Four limb weakness Flashcards

(34 cards)

1
Q

What produces UMN signs and what are they?

A

Lesions to the brain, brainstem and spinal cord

Bulk - normal
Tone - Increased
Power - reduced
Abnormal movement - fasciculations not seen
Reflexes - Brisk
Plantar/Babinski - Up-going
Clonus - +ve
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2
Q

What produces LMN signs and what are they?

A

Lesions to the LMN, anterior horn cell nerve root or peripheral nerve

Bulk - atrophy
Tone - decreased
Power - reduced
Abnormal movement - fasciculations
Reflexes - decreased/absent
Plantar/Babinski - down-going
Clonus - -ve
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3
Q

When can mixed UMN and LMN signs occur?

A

MND
B12 deficiency
taboparesis

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4
Q

What is spinal shock?

A

When someone has an acute insult to the cord (vascular, trauma, haemorrhage) it can cause LMN features

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5
Q

What tracts are affected in anterior cord syndrome?

A
  • Lateral corticospinal tracts

* Lateral spinothalamic tracts

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6
Q

What are the features of anterior cord syndrome?

A
Bilateral loss below level of lesion:
o	Motor function
o	Light touch
o	Pain
o	Temperature
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7
Q

What are the features of central cord syndrome?

A
MUD-E
•	Motor > sensory
•	Upper extremity > lower extremity
•	Distal > proximal
•	Extension injury
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8
Q

What tracts are affected in hemi-cord/Brown-Sequard syndrome?

A
  • Lateral corticospinal
  • Dorsal columns
  • Lateral spinothalamic
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9
Q

What are the features of hemi-cord/Brown-Sequard syndrome?

A

Ipsilateral loss below lesion
o Motor function – spastic paraparesis
o Proprioception – sensory ataxia
o Vibration

Contralateral loss below lesion – spinothalamic tract decussates
o Pain
o Temperature

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10
Q

What is subacute combined degeneration of the spinal cord?

A

Vitamin B12 or E deficiency causing degeneration of the posterior and lateral columns of the cord

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11
Q

What tracts are affected in subacute combined degeneration of the spinal cord?

A
  • Lateral corticospinal
  • Doral columns
  • Spinocerebellar
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12
Q

What are the features of subacute combined degeneration of the spinal cord?

A
Bilateral:
o	Motor – UMN signs 
o	Proprioception and vibration
o	Limb ataxia 
o	Absent ankle and knee jerks
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13
Q

What is Friedrich’s ataxia and what symptoms does it produce?

A

Inherited condition

Same symptoms as subacute combined degeneration of the spinal cord with an intention tremor

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14
Q

What is syringomyelia and what is it associated with?

A

Fluid-filled cyst forms within the spinal cord causing compression due to dilation of CSF space within spinal cord

Chiarai 1 malformation

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15
Q

What does syringomyelia affect in the spinal cord?

A
  • Ventral horns

* Lateral spinothalamic

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16
Q

What are the features of syringomyelia?

A
  • LMN signs

* Cape-like Bilateral Loss of pain and temperature

17
Q

What does neurosyphilis cause?

A

Degeneration of dorsal columns:

• Loss of proprioception and vibration

18
Q

What does compression of C5 and above cause?

A
  • UMN signs
  • Sensory loss in all 4 limbs
  • Diaphragmic weakness
  • Autonomic dysfunction - incontinence
19
Q

What does compression of C5-T1 cause?

A
  • LMN signs in upper limbs
  • Sensory loss below level of lesion
  • UMN signs in legs
  • Respiratory (intercostal) weakness
  • Autonomic dysfunction – urinary incontinence
20
Q

What does compression of thoracic vertebrae cause?

A
  • Spastic paraplegia
  • Sensory level on trunk
  • Weakness of legs
  • Sacral loss of sensation
  • Extensor plantar responses
21
Q

What does compression of Cauda equina/below T12/L1 above cause?

A
  • LMN signs
  • New onset bilateral sciatica
  • New/worsening Back pain
  • Saddle area anaesthesia
  • Decreased anal sphincter tone
  • Urinary retention
22
Q

What can cause acute transverse myelitis?

A

inflammation of the spinal cord

Inflammatory
o MS, post-infective, NMO/Devic’s
o CTD related (lupus, sjogren’s, sarcoid)

Compressive
o Discs, tumours

Infective
o	Viral (HZV, HIV)

Metabolic
o B12, copper deficiency

23
Q

What is GBS?

A

B-cells produce antibodies against a pathogen that target myelin sheath, motor nerve cell or axon

24
Q

What is the presentation of GBS?

A
  • Peripheral loss of sensation or neuropathic pain
  • Symmetrical ascending weakness (starting at the feet and moving upwards)
  • Reduced reflexes
25
What are the other features of GBS?
* Hx gastroenteritis * Respiratory muscle weakness * CN involvement * Autonomic involvement
26
What do nerve conduction studies and lumbar puncture show for GBS?
Nerve conduction studies: o Slow motor nerve conduction velocity (demyelination) o Prolonged/absent F waves o Prolonged distal motor latency Lumbar puncture o Increased protein o Normal WBC count and glucose
27
How do you manage GBS?
* IV immunoglobulins * Plasma exchange * Supportive care * VTE prophylaxis
28
What is miller fisher syndrome and how does it present?
Variant of Guillain-Barre syndrome Descending paralysis: • Ophthalmoplegia • Areflexia • Ataxia
29
What is Charcot-marie-tooth disease
AD peripheral neuropathy | - LMN and sensory signs
30
What is MND?
Progressive degeneration of UMN and LMN | No sensory loss of sphincter distrubance
31
What is Amyotrophic lateral sclerosis (ALS)?
Loss of motor neurones in motor cortex and anterior horn of the cord o LMN signs in arms UMN signs in legs
32
What is Progressive bulbar palsy?
Palsy of tongue, muscles of mastication and facial muscles | o Loss of brainstem motor nuclei (IX-XII)
33
What is Progressive muscular atrophy?
Anterior horn cell lesion | o LMN signs only
34
What is Primary lateral sclerosis?
Loss of Betz cells in motor cortex | o UMN signs only