Multiple Sclerosis Flashcards

1
Q

What is Multiple Sclerosis?

A

A chronic and progressive condition that involves demyelination of the myelinated neurones in the CNS.

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2
Q

Epidemiology of Multiple Sclerosis (3).

A
  1. Young (20-40).
  2. Women > Men.
  3. Improvement in Pregnancy and Postpartum Period.
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3
Q

Anatomy of Neurones (3).

A
  1. Myelin covers axon of neurones in CNS to help transmit electrical impulses faster.
  2. Schwann cells in the PNS and Oligodendrocytes in the CNS.
  3. MS only affects the CNS - Oligodendrocytes.
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4
Q

Pathophysiology of MS.

A

Inflammation around Myelin and Infiltration of Immune Cells that cause damage to the Myelin.

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5
Q

Pathological Feature of MS.

A

Lesions are disseminated in Time and Space (lesions vary in location over time, affecting different nerves and causing different symptoms).

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6
Q

Aetiology of MS (5).

A

Associations :
1. Multiple Genes.
2. EBV.
3. Low Vitamin D.
4. Smoking.
5. Obesity.

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7
Q

Clinical Features of MS (8).

A
  1. Optic Neuritis (commonest).
  2. CNVI (Abducens) Palsy = Internuclear Ophthalmoplegia and Conjugate Lateral Gaze Disorder.
  3. Focal Weakness.
  4. Focal Sensory Symptoms.
  5. Ataxia.
  6. Lethargy.
  7. Uhthoff’s Phenomenon (Worsening of Vision following a rise in Temperature).
  8. Incontinence, Sexual Dysfunction and Intellectual Deterioration.
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8
Q

What is Intranuclear Ophthalmoplegia?

A

The internuclear nerve fibres connect the cranial nerve nuclei that control eye movements (3, 4 and 6) to co-ordinate eye movements - failure of this.

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9
Q

What is Conjugate Lateral Gaze Disorder?

A

Disordered movement of both eyes when moving to look laterally.

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10
Q

Give 4 examples of focal weakness in MS.

A
  1. Bell’s palsy.
  2. Horner’s Syndrome.
  3. Limb Paralysis.
  4. Incontinence.
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11
Q

Give 4 examples of focal sensory symptoms in MS.

A
  1. Trigeminal Neuralgia.
  2. Numbness.
  3. Paraesthesia (Pins & Needles).
  4. Lhermitte’s Sign.
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12
Q

What is Lhermitte’s sign?

A

An electric shock sensation travelling down the spine and into the limbs when flexing the neck, indicating disease in the cervical spinal cord’s dorsal column (stretching of the demyelinated dorsal column).

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13
Q

Give 2 types of ataxia in MS.

A
  1. Sensory (loss of proprioceptive sense) = Positive Romberg’s Test ad Pseudoathetosis.
  2. Cerebellar.
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14
Q

Presentations of MS Disease (4).

A
  1. Clinically Isolated Syndrome (1st presentation).
  2. Relapsing-Remitting (commonest).
  3. Secondary Progressive (with gait and bladder disorders).
  4. Primary Progressive (commoner in older people).
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15
Q

What is Relapsing-Remitting Disease?

A

Episodes of disease and neurology followed by recovery, with symptoms occurring in different areas.

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16
Q

How can Relapsing-Remitting Disease be further classified (2)?

A
  1. Active / Not Active.
  2. Worsening / Not Worsening.
17
Q

What is Secondary Progressive Disease?

A

Initially Relapsing-Remitting Disease has become a progressive worsening of symptoms with incomplete remissions (symptoms are permanent).

18
Q

What is Primary Progressive Disease?

A

Worsening of disease and neurology from the point of diagnosis without initial relapses and remissions.

19
Q

How can Secondary/Primary Progressive Disease be further classified (2)?

A
  1. Active/Not Active.
  2. Progressing / Not Progressing.
20
Q

Diagnosis & Investigations of Multiple Sclerosis (3).

A
  1. Clinical Diagnosis suggesting lesions that change location over time.
  2. MRI Scan - Typical Lesions.
  3. Lumbar Puncture - Oligoclonal Bands in CSF.
21
Q

MRI Findings in Multiple Sclerosis (3).

A
  1. High-Signal T2 Lesions.
  2. Periventricular Plaques.
  3. Dawson’s Fingers (Hyperintense Lesions Perpendicular to Corpus Callosum).
22
Q

Management of MS (4).

A
  1. Specialist MDT.
  2. Disease Modification.
  3. Treating Relapses.
  4. Symptomatic Treatment.
23
Q

Disease Modification in MS.

A

Disease-Modifying Drugs and Biologic Therapy to induce long-term remission with no evidence of activity.

24
Q

Treating Relapses in MS (2).

A
  1. 1st line : 500mg Oral Prednisolone daily for 5 days.
  2. 2nd line 1g IV Methylprednisolone daily for 3-5 days.
25
Q

Symptomatic Management in MS (6).

A
  1. Exercise.
  2. Neuropathic Pain.
  3. Depression.
  4. Urge Incontinence (Intermittent Self-Catheterisation if Significant Residual Volume or Anticholinergics if not).
  5. Spasticity (Baclofen, Gabapentin, Physiotherapy).
  6. Fatigue - Amantadine.