Neurosurgery JC031: Paraplegia: Spinal Cord Compression, Transverse Myelitis, Spinal Dysraphism, Neuroimaging 3: Spinal Cord Flashcards

1
Q

Plegia

A

Weakness of limb

4 types:
1. Monoplegia (one limb)
2. Hemiplegia (half of body)
3. Paraplegia (lower half)
4. Tetraplegia

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2
Q

Revision: Spinal anatomy

A

31 pairs of spinal nerves:
- C1-C8 (8 pairs) (vs C1-7 vertebral bodies)
- T1-T12 (12 pairs)
- L1-L5 (5 pairs)
- S1-S5 (5 pairs)

Spinal cord ends at higher level than respective spinal canal (i.e. vertebral body)
- e.g. T10 spinal cord level = T12 / L1 vertebral body

Spinal tracts:
Ascending (Afferent / Sensory):
- **Posterior Spinothalamic tract (DC tract): Fasciculus gracilis, Fasciculus cuneatus (sacral medial, cervical lateral)
- **
Anterior, Lateral Spinothalamic tracts (Pain + Temperature) (cervical medial, sacral lateral)
- Anterior, Posterior Spinocerebellar tracts
- Spinoolivary tract
- Spinotectal tract

Descending (Efferent / Motor):
- ***Lateral Corticospinal tract (80%, main bulk of fibres) (cervical medial, lower limb lateral)
- Rubrospinal
- Reticulospinal (anterior, lateral)
- Tectospinal
- Vestibulospinal

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3
Q

Motor pathway

A

Lateral + Anterior Corticospinal tract
—> Anterior horn cells
—> Ventral nerve root (exit at each spinal level, carrying motor neurons)
(Ventral nerve root + Dorsal nerve root (Sensory modality) —> Spinal nerve root)
—> Plexus
—> Peripheral nerve innervating muscles

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4
Q

UMN vs LMN

A

UMN:
- Lesion above anterior horn cells
- Hypertonic muscle
- Clonus present
- No fasciculation
- Disuse atrophy (delayed)
- Hyperreflexic
- Up-going plantar (Babinski’s sign)

LMN:
- Lesion at ***anterior horn cells / ventral nerve root
- Hypotonic muscle
- Clonus absent
- Have fasciculation
- Acute wasting of muscles
- Hyporeflexic
- Down-going plantar

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5
Q

Myotome

A

***C3-5: Diaphragm

C5: Elbow flexors
C6: Wrist extensors
C7: Elbow extensors
C8: Finger extensors
T1: Intrinsic hand muscles

L2: Hip flexors
L3: Knee extensors
L4: Ankle dorsiflexors
L5: Long toe extensors
S1: Ankle plantar flexors

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6
Q

Sensation / Ascending tracts

A

Posterior / Dorsal column:
- Fine touch (2 point discrimination)
- Proprioception
- Pressure
- Vibration
- **Decussate in Medulla oblongata —> **Medial lemniscus —> Thalamus —> Primary somatosensory cortex in parietal lobe

Anterior, Lateral Spinothalamic tract:
- Pain
- Temperature
- **Decussate in Spinal cord —> **Anterior, Lateral Spinothalamic tract —> Thalamus —> Primary somatosensory cortex in parietal lobe

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7
Q

Sensory loss

A

Spinal nerve lesion:
- Segmental loss: ***All modalities loss at a single dermatome

Spinal cord lesion (Long tract loss):
- **Sensory level
- **
Modalities loss depends on site of lesion

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8
Q

Dermatome sensory level

A

T4: Nipple
T7: Xyphisternum
T10: **Umbilicus
L1: **
Groin / Inguinal region

C5-T1: Upper limb
L2-S2: Lower limb

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9
Q

Conus medullaris, Cauda equina

A

Conus medullaris:
- end of spinal cord proper (L1/2 vertebral level)
- Lesion at above (i.e. Spinal cord): UMN lesion
- Lesion: ***Mixed UMN + LMN lesion

Cauda equina:
- Lower lumbosacral nerve root exiting spinal cord before leaving spinal canal
- Lesion: LMN lesion

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10
Q

Cauda equina syndrome

A
  1. **Saddle anaesthesia (loss of sensation of **sacral dermatome (S2-5)
  2. **Sphincter dysfunction
    - Bladder: Painless acute urinary **
    retention
    - Bowel: ***Constipation
    - Irreversible unless very early intervention
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11
Q

Spinal cord blood supply

A
  1. Segmental artery (Segmental metameric system)
    - from **Aorta
    - paired
    - regress, prominent ones remain (Biggest: **
    Artery of Adamkiewicz: Lower thoracic, Higher lumbar level)
    - join Anterior spinal artery
  2. Anterior spinal artery
    - from **Vertebral artery in brain
    - anterior midline of spinal cord
    - anastomose with Posterior spinal artery (circumferentially + inside)
    - main contributor: **
    Artery of Adamkiewicz —> lower thoracic / upper lumbar level
  3. Posterior spinal artery
    - from ***Vertebral artery in brain
    - paired
    - posterior surface of spinal cord
    - anastomose with Anterior spinal artery (circumferentially + inside)
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12
Q

Spinal cord syndromes

A

Complete cord transaction (所有無曬)
- Complete paralysis
- Sensory loss below
- Sphincter dysfunction

Incomplete injury (Pattern of symptoms depend on location of spinal cord damaged)
1. Hemi-transection (Brown-Sequard syndrome)
2. Central cord syndrome
3. Anterior cord syndrome
4. Posterior cord syndrome
5. Variation depends on exact site of damage

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13
Q
  1. Hemi-transection (Brown-Sequard syndrome)
A

Motor:
1. Ipsilateral UMN sign (Spastic paralysis) below level of lesion (due to damage to descending lateral corticospinal tract)
(∵落黎個陣已經係medulla cross左)

  1. Ipsilateral LMN sign (Flaccid paralysis) ***at the level of lesion due to direct damage to ventral and dorsal grey matter

Sensory:
3. Ipsilateral loss of proprioceptive sensation, 2-point discrimination below level of lesion (due to damage to ascending dorsal columns)
(∵已經未去到medulla cross已經壞左)

  1. Contralateral loss of pain and temperature sensation ***a few levels below lesion (∵ at level of / a few levels below the lesion some 2nd order neurons do not cross until climb up a few levels)
    (∵爬上幾層先cross)
  2. Ipsilateral loss of ALL sensations ***at the level of lesion due to direct damage to ventral and dorsal grey matter
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14
Q

Horner’s syndrome

A

Lesion affecting ***Cervical spine, if Sympathetic trunk damaged:
1. Miosis (vs CN3 palsy: Mydriasis)
2. Ptosis
3. Enophthalmos
4. Anhydrosis (↓ sweating)

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15
Q
  1. Central cord syndrome
A

Causes:
- **Hyperextension injury
- **
Syringomyelia
- Intrinsic spinal cord tumour

Clinical features:
1. Segmental loss
- Sensory: Decussating secondary sensory neurons affected —> Bilateral Upper limb pain / numbness > Lower limb numbness

  1. Long tract sign
    - Medial fibres affected first (cervical fibres)
    - Motor: Upper limb > Lower limb weakness
    - ***Sacral sparing

(MUDS:
- **Motor > Sensory
- **
Upper > Lower limb
- ***Distal > Proximal
- Extension injury)

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16
Q
  1. Anterior cord syndrome
A

Causes:
- Anterior spinal artery infarct
- External compression

Clinical features:
1. **Paraplegia (damaged motor tract + anterior horn cells)
2. **
Spinothalamic loss
3. ***Intact proprioception, 2 point discrimination (fine touch) (∵ Intact Dorsal column)

17
Q
  1. Posterior cord syndrome
A

Rare

Clinical features:
1. Pain and paresthesia in upper limb + trunk (∵ **spared pain + temperature sensation)
2. **
Bilateral loss of fine touch, proprioceptive, vibration sensation below the lesion
3. Motor: Mild UL paraparesis

18
Q

Grading severity of injury: American Spinal Injury Association (ASIA) Classification

A

A to E:
- A: Complete spinal cord injury (no sensory / motor function preserved below level)
- E: Normal (sensory / motor function preserved)

Sensory: Pinprick (Spinothalamic) + Touch (DC) in each dermatome

19
Q

Spinal shock

A

2 meanings:
1. **Flaccid paralysis + **Areflexia for 1-2 weeks after injury
- Acute damage to spinal cord —> ***Denervation response —> Completely Areflexic + Weak muscle tone
- Return of anal tone / reflex usually signifies end of spinal shock —> Can properly assess motor + sensory function again —> Determine permanent deficits
- Phase 1 (0-1 day): Areflexia (Loss of descending facilitation)
- Phase 2 (1-3 day): Initial reflex return (Denervation supersensitivity)
- Phase 3 (1-4 week): Initial Hyperreflexia (Axon-supported synapse growth)
- Phase 4 (1-12 month): Final Hyperreflexia (Soma-supported synapse growth)

SpC Revision:
- Period of temporary loss of function after injury (hours - days)
- No motor / sensory function: cannot differentiate between complete / incomplete injury
- All reflexes absent
- Spinal shock is over if bulbocavernosus / anal wink reflex has returned (these are lowest local reflexes mediated by spinal cord level)
- Assess for motor / sensory function ONLY after spinal shock is over

(Web:
- loss of muscle tone and spinal reflexes below the level of a severe spinal cord lesion
- this “shock” does not imply a state of circulatory collapse (vs neurogenic shock) but of suppressed spinal reflexes below the level of cord injury
- it takes between days and months for spinal shock to completely resolve —> when it does, the flaccidity that was once seen gradually becomes ***spasticity (UMN lesions))

  1. Neurogenic shock
    - **Sympathetic signal disruption in C1-T1
    —> Sudden of sympathetic tone
    —> **
    Vasodilation, Hypotension, Bradycardia, Warm, Flushed skin
    —> Shock, Hypoperfusion of body
    —> Require resuscitation
    - C5 or below: affect Diaphragmatic breathing (Diaphragm innervated by C3-5)
    - Above C3: ***Respiratory arrest (cannot breathe at all)
    —> Require intubation, mechanical ventilation, cardiopulmonary support
20
Q

Causes of Spinal cord injury

A

By Pathology (VINDICAT):
1. Vascular
2. Infective
3. Neoplastic
4. Degenerative
5. Inflammation
6. Congenital
7. Autoimmune
8. Trauma

21
Q
  1. Vascular causes
A
  1. ***Spinal cord infarct (arteries supplying spinal cord occluded)
    - Aortic surgery: EVAR, AAA repair
    - Spontaneous
  2. ***Spinal AVM
    - mass effect compression
    - haemorrhage into spinal cord
22
Q
  1. Infective causes
A
  1. Spinal ***abscess
  2. Meningitis affecting spinal cord
  3. TB spine
  4. ***Osteomyelitis (e.g. IVDU, DM, HIV)
23
Q
  1. Neoplastic causes
A

Extradural tumour
1. Spinal metastasis
- >90% Vertebral
- Commonly from Breast, Lung, Prostate
- Commonly ***Thoracic spine
- Compress spinal canal + spinal cord within it

Route:
- **Haematogenous spread
- **
Direct invasion e.g. Paraspinal lung Ca
- **Lymphatic: along root sleeves
- Subarachnoid seeding via **
CSF from primary and secondary CNS neoplasms

Intradural extramedullary tumour
2. Meningioma
- Middle age
- F>M
- Thoracic
- Associated with ***NF-2

  1. Schwannoma
    - Cervical + Lumbar
    - NF-2 (multiple schwannoma along spine)
    - ***Radicular pain + **Sensory loss
    - Weakness less common
    - Cord compression if large

Intramedullary tumour
4. Spinal ependymoma
- Commonest **Primary cord tumour in adults
- Male
- NF-2
- WHO grade 2/3 (mostly)
- **
Slow growing, discreet, well-circumscribed (can be resected)
- ***Compression (vs infiltrating) the cord

  1. Spinal astrocytoma
    - 2nd most common **Primary cord tumour
    - Children (60% lesions)
    - Lower grade lesions than in brain
    - Faster growing than ependymoma
    - **
    Infiltrative —> Complete excision less likely
24
Q

Treatment for Spinal tumours

A
  1. Surgical resection within safety limit
    - Intraoperative monitoring
    - Motor evoked potential (MEP) and Somatosensory evoked potential (SSEP)
    —> guide extent of surgery + preserve normal neurological function
  2. Adjuvant therapy for some
    - External beam radiation therapy (***ERT)
  3. Metastasis
    - Primarily ERT
    - Surgery for pain, instability, lesions resistant to RT —> Palliative in nature
25
Q
  1. Degenerative causes
A

Spondylosis
- **Disc degeneration / prolapse —> Compression
- Apophyseal (Facet) joint damage / hypertrophy —> Instability, **
Spondylolisthesis —> Narrow spinal canal —> Compression

***Ossified / Hypertrophied Spinal ligaments —> Compression

26
Q

Spondylitis vs Spondylosis vs Spondylolisthesis vs Spondylolysis

A

Spondylitis:
Vertebral inflammation

Spondylosis:
Vertebral degeneration

Spondylolisthesis:
Vertebral slippage

Spondylolysis:
Anatomic defect or break of the pars interarticularis of the vertebral arch

27
Q
  1. Inflammation causes
A
  • **Transverse myelitis
  • caused by ***Multiple sclerosis / other causes
  • **↑ CSF protein, **CSF pleocytosis, MRI hyperintense area
28
Q

Spondylosis and Myelopathy

A
  • Signs of cervical myelopathy
  • Cord compression
  • Complete / Incomplete cord damage
  • Chronic progressive / Acute exacerbation (e.g. trauma)

Treatment:
1. Conservative management (mild symptoms / no neurological deficits)
- Analgesia
- Physiotherapy

  1. Surgical decompression
    - **Progressive neurological deficit
    - **
    Myelopathy / Radiculopathy
    - Intractable pain
29
Q
  1. Congenital causes
A

Spinal dysraphism (neural tube defect: cannot close completely)
1. **Myelomeningocele (Spinal cord + Nerve root + Meninges protrude out of spinal canal)
2. **
Meningocele (Only Meninges protrude)
3. **Spina bifida occulta
—> Conus + Filum terminale can be affected by malformation (e.g. Lipoma formation)
—> Traction in spinal cord
—> **
Tethering syndrome

30
Q

Tethered cord syndrome

A
  • Common in Spina bifida occulta
  • Anchoring of lower end of spinal cord by:
    —> **Lipoma
    —> **
    Fatty filum terminale
  • ***Low-lying Conus medullaris (at L3/4, normally rise up to L1 level)
  • Cord under tension as spine lengthens
    —> Progressive neurological deficit
    —> **Lower limb LMN weakness + **Sphincter dysfunction + Pain + Scoliosis + Foot deformity

Clinical presentation:
- Deterioration at growth spurt (***<2/3 yo or puberty)

Investigation:
- Early detection with MRI
- Urodynamic study

Treatment:
- Surgical untethering before clinical deterioration

31
Q
  1. Trauma causes
A
  1. Road traffic accident
  2. Fall
  3. Assault
  4. Sports / Recreation related injury
  5. Others
  • 50% ***Cervical spine (∵ most mobile + weakest)
  • 25% associated with other organ injuries (e.g. head)
  • 15% associated with non-adjacent level injuries
32
Q

Spinal trauma classification

A

According to different pattern of force
1. Vertical compression (e.g. load fall onto head)
- watch out for cord impingement e.g. ∵ **retropulsion of vertebral body fragment compressing **anterior cord

  1. Hinge injury (e.g. blow to head)
    - Ligament intact / disrupted
  2. Shearing injury (e.g. fall from height)

According to stable / unstable
Stable:
- Vertical compression
- Hinge injury with intact ligament

Unstable:
- Shearing injury
- Hinge injury with disrupted ligament (need early fixation of spine)

33
Q

Other injury causes

A

Epidural haematoma
- compressing on spinal cord

34
Q

Prognosis of Spinal cord injury

A

Complete injury:
- Poor
- Recovery rare

Incomplete injury:
- Difficult to predict
- Most recovery occur within ***6 months
- Depending on level and extent of injury
- Many can eventually walk (with aids)

35
Q

Other complications associated with Spinal cord injury

A
  1. ***Limb spasticity
    - can be painful
  2. Pressure sore
  3. ***Neurogenic bladder
    - Repeated episodes of UTI
    - Reflux nephropathy
  4. ***Anal function
    - Constipation
  5. ***Sexual function
  6. **Autonomic dysreflexia
    - Autonomic dysfunction e.g. **
    sudden sympathetic storm —> high BP, Temperature, Tachycardia, Sweating
  7. ***Temperature control
    - Impaired homeostasis
36
Q

Summary

A
  • Acute paraplegia is an Emergency!
  • Where is the lesion —> Anatomy (Dermatome, Myotome, Ascending / Descending tracts, Central / Anterior / Posterior cord)
  • What is the lesion —> VINDICATE
  • Spinal cord is unforgiving
    —> Significant disability
    —> Complete injury / with Sphincter function loss —> Very poor prognosis