more brain stuff Flashcards

Mostly nerve disorders.

1
Q

risk factors for giant cell arteritis

A

polymyalgia
rheumatica
age

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2
Q

pathology of giant cell arteritis

A

inflammation of temporal artery due to granulomatous build up

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3
Q

symptoms of giant cell arteritis

A
claudication of jaw
scalp sensitivity
temple pain 
sudden unilateral blindness 
headache
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4
Q

complications of giant cell arteritis

A

blindness

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5
Q

diagnosis of giant cell arteritis

A

temporal artery biopsy
ESR and CRP up
ACE up

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6
Q

treatment of giant cell arteritis

A

high dose steroid (prednisolone)

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7
Q

risk factors for spinal cord compression

A

osteoporosis
malignancy
slipped disc

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8
Q

treatment of spinal cord compression

A

treat underlying cause

compression relief surgery

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9
Q

diagnosis of spinal cord compression

A

emergency MRI
biopsy
serum electrophoresis
CXR to check for lung cancer

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10
Q

symptoms of a trapped nerve

A

patient feels pain in the distribution of that nerve because the axon spontaneously fires when irritated

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11
Q

lower motor neuron lesion signs

A

signs at the level of the lesion

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12
Q

upper motor neuron signs

A

signs below the level of the lesion

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13
Q

causes of cauda equina syndrome

A

malignancy

disc herniation

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14
Q

signs of cauda equina syndrome

A

mixed UMN and LMN signs
leg weakness
early urinary retention

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15
Q

symptoms of cauda equina syndrome

A

low back pain
pain that radiates down leg
numbness around anus
loss of bowel or bladder control

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16
Q

complications of cauda equina syndrome

A

ongoing bladder/sexual dysfunction

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17
Q

diagnosis of cauda equina syndrome

A

CT/MRI

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18
Q

treatment of cauda equina syndrome

A

surgical relief

laminectomy

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19
Q

risk factors for Brown-Sequard syndrome

A

trauma

septic emboli

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20
Q

pathology of Brown-Sequard syndrome

A

damage to one half of the spinal cord

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21
Q

signs of Brown-Sequard syndrome

A

loss of two point discrimination
ipsilateral UMN weakness
ataxia
ipsilateral Babinski sign

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22
Q

symptoms of Brown-Sequard syndrome

A

ipsilateral paralysis and loss of proprioception

contralateral loss of pain and temperature sensation

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23
Q

diagnosis of Brown-Sequard syndrome

24
Q

risk factors for accessory nerve disorder

A

medical procedures to neck - e.g. cervical lymph node biopsy

25
pathology of accessory nerve disorder
palsy of accessory nerve, leading to sternocleidomastoid and trapezius function loss
26
signs of accessory nerve disorder
loss of muscle mass fasciculations partial paralysis winged scapula
27
symptoms of accessory nerve disorder
muscular weakness in trapezius and sternocleidomastoid
28
treatment of accessory nerve disorder
surgical repositioning of muscles | preservation of C2-4
29
risk factors for Bell's palsy
diabetes | pregnancy
30
pathology of Bell's palsy
CN7 palsy, often as a result of a viral infection
31
signs of Bell's palsy
``` unilateral facial weakness numbness/pain around the ear ageusia (loss of taste) sagging of mouth speech difficulty unable to wrinkle forehead ```
32
complications of Bell's palsy
crocodile tears - unilateral lacrimal stimulation
33
diagnosis of Bell's palsy
rule out brainstem lesion, stroke, tumour | bloods - increased Borrelia antibodies in Lyme disease
34
treatment of Bell's palsy
prednisolone (give quickly)
35
symptoms of third nerve palsy
pupils down and out ptosis diplopia
36
what is the most common mononeuropathy?
carpal tunnel syndrome
37
symptoms of carpal tunnel syndrome
aching in hand and arm (esp. at night) paraesthesia in thumb, index, and middle finger relieved by dangling arm over the bed
38
diagnosis of carpal tunnel syndrome
maximal wrist flexion for one minute can induce symptoms | tapping over the nerve can cause tingling
39
treatment of carpal tunnel syndrome
splinting local steroid injection decompression surgery
40
what percentage of patients over 40 with myasthenia gravis have thyme hyperplasia?
70%
41
what percentage of patients with myasthenia gravis have a thymic tumour?
10% they may have antibodies to striated muscle
42
pathology of myasthenia gravis
autoimmune disease and B and T cell mediation antibodies to nicotinic acetylcholine receptors at neuromuscular junctions some pts have anti-MuSK instead (against tyrosine kinase)
43
signs of myasthenia gravis
ptosis diplopia myasthenia snarl symptoms worse at end of day
44
order of muscle fatigue in myasthenia gravis
``` extraoccular bulbar face neck limb girdle trunk ```
45
complications of myasthenia gravis
myasthenia crisis - weakness of respiratory muscle
46
diagnosis of myasthenia gravis
anti-AChR antibodies in 90% EMG - decreasing muscular response to repetitive nerve stimulation single fibre EMG - block and jitter of orbiculares occuli CT to exclude thymoma tensilon test
47
treatment of myasthenia gravis
``` anti cholinesterase (pyridostigmine) immunosuppresion (prednisolone) plasma pharesis IV immunoglobulin thymectomy ```
48
risk factors for peripheral neuropathies
``` infection ischaemia toxins (e.g. vitamin B6 excess) inflammatory disease hereditary ```
49
characteristics of sensorimotor neuropathy
symmetrical | length dependent
50
characteristics of sensory neuropathy
asymmetrical
51
symptoms of peripheral neuropathy
loss of perception of temperature and pressure loss of balance (ataxia - worse in the dark) muscle cramps muscle weakness fasciculations muscle atrophy
52
what should you always check for in patients presenting with asymmetrical sensorimotor neuropathy?
vasculitis
53
treatment of peripheral neuropathies
amitriptyline, pregabalin, or gabapentin for pain quinine for cramps physiotherapy and walking aids to help with balance
54
risk factors for Guillain-Barre syndrome
Campylobacter infection
55
signs of Guillain-Barre syndrome
rapid ascending paralysis and sensory deficits | GI infection might precede the disease
56
treatment of Guillain-Barre syndrome
IVIG - plasma exchange - do immediately | ITU