Spinal Cord Lesions Flashcards

1
Q

What are motor descending pyramidal tract
- Pass through pyramid of medulla

What is pattern of weakness

A

Anterior and Lateral corticospinal = 90%
Also corticobulbar

Extensor weaker in arms and flexor in legs

UMN originate at either motor cortex or brain stem nuclei
Travel to anterior horn cell in spinal cord at target level

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2
Q

What are extra pyramidal motor tracks

- Don’t pass through pyramid

A

Rubrospinal
Reticulospinal
Vestibulospinal

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3
Q

What are sensory descending tracts in dorsal column

A

Gracile fasiculus

Cuneate fasicullus

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4
Q

Sensory spinocerebelllar

A

Anterior

Posterior

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5
Q

Sensory spinothalamic

A

Anterolteral tract
Lateral
Anterior

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6
Q

What causes pure motor signs

A

MND

Poliomyelitis

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7
Q

How does motor neurone present

A

Corticospinal tracts

UMN and LMN signs

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8
Q

What does poliomyelitis affect

A

Anterior horn cell

LMN signs

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9
Q

How can sensory present

A

Dorsal column

Spinothalamic

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10
Q

If spinothalamic affected what are the signs

A

Loss of pain, temp and sensation

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11
Q

If dorsal column affected what are the signs

A

Loss of proprioception and vibration

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12
Q

What affects dorsal

A

Tabes dorsalis - late consequence of syphillis
SACD
Spinal cord infarction

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13
Q

What happens if spinothalamic lesion

A

Loss of pain, temp and sensation

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14
Q

What causes combined UMN and LMN signs

Fred
Tabby
Cat 
Seeks 
Mice
A
Fredreich ataxia
Tabes dorsalis (syphillis) 
Cervical + lumbar spondylosis
SACD- B12
Motor neurone disease 

Alnord chiari malformato / syndomyelia

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15
Q

What is Brown Squared

A

Spinal cord hemisection

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16
Q

What tracts are affected

A

Lateral corticospinal
Dorsal
Lateral Spinothalamic

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17
Q

What does it lead too

A

Ipsilateral spastic paralysis below lesion (corticospinal) + UMN signs
Ipsilateral loss of proprioception and vibration (dorsal)
Ipsilateral sensory loss
Contralateral loss of pain and temp (spinothalamic)

18
Q

What does cord compression lead too

19
Q

What can cause

A

Malignancy
Haematoma
Fracture

20
Q

What causes subacute combined degeneration of spinal cord (SCAD)

A

B12 / thiamine deficiency

  • Pernicious - Ab against intrinsic factor
  • Chron’s
  • Gastrectomy
21
Q

What tracts are affected

A

Lateral corticospinal
Dorsal
Spinocerebellar

22
Q

What does it cause

A

Bilateral spastic paralysis
Bilateral loss of proprioception and vibration - usually first
Distal paraesthesia after
Bilateral limb ataxia
UMN and LMN signs in leg - extensor plantar / absent knee / absent ankle reflex (hyporeflexia)
Painess urine retention
Pain and temp often remain intact

23
Q

What does Fredreich’s ataxia cause

A

Same as above

Also cerebellar ataxia signs

24
Q

What is syringomyelia

A

Collection of cerebrospinal fluid in spinal cord

Symptoms may be static for years but worsen fast e.g. on coughing or sneezing

25
What can cause
Tumour Trauma Arnold Chiari malformation
26
What tracts are affected
Antero-Lateral spinothalamic as fluid in middle of cor where this tract passes
27
What does it cause
``` Progressive slow neuro signs Flaccid paralysis (typically hand) Loss of pain and temp but preserved touch / vibration Wasting and weakness of hands Cape like distribution Paraesthesia Hyporeflexia Neuropathic pain Upgoing plantar Bladder. / bowel Horner due to compression of sympathetic but rare ```
28
What is classic presentation
Burning hand without realising
29
What happens if not Rx
Scoliosis
30
How do you Dx
Spine MRI for tumour | Brain MRI for CHairi
31
How do you Rx
Treat cause | Shunt
32
How does MS present
Asymmetrical combination of motor, sensory and ataxia signs
33
What tracts affecting in anterior spinal artery occlusion
Lateral corticospinal | Lateral spinothalamic
34
What does it cause
Bilateral spastic paresis | Bilateral loss of pain and temp
35
What is Alnord Chiari malformation
Downward displacement of cerebral tonsil through foramen magnum Congenital Trauam
36
What does it cause
Synrigmyelia Non-communicating hydrocephalus Headache
37
What is Fredreich's ataxia
AR trinucleotide disorder that causes spinocerebellar degeneration Anticipation
38
How does it present
Present teens UMN and LMN signs e.g. absent ankle jerk + extensor plantar + Ataxia ``` Other Kyphoscolisosis Optic atrophy HOCM DM Associated with WPW ```
39
What is Telangiectasia ataxia
AR defect in gene for DNA repair + immunodeficiency
40
What does it cause
``` Early childhood Abnormal movement Ataxia Telangiectasia IgA deficient so recurrent infection ```
41
What is Leg term risk
Leukaemia