Neuro revision Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What is syringomyelia?

A

Collection of cerebrospinal fluid within spinal cord

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

Causes of syringomyelia?

A

Chiari malformation
Trauma
Tumours
Idiopathic

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

In syringomyelia which sensation is affected?

A

Cape- like loss of temperature sensation, preservation of light touch, proprioception and vibration

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

Clinical features of syringomyelia?

A

Cape- like loss of temperature sensation
Spastic weakness
Neuropathic pain
Upgoing plantars
autonomic features
Horner’s syndrome
Scoliosis

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

Treatment for generalised tonic clonic seizures?

A

Males - sodium valproate
Females - lamotrigine or levetiracetam

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Treatment for absence seizures?

A

1st line = ethosuximide
2nd = male - sodium valproate
female - lamotrigine/ levetiracetam

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

Treatment for focal seizures?

A

First line = lamotrigine or levetiracetam
Second line = carbamexapine, oxycarbazepine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Which medication may exacerbate absence seizures?

A

Carbamezapine

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

What is another name for absence seizures?

A

Petit mal

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

Treatment for myoclonic seizures?

A

Males - sodium valproate
Females - levetiracetam

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Treatment for tonic or atonic seizures?

A

Males - sodium valproate
Females - lamotrigine

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

What nerves does the sciatic nerve divide into?

A

Tibial and common peroneal nerves

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

Where does injury often occur in common peroneal nerve lesion?

A

Neck of fibula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Characteristics of common peroneal nerve lesion?

A

Foot drop
Weak foot dorsiflexion, foot eversion
Weak extensor hallucis longus
Sensory loss over dorsum of foot, and lower lateral leg
Wasting of anterior tibial and peroneal muscles

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

Factors suggesting true epileptic seizure?

A

Tongue biting
Raises serum prolactin

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

Factors suggesting pseudoseizure?

A

Pelvic thrusting
Family member with epilepsy
Female&raquo_space;
Crying after seizure
Don’t occur when alone
Gradual onset

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

Classic history - vestibular schwannoma/ acoustic neuroma?

A

Vertigo
Unilateral SNHL
Tinnitus
Absent corneal reflex

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

Interpretation of Webers?

A

Normal - midline
Conductive - bad ear
SNHL - good ear

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

Which artery occluded in lateral medullary syndrome/ Wallenberg’s?

A

Posterior inferior cerebellar artery

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

Cerebellar features of posterior inferior cerebellar artery occlusion/ lateral medullary syndrome?

A

Cerebellar: ataxia, nystagmus

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

Brainstem features of posterior inferior cerebellar artery occlusion/ lateral medullary syndrome?

A

Ipsilateral: Dysphagia, facial numbness, cranial nerve palsy e.g. Horner’s
Contralateral: limb sensory loss

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

What is Guillain- Barre syndrome?

A

Immune mediated demyelination of peripheral nervous system, often triggered by infection

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

Which infection often causes GBS?

A

Campylobacter jejuni

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

What is the characteristic feature of GBS?

A

Progressive, symmetrical weakness of all limbs
Classically ascending weakness
Reduced/ absent reflexes
Few sensory signs/ symptoms

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

Investigations in GBS?

A

Lumbar puncture - rise in protein, normal WBC count
Nerve conduction studies - dec motor nerve conduction velocity (demyelination)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Parietal lobe lesions?

A

Sensory inattention
Apraxia
Tactile agnosia
Inferior homonymous quadrantanopia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Occipital lobe lesion?

A

Homonymous hemianopia (with macular sparing)
Cortical blindness
Visual agnosia

27
Q

Temporal lobe lesion?

A

Wernicke’s aphasia
Superior homonymous quadrantanopia
Auditory agnosia
Prosopagnosia (difficulty recognising faces)

28
Q

Frontal lobe lesion?

A

Broca’s aphasia (expressive)
Disinhibition
Perseveration
Anosmia
Inability to generate list

29
Q

Cerebellum lesions?

A

Midline - gait and truncal ataxia
Hemisphere lesion - intention tremor, past pointing, dysdiadokinesia, nystagmus

30
Q

Dysdiadochokinesia?

A

Inability to perform rapid alternating muscle movements

31
Q

Cause of brown sequard syndrome?

A

Lateral hemisection of the spinal cord

32
Q

Features of brown squared syndrome?

A

Ipsilateral weakness below lesion
Ipsilateral loss of proprioception and vibration sensation
Contralateral loss of pain and temperature sensation

33
Q

Does unilateral cerebellar lesion cause contra or ipsi- lateral signs?

A

Ipsilateral

34
Q

Symptoms of cerebellar disease?

A

DANISH
D- dysdiadochokinesia,, dysmetria (past- pointing), ‘drunk’
A- ataxia
N- nystagmus
I- intention tremor
S- slurred staccato speech, scanning dysarthria
H - hypotonia

35
Q

GCS - motor response?

A
  1. Obeys commands
  2. Localises to pain
  3. Withdraws from pain/ normal flexion
  4. Abnormal flexion to pain (decorticate posture)
  5. Extending to pain
  6. None
36
Q

GCS - verbal?

A
  1. Orientated
  2. Confused
  3. Words
  4. Sounds
  5. None
37
Q

GCS - eye opening?

A
  1. Spontaneous
  2. To speech
  3. To pain
  4. None
38
Q

What can Lambert- Eaton syndrome be associated with?

A

Small cell lung cancer&raquo_space;>
Breast, ovarian cancer
Independent autoimmune disorder

39
Q

Cause of Lambert- Eaton syndrome?

A

Antibody against presynaptic voltage- gated calcium channels in PNS

40
Q

Features of Lambert- Eaton syndrome?

A

Repeated muscle contractions lead to inc muscle strength
Limb- girdle weakness
Hyporeflexia
Autonomic symptoms

41
Q

EMG in Lambert- Eaton syndrome?

A

Incremental response to repetitive electrical stimulation

42
Q

Management of Lambert- Eaton syndrome?

A

Treat underlying
Immunosuppression e.g. prednisolone +/- azathioprine

43
Q

What is myasthenia gravis?

A

Autoimmune disorder resulting in insufficient functioning acetylcholine receptors

44
Q

What causes myasthenia gravis?

A

Antibodies to acetylcholine receptors seen in 85-90%

45
Q

Key features of myasthenia gravis?

A

Muscle fatigability
Extraocular muscle weakness: diplopia
Proximal muscle weakness
Ptosis
Dysphagia

46
Q

Associations with myasthenia gravis?

A

Thymomas
AI disorders e.g. pernicious anaemia, AI thyroid disorders, rheumatoid, SLE
Thymic hyperplasia

47
Q

Investigations for myasthenia gravis?

A

Single fibre EMG
CK normal
Antibodies to acetylcholine receptors, some + for anti- muscle- specific tyrosine kinase AB’s

48
Q

Management of myasthenia gravis?

A

Long- acting acetylcholinesterase inhibitors - pyridostigmine
Eventually require immunosuppression - prednisolone, azathioprine
Thmectomy

49
Q

Management of myasthenia crisis?

A

Plasmapharesis
IV immunoglobulins

50
Q

Ankle reflex?

A

S1-S2

51
Q

Knee reflex?

A

L3-L4

52
Q

Biceps reflex?

A

C5-C6

53
Q

Triceps reflex?

A

C7-C8

54
Q

What causes subacute combined degeneration of the spinal cord?

A

Vitamin B12 deficiency resulting in impairment of dorsal columns, lateral corticospinal tracts and spinocerebellar tracts

55
Q

Features of subacute combined degeneration of the spinal cord - dorsal column?

A

Distal tingling/burning/sensory loss is symmetrical and tends to affect the legs more than the arms
Impaired proprioception and vibration sens

56
Q

Features of subacute combined degeneration of the spinal cord - lateral corticospinal tract?

A

Muscle weakness, hyperreflexia, and spasticity
upper motor neuron signs typically develop in the legs first
Brisk knee reflexes
absent ankle jerks
extensor plantars

57
Q

Features of subacute combined degeneration of the spinal cord - spinocerebellar tracts?

A

Sensory ataxia - gait abnormalities
Positive Romberg’s sign

58
Q

Anterior cerebral artery stroke?

A

Contralateral hemiparesis and sensory loss, lower extremity > upper

59
Q

Middle cerebral artery stroke?

A

Contralateral hemiparesis and sensory loss, upper extremity > lower
Contralateral homonymous hemianopia
Aphasia

60
Q

Posterior cerebral artery stroke?

A

Contralateral homonymous hemianopia with macular sparing
Visual agnosia

61
Q

Weber’s syndrome/ branches of posterior cerebral artery that supply midbrain?

A

Ipsilateral CN III palsy
Contralateral weakness of upper and lower extremity

62
Q

Posterior inferior cerebellar artery (lateral medullary syndrome, Wallenberg’s syndrome)

A

Ipsilateral: facial pain and temperature loss
Contralateral: limb/torso pain and temperature loss
Ataxia, nystagmus

63
Q

Anterior inferior cerebellar artery (lateral pontine syndrome)?

A

Similar to Wallenberg’s
Ipsilateral: facial paralysis and deafness

64
Q

Lacunar stroke?

A

Isolated hemiparesis, hemisensory loss or hemiparesis with limb ataxia
Strong assoc. w/ hypertension
Basal ganglia, thalamus, internal capsule