Spinal Cord Disease Flashcards

1
Q

How does cord compression present?

A

Chronic and Subacute Compression present as Spastic Paraparesis/Tetraparesis, Radicular Pain at Level of Compression and Sensory Loss below level of compression

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2
Q

Features of radicular pain

A

characteristically worse on coughing/straining (Raised ICP); Numbness starts
distally and rises to level of compression; Usually 2-3 Dermatome levels below level of Anatomical compression; Urinary Retention and Constipation might develop

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3
Q

How to approach acute spinal cord compression

A

Acute Spinal Cord Compression is a Medical Emergency; MRI Spine; CXR might show Primary
Tumour or Infection; Surgical exploration might be necessary

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4
Q

What happens if decompression is delayed

A

Cord Damage becomes irreversible; Good prognosis if Benign Tumours or Haematomas removed early

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5
Q

When can radiotherapy be used?

A

Radiotherapy for Cord Malignancy or Compression due to Inoperable Malignant Vertebral Body Disease causing Cord Compression

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6
Q

Causes of Spinal Cord Compression: Disc/Vertebral

A

– (Central Cervical Disc, Thoracic Disc Protrusion);

Compression due to Cervical Spondylotic Myelopathy is the commonest cause of Spastic Paraparesis in the Elderly

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7
Q

Causes of Spinal Cord Compression: trauma

A

Patients with back trauma need to be immobilised

before assessment

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8
Q

Causes of Spinal Cord Compression: Spinal cord tumour

A

Extramedullary Tumours e.g. Meningiomas and Neurofibromas can cause Cord Compression; Gradually
worsens over time; Vertebral Body Destruction by Bony Metastases (e.g. Prostate, Breast) is a common cause as well
o Intramedullary Tumours (e.g. Ependymomas) are less common; Progress slowly;
Sensory disturbances like Syringomyelia might develop
o Spinal Epidural Abscesses would present in a similar manner

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9
Q

Causes of Spinal Cord Compression: TB

A

Spinal TB commonest cause where TB is common; Destruction of Vertebral
Bodies, Disc Spaces, Local Spread of Infection
o Cord Compression and Paraparesis leading to Paralysis = Pott’s Paraplegia

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10
Q

Causes of Spinal Cord Compression: Epidural haemorrhage and Haematoma

A

Rare complication of Anticoagulation, Bleeding
disorders, Trauma, can occur following LP if clotting is abnormal
o Rapidly progressive Cord/Cauda Equina Lesion can develop

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11
Q

Inflammatory Lesions of the Spinal Cord: MS

A
  • Myelopathy evolves over days, often partial recovery follows in weeks/months
  • Can be seen on MRI with Gadolinium Contrast; Cord Swelling and Oedema
  • Multiple Sclerosis is the commonest cause of Spastic Paraparesis in young adults; 1-2 Spinal Segments affected; Part or Entirety of Cord is affected

• Infection – VZV, EBV, HIV, HTLV1/2 (Tropical Spastic Paraparesis), MTb, Syphilis, Lyme disease,
Schistosomiasis or Para infectious Autoimmune Process E.g. Post Viral, Immunisation
• Neuromyelitis Optica (NMO = Devic’s Disease) – AQP4 Autoantibodies leading to Astrocyte
damage in Spinal Cord and Optic Nerves leading to Long Cord Lesions (≥3 Segments) and
Optic Nerve Demyelination

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12
Q

Inflammatory Lesions of the Spinal Cord: Inflammatory disorders

A

• Systemic Inflammatory disorders – SLE, Sjögren’s, Sarcoidosis

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13
Q

Inflammatory Lesions of the Spinal Cord: Infection

A

VZV, EBV, HIV, HTLV1/2 (Tropical Spastic Paraparesis), MTb, Syphilis, Lyme disease,
Schistosomiasis or Para infectious Autoimmune Process E.g. Post Viral, Immunisation

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14
Q

Neuromyelitis Optica

A

(NMO = Devic’s Disease) – AQP4 Autoantibodies leading to Astrocyte damage in Spinal Cord and Optic Nerves leading to Long Cord Lesions (≥3 Segments) and
Optic Nerve Demyelination

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15
Q

How to treat inflammatory lesions of the spinal cord

A

High-dose Steroids, Immunosuppression; Antimicrobial therapy for specific infections

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16
Q

Vascular Disorders of the Spinal Cord: ASA Occlusion

A

Acute Paraplegia, Loss of Spinothalamic Sensation
due to Infarction of the Anterior 2/3rds of the Spinal Cord
o Aortic Atherosclerosis, Dissection, Trauma, Cross Clamping in Surgery, Vasculitis, Emboli, Thrombotic disorders and Severe Hypotension
o Occlusion of the Artery of Adamkiewicz (= Great Radicular Artery, supplies Thoracic ASA) leads to Watershed Infarction typically at T8

17
Q

Vascular Disorders of the Spinal Cord: AVM

A

Rare, difficult to diagnose but potential curable; Acquired or Congenital (True AVMs)
o Dural AV Fistulas (Acquired) – Occur in Middle-aged Men; Formed due to connection
between Artery and Vein in Dural Nerve Root Sleeve
o Oedema and Congestion at and below affected level; Gradually Progressive
Myelopathy often with Back Pain; MRI shows Cord Swelling, may show enlarged
Arterialised veins

18
Q

Hereditary Spastic Paraparesis

A

– Severe Genetic disorders might present with UMN
syndrome resembling Myelopathy; Spasticity and Stiffness > Weakness
o 28 Genes associated with HSP; Muscle Relaxants (e.g. Baclofen) can improve gait
o Adrenoleucodystrophy – Slowly progressive Spastic Paraparesis

19
Q

Vitamin B12 deficiency

A

Subacute Degeneration of the Spinal Cord; Abuse of Nitric Oxide can precipitate Functional Deficiency even with normal Serum B12

20
Q

Other disorders of the spinal cord

A
  • Motor Neurone Disease – Spastic Paraparesis before LMN signs develop
  • Paraneoplastic Disorders, Radiotherapy, Copper Deficiency, Liver Failure and Toxins
21
Q

Management of Paraplegic Patients: Bladder

A

Does not empty resulting in Urinary Retention; Intermittent Self-Catheterisation or
develop Reflex Bladder Emptying helped by abdominal pressure
o Early treatment of UTI essential; Reflux Nephropathy results in CKD

22
Q

Management of Paraplegic Patients: Bowel

A

Constipation and Impaction must be avoided; Manual Evacuation is necessary; Reflex
emptying develops later

23
Q

Management of Paraplegic Patients: Skin

A

Pressure Ulcer Prophylaxis

24
Q

Management of Paraplegic Patients: Physio and Rehab

A

Wheelchairs, Psychological, Practical needs etc

25
Q

Syringomyelia

A

Syrinx – Fluid-filled Cavity within Spinal Cord; Syringobulbia –
Cavity in the brainstem
Associated with Arnold-Chiari Malformation; Pulsatile waves
of CSF transmitted to fragile tissues of the Spinal Cord
causing Secondary Cavity formation
Syrinx formation might also follow Spinal Cord Trauma; Also by Intrinsic Cord Tumours

26
Q

Consequences of Syringomyelia

A

Expanding Cavity in cord gradually destroys Spinothalamic Neurons, Anterior Horn cells, Lateral Corticospinal Tracts; In the Medulla it will affect Lower
CN Nuclei

27
Q

Management of syringomyelia

A

MRI demonstrates cavity/Herniation in Arnold-Chiari Malformation; Surgical Decompression
of Foramen Magnum causes Syrinx to collapse

28
Q

Presentation of Syringomyelia

A
  • Arnold-Chiari Malformation typically presents 20-30yrs; Upper Limb Pain exacerbating by Coughing/Exacerbation is typical
  • Spinothalamic Sensory Loss (Painless Upper Limb Burns, Trophic Changes) and Paraparesis
  • Suspended Area of Dissociated Sensory Loss (Dorsal Columns Modalities preserved)
  • Loss of Upper Limb Reflexes, Muscle Wasting; Spastic Paraparesis might initially be mild
  • Brainstem – Tongue Atrophy, Fasciculation, Bulbar Palsies, Horner’s Syndrome, Impaired Facial Sensation