unsteady gait) Nystagmus (involuntary eye movements) Intention tremor (finger nose test) Slurred speech hypotonia
44
Causes of cerebellar syndrome
VITAMIN C vascular: stroke Infective: Lyme disease Inflammatory: multiple scleorisis Traumatic: trauma to posterior fossa Metabolic: alcoholism Iatrogenic: phenytoin and carbamezepine Neoplastic: primary tumours (cerebellopontine angle tumour) Congenital: Friedrich's ataxia
45
A 70 year old male patient presents to the emergency department with sudden onset unsteadiness. His wife reports that his speech is slurred and he appears to be walking as if drunk. He has a past medical history of hypertension and hypercholesterolaemia. On physical examination there is ataxia, right-sided intention tremor, dysarthria and nystagmus. Which of the following is the most appropriate urgent investigation?
CT head most appropiate in pts with suspected stoke
46
A patient presents with unsteadiness on their feet. The doctor performs a test whereby the patient is asked to stand up with their eyes open, and then they are asked to close their eyes. The patient is stable with their eyes open, however upon closing the eyes, they become unsteady. Which of the following is the most appropriate conclusion?
pt is Rhomberg's positive and has sensory ataxia its sensory because it happens when eyes are closed
47
Clinical features of Herpes Zoster ophthalmicus
painful red eye, fever, malaise and headache precede typical erythematous vesicular rash over trigeminal division of opthalmic nerve
48
Treatment of Herpes Zoster ophthalmicus
Oral aciclovir with topical steroids.
49
What is encephalitis
infalmmation of encephalon or brain parenchyma
50
Clinical features of encephalitis
altered mental state fever flu like symptoms early seizures
51
Cause of encephalitis
herpes simplex virus type 1
52
What causes encephalopathy
hypoglycaemia hepatic encephalopathy DKA drug induced SLE
53
Investigations for encephalitis
suspected in any pt with sudden onset behavioural change, new seizures and unexplained acute headache with meningism blood tests, blood cultures, viral PCR CSF malaria blood forms
54
treatment of encephalitis
broad specturm abx with 2g IV ceftriaxone BD and 10mg/kg aciclovir TDS for 2 weeks
55
side effects of aciclovir
generalised fatigue/malaise GI disturbance photosensitivity and urticarial rash acute renal failure haem abnormalities hepatitis neurological reactions
56
What are focal seizures with impairment of consciousness (complex focal seziures)?
pts lose consciousness either after an aura or at seizure onset most commonly originate from temporal lobe post-ictal sx common e.g confusion in temporal lobe seizures.
57
What are simple focal seizures?
without impairment of consciousness pts don't lose consciousness, only experience focal sx post-itcal sx don't occur
58
What are secondary generalised focal seizures
focal seizure --> tonic-clonic
59
Features of temporal-lobe specific focal sezirue
automatisms (lip-smacking, deje vu, jamais vu, emotional disturbance 'sudden terror', olfactory, gustatory or auditory hallucinations
60
Features of frontal-lobe specific focal sezirue
motor features e.g jacksonian features, dysphasia, Todd's palsy
61
Features of parietal-lobe specific focal sezirue
sensory symptoms; tingling and numbness, motor sx: spread of electrical activity to pre-central gyrus in frontal lobe
62
Features of occipital-lobe specific focal sezirue
visual symptoms such as spots and lines in visual field
63
What are absent seizures
pts often children pause briefly, for less than 10 seconds, then carry on where they left off. Tx: sodium valporate (SE: weight gain, hair loss, oedema, ataxis, tremor, tetraogenicity) or ethosuximide 1st line AVOID carbamazepine as makes seizures worse
64
What are tonic clonic seizures
pts lose consciouness limbs stiffen and then start jerking post-ictal confusion TX: sodium valporate or lamotrigine 1st line
65
What are myoclonic seizure
sudden jerk of limb, trunk or face. Tx: sodium valporate 1st line unless pt is woman of child bearing age then it's levetiracetam or topiramate. AVOID carbamazapine
66
What are atonic seizures
sudden loss of muscle tone, causing pt to fall whilst retaining consciousness Tx: sodium valporate or lamotrigine
67
What are complications of epilepsy
status eplicticus (treat with IV lorazepam/buccal midazolam, then phenytoin depression suicide sudden unexpected death in epilepsy
68
mx for focal seizures
carbamazepine, gabapentin and phenytoin
69
What is giant cell arteritis
arteries on side of head become inflammed
70
Presentation of giant cell arteritis
temporal headache jaw claudication (pain on chewing food) amaurosis fugax (like dark curtain descending vertically in vision) thickened, tender temporal artery on examination scalp tenderness
71
complications of giant cell arteritis
stroke permenant monocular blindness
72
investigations for giant cell arteritis
ESR, FBC, LFTS definitive investigation: temporal artery biopsy
73
mx for giant cell arteritis
high dose steroid: 60mg OD prednisolone
74
What is cauda equina syndrome
compression of cauda equina L1
75
Cause of cauda equina syndrome
lumbar disc herniation at L4/5 and L5/s1
76
Clinical features of cauda equina syndrome
lower back pain bilateral radicular pain saddle anaethesia bladder and bowel disturbance
77
Mx of cauda equina syndrome
urgent WHOLE spine MRI surgical decompression in pts where malignancy seen or suspicion high: 16mg OD dexamethasone with PPI cover
78
What is brown-sequard syndrome
anatomical dsiruption of nerve fibre tracts in one half of spinal cord
79
Clinical features of brown-sequard syndrome
disruption of descending lateral corticospinal tracts, ascending dorsal column and ascending spinothalamic tracts ispilateral hemiplegia ipsilateral loss of proprioception and vibration contralateral loss of pain and temp sensation
80
Causes of brown-sequard syndrome
cord trauma neoplasma disk herniation demyelination infective/inflammatory lesions epidural haematomas
81
Mx of brown-sequard syndrome
surgery or medical
82
What is Guillain- Barre syndrome
ascending inflammatory demyelinating polyneuropathy
83
Clincial features of Guillain- Barre syndrome
progressive ascending symmetrical limb weakness, starts from feet and moves up reduced reflexes and loss of sensation 4 WEEKS AFTER INFECTION OF GASTRITIS/DIARRHOEA/FOOD POISONING
84
mx of Guillain- Barre syndrome
IV immunoglobulins Intubation/ventiliation IF RESP FAILURE FVC NEEDS TO BE MONITORED
85
Causes of Guillain-Barre Syndrome
Campylobacter jejuni infection
86
what cranial nerve lesion is seen in left sided Bell's palsy
Left 7th cranial nerve LMN lesion
87
mx of TIA
300mg aspirin review in 24hrs
88
1st line treatment of optic neuritis
IV methlyprednisolone
89
1st line imaging investigation in acute stroke
non-contrast CT head why? exclude haemorrhage
90
secondary stroke prevention
HALTSS hypertension: anti-tensive therapy Antiplatlet therapy: clopidogrel 75mg OD lipid lowering drugs: 20-80mg ON atorvastatin smoking cessation diabetes managed appropiately surgey
91
What type of brainstem stroke can cause locked in syndrome?
acute basilar artery infarct
92
cardinal signs of middle cerebral artery stroke
contralateral hemiplegia contralateral homonymous hemianopia dysphasia
93
how do lesions in medulla present
cranial nerve IX, X, XI, XII palsies
94
What are the features of a total anterior circulation infarct according to the bamford classification?
contralateral hemiplagia or haemparesis AND contralateral homonymous hemianopia AND higher cerebral dysfunction (aphasia, neglect)
95
What are the features of a posterior circulation infarct according to the bamford classification?
Cerebellar dysfunction, OR Conjugate eye movement disorder, OR Bilateral motor/sensory deficit, OR Ipsilateral cranial nerve palsy with contralateral motor/sensory deficit, OR Cortical blindness/isolated hemianopia.
96
What is the Oxford-Bamford criteria for a total anterior circulation stroke?
All three of 1) Unilateral weakness and/or sensory deficit in the face, arm and leg 2) Homonymous hemianopia 3) Higher cerebral dysfunction (dysphasia, visuospatial disorder)
97
To be eligible for thrombolysis, which time window must patients with ischaemic stroke present in?
less than 4.5 hrs sx onset
98
What are the features of a partial anterior circulation infarct according to the bamford classification?
A partial anterior circulation infarct (PACI) is defined by: 2 of the following: Contralateral hemiplegia or hemiparesis, AND Contralateral homonymous hemianopia, AND Higher cerebral dysfunction (e.g. aphasia, neglect) OR Higher cerebral dysfunction alone.
99
Which stroke syndrome affects the medulla?
Lateral medullary syndrome (posterior inferior cerebellar artery)
100
If speech is affected, which hemisphere is affected?
Dominant hemisphere strokes (Left side of the brain for most people) can cause dysphasia or aphasia.
101
Which stroke syndrome affects the Pons?
Lateral pontine syndrome (anterior inferior cerebellar artery)
102
What symptoms do MCA lesions produce?
Middle cerebral artery infarcts affect the contralateral arm, leg and face.
103
4 causes of painless monocular visual loss
anterior ischaemia optic neuritis amaourosis fugaz vitreous hamorrhage retinal detachment
104
Risk factors for haemorrhagic stroke
age, male, haemophilia, cerebral amyloid angiopathy/hypertension, anti-coagulation, sympathomimetic drugs (cocaine, amphetamines)
105
mx of Myasthenia gravis
acute - steroids long term - acetylcholinesterase inhibitors (pyridostigmine or neostigmine)
106
mx of myasthenic crisis
Ventiliation (resp failure) IV immunoglobulins
107
pathophysiology of guillain-barre syndrome
b cells produce antibodies to infection antigen (campylobacter jejuni) antibodies also match receptors of neurons antibodies produced attack nerves (motor)
108
pathophysiology of multiple sclerosis
demeylenation of CNS neurons immune system attacks neurones - struggle to commincate --> results in sensory, motor + cognitive problems
109
4 types of multiple sclerosis
relapsing - remitting secondary progressive primary progressive progressive relapsing
110
acute progressive weakness spasitic paraparesis, brisk reflexes patchy sensory disturbances white matter plaques on brain MRI optic neuritis oligoclonal bands in CSF periventricular plaques presentation of what neurological disease?
Multiple sclerosis
111
mx of acute attack Multiple sclerosis
IV methyl prednisolone (1g) if doesnt work - plasma exchange
112
chronic mx of Multiple sclerosis
injectable beta interferon
113
investigations to support dx of Multiple sclerosis
CSF MRI