Myelopathy Flashcards

1
Q

What is the classification of myelopathy?

A
COMPRESSIVE
V - AVM, hematoma
I - abscess, tuberculoma
N - tumors 
D - Atlanto-axial instability
       Osteophytes
       Central disc herniation 
C - syringomyelia/ chiari malformation
T - trauma

NON COMPRESSIVE

V - anterior spinal artery thrombosis
I - transverse myelitis, vasculitis (SLE)
N - vitamin B12 deficiency
D - multiple sclerosis, MND, syringomyelia
I - HIV , syphilis

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2
Q

What is non compressive myelopathy?

A

Pathologic conditions

That are not the result of mass pressure effects

Which cause damage and/ or dysfunction

To the spinal cord
Spinal meninges
Or perimeningeal spaces

Leading to sensory, motor and bladder-bowel dysfunction

*non compressive myelopathy must only be considered after performing imaging to rule out compressive aetiologies

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3
Q

What is transverse myelitis?

A

Non compressive myelopathy

Due to acute inflammation of the spinal cord

Restricted to few segments

Leading to loss of motor, sensory and sphincter function below the lesion

Which develop over few hours

Caused by idiopathic, infectious and post-infectious conditions

1/3rd are left with serious disability

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4
Q

How do you diagnose transverse myelitis?

A

Clinical criteria

  • exclude compressive lesion by MRI
  • sensory, motor and autonomic dysfunction
  • Bilateral signs and symptoms
  • clearly defined sensory level
  • progressive over hours

Investigation criteria demonstrating spinal cord inflammation

  • CSF pleocytosis or high IgG
  • gadolinium MRI for inflammation
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5
Q

What are the spinal cord syndromes?

A

Spinal shock syndrome

Complete cord transection syndrome

Anterior cord syndrome

Central cord syndrome

Brown-Sequard syndrome

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6
Q

What are the features of anterior cord syndrome from vascular infarction?

A

Below the segment

Acute flaccid hemiparalysis 
Sensory level for PTT
Sparing of JPS and V
Sphincter dysfunction
Absent anal reflex

AFTER SPINAL SCHOK

#At the segment
Bilateral LMN signs

Bilateral UMN signs
Bilateral sensory loss

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7
Q

What is subacute combined degeneration of the cord (SCDC)?

A

A dorsolateral spinal cord syndrome

Caused by demyelination and degeneration of the posterior and lateral white matter tracts

Following vitamin B12 deficiency

Presenting with combined UMN LMN signs
Subacute slowly progressive 
Paresthesia of the extremities
Weakness and numbness
Sensory ataxia

Spasticity
Paraplegia
Incontinence

On examination
KJ hyper reflexia
ABSENT AJ reflex 
Extensor plantars 
Stocking sensory loss
Loss of JPS
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8
Q

What are the causes for absent ankle jerks with extensor plantars?

A
SCDC
MND
Tabes dorsalis 
Friedrich ‘s ataxia
Conus medullaris syndrome
Combined pathology (cervical spondylosis plus peripheral neuropathy)
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9
Q

What are the features of central cord syndrome?

A

After spinal shock

Bilateral LMN signs in segments affected

Bilateral UMN signs below the lesion with sacral sparing (upper limb>lower limb)

Bilateral sensory loss below the lesion with sacral sparing (upper limb>lower limb)

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10
Q

What are the features of Brown-Séquard syndrome?

A

After spinal shock

Ipsilateral LMN signs in the hemisegment

Ipsilateral UMN signs below the lesion

Ipsilateral anesthetic band in the hemisegment

Ipsilateral loss of dorsal column signs below lesion

Contralateral spinothalamic signs below the lesion

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