Neuro 2 Flashcards

spinal cord stuff neurofibromatosis

1
Q

Central cord syndrome (syrinx)

  • mechanism of injury
  • presentation
  • diagnosis?
  • Rx?
A
  • forceful hyperextension of spondylotic neck
  • loss of sensor and motor function upper body&raquo_space;> lower body- typically in ‘shawl’ region
  • MRI spine
  • neurosurgical intervention
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2
Q

Brown-Sequard syndrome

  • mechanism f injury
  • presentation
A

hemicord lesion

  • knife/bullet injury or MS
  • lose ipsilateral soft touch/propioception and weakness AND contralateral loss of pain and temp
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3
Q

Anterior cord syndrome

  • mechanism of injury
  • clin features
A

involves tracts in anterior two- thirds of spinal cord

  • compression injury or vascular
  • complete loss of motor,pain and temp below injury but retains propioception and vibration
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4
Q

Cauda equina syndrome

  • aetiology
  • clin features
  • Rx
A
  • disc herniation, lumbar stenosis
  • bilateral leg weakness, bladder and rectal incontinence, ,asymmetrical multiradicular pain
  • dexamethason and surgical decompression
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5
Q

Lumbar spinal stenosis

  • causes
  • symptoms
  • best inv
  • treatment
A
  • usually degenerative joint disease
  • pain worse with back extension (walking downhill), unilateral leg pain and weakness
  • MRI
  • NSAIDs and physio (same as OA)
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6
Q

Syringomyelia

  • usual site affected
  • clin features
  • associations?
A

cysts in spinal cord usually C8/T1

  • intrinsic muscle weakness and loss of spinothalamic function
  • chiari malformation
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7
Q

Guillian Barre syndrome

  • define
  • associations
A

acute demyelinating disease including peripheral and cranial nerves
most commonly associated with C. jejuni (can be any bacteria or virus)

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8
Q

Signs and symptoms of GBS

A
symmetrical ascending weakness
areflexia
autonomic dysfunction
- bilateral Bell's palsy
- reduced distal propioception and vibration
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9
Q

what is the miller-fisher variant of GBS?

A

like GBS but presents with opthalmoplegia, areflexia and ataxia

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10
Q

investigations and treatment of GBS

A

Ix: MRI
lumbar puncture: raised protein
Rx: IV Ig- takes wks-months to recover

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11
Q

CIDP

  • define
  • clin features
A

inflammation of the nerve roots and peripheral nerves with destruction of the myelin sheath
- symmetrical weakness of hip and shoulder muscles with impaired motor and sensory function, areflexia

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12
Q

CIDP

  • inv
  • treatment
A
  • nerve conduction tests, lumbar puncture (raised protein), MRI
  • iv Ig and steroids
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13
Q

Charcot-Marie-Tooth syndrome (HMNS)

  • inheritance
  • clin features
  • management
A
  • AD
  • onset in puberty with thickened enlarged nerves esp common peroneal (foot drop absent ankle jerks)
    symmetrical muscle atrophy and loss of sensation
  • supportive management (physio)
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14
Q

treatment of Bell’s palsy

A

if present within 72 hours give pred

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15
Q

movement disorder presents in <40yrs what is main differential?

A

Wilson’s disease

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16
Q

FIRST line treatment in <55yr old with confirmed Parkinsons

A

Dopamine agonists- ropinorole

17
Q

Multi system atrophy

  • clin features
  • MRI sign
A

most common in late 50s, has autonomic dysfunction and cerebellar ataxia with parkinsonism
- hot cross bun sign

18
Q

Progressive supranuclear palsy

  • clin features
  • MRI sign
A
  • early falls, axial rigidity, vertical eye movements (fast saccades) and dysarthria
  • hummingbird sign
19
Q

features of Essential tremor

A
  • may run in families
  • intention tremor (esp when hold hands out straight)
  • head tremor
  • improves with ETOH
20
Q

what are the 4 types of MND (just name them)

A
  1. ALS (typical)
  2. Progressive muscular atrophy
  3. primary lateral sclerosis
  4. progressive bulbar palsy
21
Q

MND inheritance

A

AD

22
Q

ALS clinical features

A

UMN and LMN signs asymmetrical onset

  • widespread fasciculation (TONGUE)
  • brisk jaw jerk
  • upgoing plantars
23
Q

Progressive muscular atrophy clin features

A

LMN weakness of arms and legs

24
Q

primary lateral sclerosis

clinc features

A
  • symmetrical UMN signs
  • marked spastic leg weakness
  • pseudobulbar palsy (no tongue fasciculations, slow tongue)
25
Q

progressive bulbar palsy clin features

A

CN 9-12 involvement

flaccid and fasciculating tongue with loss of gag reflex

26
Q

Investigations and management of MND

A

inv: usually clinical diagnosis but can use nerve conduction studies, lumbar puncture to rule out MS
- MDT involvement
Riluzole 50mg BD

27
Q

Diagnostic criteria for NF1

A

NEED 2/7

  1. > =6 cafe-au-lait spots must be atleast 5mm wide in children or 15mm in adults
  2. axillary/inguinal freckles
  3. > = 2 neurofibromas
  4. optic nerve glioma
  5. > = iris harmatoma
  6. sphenoid dysplasia/long bone abn
  7. first degree relative with NF1
28
Q

what specific malignant tumours are associated with NF1

A

Phaeos

meningomas

29
Q

How does NF2 classically present

A

presents >20yrs, classically with bilateral acoustic neuroma and bilateral cataracts
- associated with meningomas