What are the main categories of spinal cord compression causes?
Extradural, intradural extramedullary, and intradural intramedullary.
What are common extradural causes of spinal cord compression
Tumours (metastases, primary bone tumours)
• Infections (TB, pyogenic, parasitic)
• Disc herniation
• Trauma
What are common intradural extramedullary causes of spinal cord compression?
What are common intradural intramedullary causes of spinal cord compression?
Tumours (astrocytoma, ependymoma, haemangioblastoma)
• Syrinx
• Trauma (cord contusion, acute haematomyelia)
• Inclusions
What are the most common secondary (metastatic) tumours causing spinal compression in adults?
Lung, breast, prostate, thyroid, kidney, melanoma, lymphoma, and leukaemia.
What are the most common secondary (metastatic) tumours causing spinal compression in children?
Neuroblastoma and nephroblastoma (Wilms tumour).
What factors influence the pathophysiology of spinal cord compression?
What types of pain can occur in spinal cord compression?
Local pain (at the level of lesion)
• Radicular pain (nerve root involvement)
• Central pain (cord itself).
What types of weakness are seen in spinal cord compression?
Weakness of lower and/or upper limbs, depending on the level of compression.
Which sensory modalities are commonly disturbed in spinal cord compression?
Spinothalamic tract (pain and temperature)
• Dorsal columns (light touch, vibration, proprioception).
How is sphincter function affected in spinal cord compression?
Bladder involvement: UMN or LMN type dysfunction
• Rectum: impaired control or constipation depending on level/type of injury.
What upper motor neuron (UMN) signs are seen in spinal cord compression?
Spasticity, hyperreflexia, clonus, and positive Babinski sign (extensor plantar response)
What lower motor neuron (LMN) signs may be present in spinal cord compression?
Flaccid paralysis, muscle wasting, fasciculations, and hyporeflexia/areflexia (at the level of lesion).
What sensory signs are seen in spinal cord compression?
Loss of pain, temperature, touch, vibration, or proprioception depending on which tracts are affected (spinothalamic vs dorsal column), often with a sensory level.
What is transverse cord syndrome?
Complete loss of motor, sensory, and autonomic function below the lesion, often due to trauma, infarction, or transverse myelitis.
What is posterior cord syndrome
Loss of light touch, vibration, and proprioception (dorsal columns), with preserved motor and pain/temperature. Often due to B12 deficiency or tabes dorsalis.
What is Brown-Séquard syndrome?
Ipsilateral motor weakness and loss of proprioception, with contralateral pain and temperature loss. Typically due to penetrating trauma or tumours.
What is central cord syndrome?
Cape-like loss of pain and temperature across shoulders/arms, LMN weakness at lesion level (hand wasting), and UMN spasticity below. Causes: syringomyelia, trauma, tumours.
What is anterior cord syndrome?
Loss of motor, pain, and temperature below the lesion, with preserved light touch and proprioception. Causes: anterior spinal artery thrombosis, trauma, disc prolapse.
How does conus medullaris syndrome present?
Symmetrical lower limb weakness, early bladder/bowel dysfunction, mixed UMN + LMN signs, and saddle anaesthesia.
How does cauda equina syndrome present?
Asymmetrical lower limb weakness, radicular pain, areflexia, late bladder/bowel involvement, and saddle anaesthesia.
What basic imaging investigations are used in spinal cord compression?
X-ray, MRI (gold standard), myelogram, CT scan, and isotope bone scan.
Which blood tests are useful in spinal cord compression evaluation?
FBC, ESR, and serum electrophoresis (to look for malignancy, infection, or inflammation).
Which urine test is important in suspected malignant spinal cord compression?
Urine for Bence-Jones proteins, which indicate malignant B-cell proliferation (e.g., multiple myeloma).