Spinal Cord Lesions Flashcards
1
Q
Complete spinal cord syndrome - cervical cord
A
- Can result from trauma, degenerative disease, inflammation, infection or tumour
- All descending motor and ascending sensory tracts disrupted
- Motor - spastic tetraparesis
- Reflexes - brisk below level of lesion
- Sensory - loss of all modalities below lesion
- Plantars - extensor response bilaterally
- Breathing - affected in high cervical lesions
- Remember spinal shock and sphincter disturbance
2
Q
Complete spinal cord syndrome - thoracic cord
A
- Can result from trauma, degenerative disease, inflammation, infection or tumour
- All descending motor and ascending sensory tracts disrupted
- Motor - spastic paraparesis
- Reflexes - brisk in lower limbs
- Sensory - loss of all modalities below lesion
- Plantars - extensor response bilaterally
- Breathing - not affected
- Remember spinal shock and sphincter disturbance
3
Q
Cauda equina syndrome
A
- Most commonly results from lumbar disc herniation
- Can result from trauma, epidural haematoma, infection or tumour
- Presents with:
- Lower back pain
- Saddle and/or genital sensory disturbance
- Bladder/bowel/sexual dysfunction
- Motor - flaccid paraparesis
- Reflexes - lower limb reflexes absent
- Sensory - saddle anaesthesia, lower limbs - variable sensory deficit
- Plantars - flexor response
4
Q
Brown-Sequard syndrome
A
- Hemi-section of the cord
- Affects LCT, DC and LST
- Can result from trauma, degenerative disease, inflammation, infection or tumour
- Motor - ipsilateral spastic hemi-/mono-paresis
- Reflexes - ipsilateral brisk reflexes
- Sensory - loss of light tough, vibration and proprioception on ipsilateral side; loss of pain and temperature on contralateral side
- Plantars - ipsilateral extensor response
- Breathing - hemi-diaphragmatic weakness in high cervical cord lesions only
5
Q
Posterior column pathology
A
- Some pathologies selectively affect posterior columns:
- Vitamin B12 deficiency
- Tabes dorsalis
- Vitamin E deficiency
- Friedreich’s ataxia
- Clinical presentation:
- Loss of vibration and proprioception
- Sensory ataxia
- Positive Romberg sign
6
Q
Anterior horn cell syndromes
A
- Motor neurone disease
- Peak incidence at 60-70 years, men > women
- Clinical presentation
- Asymmetric limb weakness
- Bulbar symptoms
- Subgroup have cognitive impairment (FTD pattern)
- Pathology
- Degeneration of anterior horns of the spinal cord/cranial nerve motor nuclei
- Degeneration of corticospinal/corticobulbar tracts
- Diagnosis clinical but supported by EMG changes
- Denervation in muscles supplied by more than one spinal region
- Examination features
- UMN and LMN signs
- Prognosis
- Mean survival 2-3 years
- Motor - spastic tetraparesis, wasting/fasciculations in tongue/limbs/intrinsic hand muscles +/- bulbar/pseudobulbar weakness
- Reflexes - pathalogically brisk
- Sensory - normal
- Plantars - extensor response
- Breathing - usually unaffected
7
Q
Subacute combined degeneration of the spinal cord (vitamin B12 and E deficiency)
A
- Affects LCT, DC and SCT
- Motor - bilateral spastic paresis, bilateral limb ataxia
- Sensory - bilateral loss of proprioception and vibration sensation
8
Q
Friedrich’s ataxia
A
- Affects LCT, DC and SCT
- Motor - bilateral spastic paresis, bilateral limb ataxia + cerebellar features
- Sensory - bilateral loss of proprioception and vibration sensation
9
Q
Anterior spinal artery occlusion
A
- Affects LCT and LST
- Motor - bilateral spastic paresis
- Sensory - bilateral loss of pain and temperature sensation
10
Q
Syringomyelia
A
- Affects VH and LST
- Motor - flaccid paresis (typically affecting intrinsic hand muscles)
- Sensory - bilateral loss of pain and temperature sensation
11
Q
Neurosyphilis (tabes dorsalis)
A
- Affects DC
- Sensory - loss of proprioception and vibration sensation