Spinal Cord Compression Flashcards

1
Q

what is the clinical features of complete spinal cord transection?

A

All sensory modalities and reflexes impaired below level of severance: pinprick loss most valuable Flaccid, paraplegia or tetraplegia
Fasciculations
Urinary or rectal sphincter dysfunction
Sweating, piloerection diminished below lesions
Genital reflexes lost, priapism

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2
Q

what are the clinical features of central cord syndrome?

A

Vest-like loss of pain and temperature
Initial sparing of proprioception
Sacral sensation spared
Paraparesis or tetraparesis

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3
Q

what are the clinical features of cord hemisection?

A
  • Ipsilateral upper motor neuron paralysis and loss of proprioception (dorsal column) below the lesion.
  • Contralateral loss of pain and temperature sensation beginning at 1 or 2 segments below the lesion.
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4
Q

what are the clinical features of anterior cord syndrome?

A

· Pain and temperature loss below lesion
· Proprioception spared
· Flaccid, areflexia
· Paraparesis or tetraparesis
· Fasciculations
· Urinary or rectal sphincter dysfunction
· Dysautonomia absent

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5
Q

what are the features of UMN symptoms in cord hemisection?

A

o signs maximal on side of lesion.
o Weakness in a ‘pyramidal’ distribution
 arms – extensors predominantly affected
 legs – flexors predominantly affected.
o Increased tone, clonus – increased reflexes
o Extensor plantar response

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6
Q

what are the causes of central cord syndrome?

A

Acute extension or flexion injury to already stenotic neck or syringomyelia or tumour

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7
Q

why is upper limb weakness more common than lower limb in central cord syndrome?

A

the fibres supplying the upper limbs in the lateral corticospinal tracts are more medial to the fibres supplying the lower limbs, hence a lesion in the central cord is more likely to damage the upper limb fibres

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8
Q

what tracts are affected as the lesion expands in central cord syndrome?

A

anterior horn cells are also involved and a l.m.n weakness occurs

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9
Q

what happens when corticospinal tracts are involved in central cord syndrome?

A

u.m.n signs and symptoms in the limbs below the level of lesion

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10
Q

what are the acute causes of spinal cord compression?

A

Trauma, tumours, infection, spontaneous haemorrhage

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11
Q

what are the types of spinal cord trauma?

A

Vertical Compression = burst fracture (stable)
Hinge Injury – weight falling on back or blow to the head (stable or unstable)
Shearing Injury – fall from height or RTA (unstable)
Hyperextension injury – rupture of anterior longitudinal ligament (stable in flexion)

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12
Q

what are the clinical features of spinal cord compression caused by trauma?

A

tenderness over spinous process, paraspinal swelling or a gap between the spinous process
neurogenic paradoxical ventilation
bilateral absence of limb reflexes in flaccid limbs, unresponsive to painful stimuli indicates spinal cord damage
painless urinary retention or priapism

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13
Q

how is spinal cord trauma diagnosed?

A

 X Rays – lateral view and AP (if in doubt take oblique)
 CT Scanning
 MRI

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14
Q

how is spinal cord trauma managed?

A

unstable lesions require either operative fixation or immobilisation
METHYLPREDNISOLONE – bolus, 24hr infusion

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15
Q

how is spinal cord trauma of odontoids managed?

A

immobilisation to avoid non-union = Halo (posterior C1, C2 fusion if non-union)

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16
Q

how is spinal cord trauma of cervical spine managed?

A
  • if cord damage – traction (tongs/callipers inserted into skull)
  • if cord intact + stable = cervical collar
  • If cord intact + unstable = operative fixation or 12 weeks skull traction or halo
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17
Q

how is spinal cord trauma of thoracic spine managed?

A
  • stable – normal activity after pain subsides

* unstable – no treatment other than for paraplegia

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18
Q

how is spinal cord trauma of thoracolumbar region managed?

A
  • stable = mobilise
  • unstable – operative reduction and fixation (anterior and/or posterior e.g. Hartshill rectangle or screw/rod construct)
  • Unstable – conservative – without paraplegia = brace, with paraplegia = bed rest
19
Q

how do tumours cause spinal cord compression?

A

collapse or haemorrhage

20
Q

what are the causes of spinal cord compression via infection?

A

o surgery or trauma

o epidural abscess

21
Q

what are the common organisms involved in spinal cord infection?

A
  • staph aureus most common

* ALSO, TB

22
Q

how does TB spread in the spine?

A

lower thoracic spine effected and initially affects the intravertebral discs and spreads to vertebral bodies

23
Q

how does infection generally spread in spine?

A

Haematogenous spread or from vertebral osteomyelitis

24
Q

what are the clinical features of epidural abscess of spine?

A
  • mimics extradural tumour or haematoma with bilateral leg weakness, sensory level and urinary retention
  • very severe pain and tenderness
  • toxaemia; pyrexia, malaise, increased pulse rate
  • rigidity of neck and spinal column with marked resistance to flexion
  • if TB – classic symptoms often absent
25
Q

how are epidural abscess of spine diagnosed?

A
  • X-ray, MRI

* CSF, leucocytosis, blood cultures

26
Q

what is the management of epidural spinal abscess?

A

• antimicrobial therapy, surgical drainage, stabilisation where required

27
Q

what are causes of spontaneous haemorrhage?

A

Epidural, Subdural, Intramedullary, Trauma, Bleeding diatheses, Anticoagulants, AVM

28
Q

what are the causes of spinal cord infarction?

A
  • small vessel disease – diabetes, vasculitis, neurosyphilis, endarteritis
  • large vessel disease – atheromatous, embolic, thrombotic, Dissection, hypotension
29
Q

what are the clinical features of anterior spinal cord infarction?

A

DEPENDENT ON level, radicular pain at onset, sudden para/quadplegia, flaccid limbs → spastic, areflexia → hyper-reflexia and extensor plantar responses, preserved vibration and proprioception, urinary retention

30
Q

what are the clinical features of posterior spinal cord infarction?

A

loss of tendon reflexes/motor weakness, loss of proprioception

31
Q

what is the management of spinal cord infarction?

A

reverse anticoagulation, surgical decompression

32
Q

what are the causes of chronic spinal cord compression?

A

degenerative disease (spondylosis)
tumours
RA

33
Q

what are the causes of spinal cord stenosis?

A

osteophyte formation
bulging of intervertebral discs
facet joint hypertrophy
subluxation

34
Q

what are the clinical features of cervical spinal prolapse?

A

LMN, arm pain, dermatomes, myotomes

35
Q

what are the clinical features of thoracic spinal prolapse?

A

o rare
o thoracic pain
o usually central causing myeolopathy

36
Q

what are the clinical features of lumbar disc prolapse?

A

mechanical (spinal movements restricted, scoliosis present, lumbar lordosis lost), unable to straight leg raise, neurological deficit, numbness of parenthesis in distribution

37
Q

what is the pathophysiology of lumbar disc prolapse?

A

tear in annulus fibrosis leads to soft nucleus herniating causing irritation + compression to SC. Most common to herniate posterolateral. LMN

38
Q

what is the management of degenerative spinal stenosis?

A

surgical decompression +/- stabilisation

39
Q

what are the types of extradural spinal cord tumours?

A

usually metastasis of lung, breast, kidney, prostate

40
Q

what are the types of intradural spinal cord tumours?

A
  • extramedullary – meningioma, schwannoma

* intramedullary – astrocytoma, ependymoma

41
Q

what are the clinical features of spinal tumours?

A

bone pain and tenderness, preceding limb and autonomic dysfunction

42
Q

what investigations are used to diagnose spinal tumours?

A

X-ray, MRI, PET Scan

43
Q

what is the management of metastatic spinal tumours?

A

depends on patient and tumour, dexamethasone, radiotherapy, chemotherapy, surgical decompression and stabilisation

44
Q

what is the management of primary spinal tumours?

A

surgical excision