multiple sclerosis Flashcards

1
Q

what are the types of MS

A

relapsing remitting MS, secondary progressive MS, primary progressive MS

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2
Q

what is the pattern in RRMS

A

typically onset over days, recover over weeks

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3
Q

what happens in secondary progressive

A

gradually worsening disability over years. 75% of RRMS patients evolve into secondary progressive

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4
Q

what happens in primary progressive

A

gradually worsening disability with no relapses or remissions. later in onset and less inflammatory changes on MRI

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5
Q

what are the three characteristic presentations of MS

A

optic neuritis, brainstem demyelination, spinal cord lesions

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6
Q

symptoms of optic neuritis

A

visual loss, mild fogging of central vision, central scotoma, painful eye movements

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7
Q

symptoms of brainstem demyelination

A

diplopia, vertigo, nystagmus, dysarthria, dysphagia

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8
Q

what is pathognomonic for MS

A

blateral internuclear ophthalmoplegia (INO)- disorder of conjugate lateral gaze so affected eye cant adduct

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9
Q

signs of spinal cord lesions

A

paraparesis that develops over days/weeks, difficulty walking and limb numbing often asymmetric. Lhermittes sign. arms affected if high cervical cord lesion, tight band sensation around abdomen and chest if thoracic lesion

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10
Q

what is Lhermittes sign

A

electric like sensation down the trunk and limbs on neck flexion

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11
Q

what is Unthoffs phenomenon

A

worsening of pre existing symptoms with increase in body temperature eg after exercise or taking a hot bath

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12
Q

common symptoms

A

visual changes, sensory disturbances- abnormal sensation 40% presenting complaint- reduced vibration sense and JPS, clumsy/useless hand due to loss of proprioception, ataxic/unsteady, neuropathic pain, fatigue, urinary frequency and urgency, spasticity- baclofen, temperature sensitivity (Unthoffs)

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13
Q

what is a rare but pathognomonic presentation

A

tonic spasms- frequent brief spasms of one limb

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14
Q

diagnosis of MS

A

> 2 attacks affecting different parts of the CNS. disseminated in time and space

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15
Q

what criteria is used in the diagnosis of MS

A

McDonald criteria

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16
Q

what is required in investigations of MS and what is the main investigation

A

evidence of dissemination in time and space. MRI is the main investigation

17
Q

what could the MRI show

A

multiple scattered lesions showing dissemination through space.

18
Q

why can the MRI not be the most effective investigation

A

in patients >50 small ischaemic lesions cant be distinguished and in younger patients those with neuro inflammatory disorders eg sarcoidosi, Bechets, vasculitis

19
Q

what other investigations can be used

A

cord imaging, CSF- oligoclonal IgG bands (not specific), evoked responses, blood tests to exclude other inflammatory disorders

20
Q

treatment of acute relapse of MS

A

short course of steorids eg IV methylprednisolone 1g/day for 3 days or high dose oral steroids

21
Q

treatment MS

A

disease modifying drugs for RRMS- immunomodulatory- B interferon or glatiramer acetate reduce relapse by 1/3 in RRMS and up to half in serious relapses.

22
Q

when are disease modifying drugs given to patients

A

if the patient is ambulatory and has had 2 or more significant attacks in 2 years or one serious attack

23
Q

what can be added into the treatment of aggressive RRMS

A

monoclonal antibodies eg natalizumab

24
Q

what are poor prognostic factors

A

high MR lesion load at diagnosis, high relapse rate, male gender and late presentation