neuro Flashcards

1
Q

Px presents with unilateral facial pain limited to the mandibular region, brought on by brushing their teeth , given the likely diagnosis what would be the first line treatment?
Would disease would you consider investigating for?

A

Dx: trigeminal neuralgia

Tx: carbamazepine

Associated disease: MS

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2
Q

35 year old women presents to A+E with a sudden onset headache, PMH of smoking.
What is the most likely underlying pathology?
What is the first line Ix, and what would you see?
How would you Tx?

A

Pathology: SAH, rupture of berry aneurysms

Ix: CT head, ‘white star’ - blood in cisterns

Tx: intracranial aneurysm - coiling
IV fluids
nimodipine - prevent vasospasm (for 21 days)

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3
Q

38 year old male smoker presents with intense left sided pain around 1 eye, he gets the pain for 1 hour every day for the last 2 weeks, on examination his left eye is red and watery.
What is the most likely Dx?
How would you manage the headache?
Would would you give to prevent the headache?

A

Dx: Cluster headache

Mx: 100% high flow oxygen for 15 mins + SC 6mg sumatriptan

Px: verapamil (CCB) or prednisolone to break the cycle

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4
Q

A 60 year old male presents to A+E with a headache, neck stiffness and a 38.1 C fever, given the suspected Dx..
What special tests could you do?

WHat is the most likely causative organism?

What Ix would you like to carry out?

The LP is cloudy and has a low glucose and high protein - what Mx would you offer?

What prophylaxis is any should be given to contacts?

A

special tests: Kernig’s and Brudzinki’s

organism: Neisseria meningitidis (or Strep. pneumoniae)

Ix: LP (+PCR) + blood culture + bloods
CSF:
Bacterial - cloudy, low glucose, high protein, high polymorphs
Viral - clear/cloudy, normal ish glucose (60-80%), normal/riased protein
TB: Slightly cloudy/’fibrin web’, low glucose, high protein
Fungal: cloudy, low glucose, high protein

Bacterial more common than fungal so suspect that first, can be differentiated with WCC - B: 10-5000 polymorphs, F: 20-200 lymphocytes

Mx: IV cefotaxime

Contact prophylaxis: Ciprofloxacin

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5
Q

A 2 year old presents to GP with fever, drowsiness, her parents tell you she does not want to eat which is unusual for her and she won’t stop crying.
What is a DDx?
How would you Ix?
What is the most likely causative organism?
How would you Tx?

A

DDx: meningitis, encephalitis

Ix: LP - encephalitis would show increased lymphocytes

organism: HSV 1 (or 2)

Mx: IV acyclovir

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6
Q
A 51 year old man presents to his GP with a single seizure and a constant headache, he reports its worst on walking especially hills, constantly there, severity 7/10, not relieved by paracetamol. 
What DDx do you want to rule out? 
How would you Ix? 
What is the most common type? 
how would you Mx?
A

Dx: Space occupying lesion / brain tumour

Ix: MRI head

type: 1. brain metastases, 2. glioma , oligodendroglioma, pituitary tumour, acoustic neuroma

Mx: surgical resection + chemo + radio (or palliative)

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7
Q

32 year old pregnant women presents to the GP with 1 day Hx of right sided facial droop, dry eyes and right sided ear pain and reports being extremely sensitive to sound.
What is the most likely Dx?
What Tx would you offer?

A

Dx: Bell’s palsy

Mx: 10 days prednisolone within 72 hours of onset and eye lubrication

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8
Q
A 24 year old female present to GP with a 2 day Hx of weakness in her legs up to her knee and she says this morning she began to lose sensation in her fingers on both sides. She tells you 2 weeks ago she had D+V. On examination you cannot elicit an ankle reflex. 
What is the most likely Dx? 
What criteria could you use to Dx? 
Would Ix could help you Dx?
how would you manage her? 
What is the prognosis?
A

Dx: Guillian-Barre (following gastroenteritis)

Criteria: Brighton criteria

Ix: nerve conduction studies would be abnormal, LP would show CSF with high protein

Mx: IV immunoglobulins + plasma exchange
Give VTE prophylaxis

Px: 80% fully recover

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9
Q

21 year old male presents to GP with 3 day Hx of R-sided ear pain and a rash around the ear, he also thinks his speech sounds slurred today. O/E you note he has R-sided facial weakness.
What is you most likely Dx?
What Mx do you offer?
What is the cause of this condition?

A

Dx: Ramsey-Hunt syndrome

Mx: oral acyclovir

Cx: reactivation of VZV

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10
Q

29 year old female comes to GP with a 2 days Hx of a rash on her arm that looks like a bulls eye, she also reports her joints feel stiffer than usual as she struggled with her morning yoga today. She regularly walks in the local woods.
What Dx are you thinking of? What other signs could be present?
how would you manage ?
What reaction could occur following Tx?

A

Dx: Lyme disease
could have fever
Cardiac: heart block, myocarditis
Neuro: facial palsy, meningitis

Mx: ABx

early: doxycycline
late: ceftriaxone

Reaction: Jarisch-Herxheimer reaction (more common when Tx syphilis)
fever, rash, tachycardia after first ABx

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11
Q

A 6 year old boy is brought to the GP as he is complaining of blurred vision and he has started to squint. On examination he has >8 coffe-coloured 5mm patches on his skin over his body and freckles in his groin region.
What Dx are you considering?
What Mx do you offer?

A
Dx: Neurofibromatosis type 1 (chromosome 17 AD)
Mutation in neurofibromin 
other CF: 
Café-au-lait spots (>= 6, 15 mm in diameter)
Axillary/groin freckles
Peripheral neurofibromas
Iris hamatomas (Lisch nodules) in > 90%
Scoliosis
Pheochromocytomas

Mx:
Monitoring to prevent complications
Chemo to shrink the optic nerve neuroma

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12
Q

A 17 year old boy presents to GP with gradual hearing loss and ringing in both ears and reports he’s more unsteady on his feet than normal. For the past week he thinks his face looks strange.
O/E you note weakness of the facial muscles bilaterally. You are unable to elicit the corneal reflex.
What Dx are you thinking?
how would you investigate?
how would you manage?

A

Dx: type 2 neurofibromatosis (C22, AD) affects schwann cells

Ix: MRI at cerebellopontine angle - bilateral vestibular schwannomas / acoustic neuromas

Mx: can be surgically removed if symptomatic

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13
Q

Joanna is a 24-year-old female who presents to the emergency department with an abrupt 2-hour onset of a painful and red skin rash extending across her trunk, face, and limbs. She has never had this skin rash before and has not recently used any new skin products. Her past medical history includes epilepsy, and a viral upper respiratory infection a couple of weeks ago. Her medications include lamotrigine which was started 3 weeks ago.

On examination, Joanna’s blood pressure is 120/80mmHg, pulse 90/min, respiratory rate 18/min, and she is afebrile. There is diffuse skin erythema, macules, and flaccid blisters across the majority of her body (except the palms and soles of the feet). There are also notable ulcers on her lips and genitalia.

What is the most likely Dx?

What is the most important immediate step in management?

A

Stevens-Johnson syndrome (SJS), rare SE of lamotrigine.
SJS usually develops up to two months after starting an anti-convulsant. Usually there is a prodromal illness which resembles a viral upper respiratory tract infection or ‘flu-like illness’. After this, there is a rapid onset of a painful red skin rash which starts on the trunks and extends abruptly onto the face and limbs. Interestingly, this rash rarely affects the scalp, palms or soles.

cease all meds and give IV fluids

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14
Q

What malformation is syringomyelia associated with?

A

Arnold-Chiari malformation (lower part of the brain pushes down into the spinal cord)

Syringomyelia:
In Syringomyelia a fluid filled cyst forms in spinal cord and expands over time. This causes slowly progressive neurological symptoms as seen in this patient.
- ‘cape’ like loss of sensation (don’t realise they burn themselves)
- weakness of lower limbs

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15
Q

What is vitamin deficiency results in wernicke’s ?

What is the triad most commonly seen in wernicke’s encephalopathy?

A

thiamine / B1

  1. ophthalmoplegia / nystagmus
  2. ataxia
  3. confusion
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16
Q

A 24-year-old lady presents to her GP where she proceeds to have a convulsive episode involving her whole body in the waiting room. During the episode, she is not able to speak but can make eye contact when her name is called. After the episode she quickly returns to normal and is able to remember everything that happened during the episode. Her past medical history includes post-traumatic stress disorder and alcohol overuse.

What is the most likely diagnosis?

A

psychogenic non-epileptic seizure

Can remain aware in focal seizures but would not usually involve whole body

17
Q

A nurse calls you do a war where a patient is in status epilepticus. What can you give them to terminate the seizure?

A

4mg lorazepam IV, repeat after 10 mins if not resolved

Persisting - IV phenobarbital / phenytoin (requires cardiac monitoring)

18
Q

A 54 year-old female presents with a loss of dexterity in both hands. She has been struggling to type at work and use her mobile phone. Her symptoms have been deteriorating gradually over the preceding months.

A

degenerative cervical myelopathy - loss of fine motor in both upper limbs (loss of dexterity)

19
Q

What symptoms would be suggestive of a frontal lobe lesion?

A

it may cause difficulty with controlling emotions and behaviour, lack of inhibition, speaking, communication skills and language production, executive functions (making decisions, solving problems, planning and organising) and social cognition, impulse control and sexual behaviour.

20
Q

What symptoms would be suggestive of a parietal lobe lesion?

A
  • sensory inattention
  • apraxias
  • astereognosis (tactile agnosia)
  • inferior homonymous quadrantanopia
  • Gerstmann’s syndrome (lesion of dominant parietal): alexia, acalculia, finger agnosia and right-left disorientation
21
Q

What symptoms would be suggestive of an occipital lobe lesion?

A

eye signs:
homonymous hemianopia (with macula sparing)
cortical blindness
visual agnosia

22
Q

what symptoms would be suggestive of a cerebellar lesion?

A

midline lesions: gait and truncal ataxia

hemisphere lesions: intention tremor, past pointing, dysdiadokinesis, nystagmus

23
Q

What symptoms are suggestive of a temporal lobe lesion?

A

Wernicke’s aphasia: this area ‘forms’ the speech before ‘sending it’ to Brocas area. Lesions result in word substituion, neologisms but speech remains fluent
superior homonymous quadrantanopia
auditory agnosia
prosopagnosia (difficulty recognising faces)

24
Q

A 34 year old women presents to GP with painful eye movements which get worst when she is in the bath and sometimes result in loss of vision.
What other CF would you want to ask about?

A

CFs:
Charcots triad:
- Dysarthria - difficult, unclear speech
- Intention tremor (+ motor signs: muscle weakness typically in lower limbs)
- Nystagmus (visual symptoms - optic neuritis)

  • Uhthoff’s phenomenon: worst vision on increased temp
  • Sensory: trigeminal neuralgia, pins and needles, Lhertmitte’s sign (electric shock sensation down spine on neck flexion)
  • cerebellar signs: ataxia
  • Fatigue, incontinence, sexual and bowel dysfunction, intellectual deterioration.
25
Q

You suspect a patient has MS, what Ix would you carry out?
What criteria would you use?
How would you manage them?

A

Flare MRI - white plaques
LP - oligoclonal bands, antibodies in CSF not serum

Macdonald criteria: 
- Time and space
- no alternative 
- >= typical relapse 
= symps >48 hours and progressive. 

Mx:
Acute: high dose IV methylprednisolone
Disease modifying: beta-interferon , dimethyl-fumarate (tablet) and ocrelizumab (infusion)

26
Q

A 65 year old man presents to the GP complaining of food getting stuck when he is trying to swallow more often and getting an achy jaw when eating. This has been going on for a month.

What is the most likely Dx?
What is the most likely Cx?
How would you diagnose?
How would you Mx?

A

Dx: myasthenia gravis

Cx: Autoimmune (80-90%) or thymoma (10-20%)

Ix: serum AchR antibodies
or CT/MRI of thymus

Mx: long-term - pyridostigmine (ACh-esterase inhibitors) + immunosuppression (prednisolone)
Thymectomy

Crisis: acute worsening of symptoms
Mx: ABCDE - BiPAP/intubate + IV immunoglobulins

27
Q

A man with a spinal cord injury at the level of T5 presents with an episode of a pounding frontal headache, flushed red skin and profuse sweating above the level of his nipple line, and a tightness in his chest.
What is the likely Dx?
How would you manage this man?
What is he at risk of developing?

A

Dx: autonomic dysreflexia

Mx: Control/remove stimulus and treat any life-threatening hypertension/bradycardia

Risk: Cerebral haemorrhage

28
Q

A 66-year-old man with a past medical history of osteoarthritis, hypertension, and lung cancer attends your clinic. He reports increasing difficulty swallowing and has felt dizzy upon standing. He says he has also been increasingly short of breath and has a longstanding productive cough. He does not report any numbness, pins and needles, or back pain. You note that he has a ‘waddling gait’ when entering the room.

Which of the following is the most likely cause of his symptoms?

How would you Ix?

How would you Mx?

A

Cx: Lambert-Eaton syndrome
Most commonly associated with lung cancer (or breast or ovarian). Antibodies attack voltage-gated Ca channels

CF:
- repeated muscle contractions lead to increased muscle strength (in contrast to myasthenia gravis)
in reality, this is seen in only 50% of patients and following prolonged muscle use muscle strength will eventually decrease
- limb-girdle weakness (affects lower limbs first)
- hyporeflexia
- autonomic symptoms: dry mouth, impotence, difficulty micturating
- ophthalmoplegia and ptosis not commonly a feature (unlike in myasthenia gravis)

Ix: EMG

Mx: Treat underlying Ca
Immunosuppressants (pred/azathioprine)
3,4-diaminopyridine is currently being trialled

29
Q

A 66 year old man presents to GP complaining of weakness in his arms that has gradually got worst over the past 2 months, he is finding it more difficult to get around the house and climb the stairs and in the past weeks his wife has told him his speech sounds slurred.

What would you expect to find on examination?
How would you diagnose him?
What Tx could you offer?

A

O/E:
LMN signs:
muscle wasting, decreased tone and reflexes, fasciculations
UMN:
increased tone, increased reflexes, up-plantar response
No sensory / eye symptoms

Dx: clinical Dx
EMG can shown decreased nerve act
Increased CK due to muscle breakdown

Tx: Riluzole - slows progression , NIV

px: 50% die within 5 years

30
Q

30 year old female presents to GP with headache and occasional blurring of vision. SHe also mentions her boyfriend has told her she sometimes goes cross eyed. She has a BMI of 35.

What is the most likely Dx?
What other RFs would you ask about?
How could you Mx?

A

Dx: idiopathic intracranial HTN

RFs:
obesity, female, pregnancy, OCP, steroid use, tetracycline, lithium

Mx: 
weight loss
Acetazolamide (diuretic)
topiramate (anti-epileptic)
optic nerve decompression surgery