Peripheral Neuropathy Flashcards

1
Q

list 5 conditions associated with carpal tunnel syndrome

A

1) hypothyroidism
2) pregnancy in the third trimester
3) rheumatoid disease
4) acromegaly
5) amyloid (inc in dialysis patients)

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2
Q

treatment of MG

A

acetylcholine esterase inhibitors (pyridostigmine)
IV Ig plasma exchange
Immunosuppressants

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3
Q

name 3 autoimmune disorders of the nueromusclar junction

A

LEMS
neuromyotonia
Myasthenia Gravis

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4
Q

Lambert Eaton Myasthenic syndrome is associated with which type of cancer

A

60% is associated with small cell lung cancer and infact may precede diagnosis by 4 years

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5
Q

presentation of LEMS

A

very rare
causes hyporeflexia and weakness that can be transiently imroved through exercise
caused by antibodies against voltage gated calcium channels

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6
Q

presentation of neuromyotonia

A
very rare
hypertonic stiffness in muscles
cramps
myokymia
caused by antibodies against voltage gated potassium channel which prevents the swithc off of ACh release
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7
Q

presentation of myasthenia gravis

A

uncommon
fatiguable weakness
EYE - diplopia and weakness of eye closure
BULBAR - speech swallowing chewing difficulty smiling
NECK- extension weakness
proximal limb muscle weakness
caused by antibodies against around 80% ACh receptors preventing adequate end plate potentials

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8
Q

what is early onset myasthenia graves associated wtih

A
young women (menarche - 40)
Thymic hyperplasia
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9
Q

what is later onset MG associated with

A

older men

atrophic thymus

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10
Q

which tumour is myasthenia graves associated wtih

A

thymoma at any age

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11
Q

sensory signs of nerve dysfunction

A
numbness 
buring
ataxia
allodynia
reduced proprioception
areflexia
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12
Q

motor signs of dysfunction

A

weakness
wasting
fasciulation
areflexia

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13
Q

what is mononeuropathy multiplex

A

nerve damage involving one or more nerve trunks
usually asymmetrical
(eg in diabetes, leprosy, vasculitis)

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14
Q

what is Wallerian degeneration

A

degeneration of nerve fibres distal to axon separation from cell body

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15
Q

what is poly neuropathy

A

neuropathy involving multiple nerve trunks
symmetrical and usually starts distally

eg GBS sock and glove

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16
Q

what is mononeuropathy

A

single nerve involvement from a local cause

eg trauma or compression

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17
Q

what is neuropathy

A

a pathological process that damages a nerve producing signs and symptoms

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18
Q

symptoms of axonal degeneration

A

tingling
burning
weakness
loss of motor function

19
Q

give examples of acute and chronic demyelinating neuropathies

A

acute- GBS

chronic - Chronic inflammatory demyelinating polyneuropathy

20
Q

first presentation of GBS

A

sock and glove neuropathy

21
Q

Treatment of GBS

A
IV Ig (decreases duration)
plasma exchange (eliminate pathogen)
supportive care
22
Q

most common precursor to GBS

A

Campylobacter pylori

23
Q

presentation of peripheral neuropathy

A
tingling
numbness of digits
weakness of limbs
hyporeflexia
fatigue
abnormal sensation
24
Q

3 causes of axonal degeneration

A

diabetes
alcoholism
genetics (CMT, leprosy)

25
what is Charcot Marie Tooth syndrome
a genetic condition where axonal degeneration is caused by multiple gene mutations for proteins in myelin schwann cells and axons
26
name an anaesthetic which works by blocking sodium channels
lidocaine
27
name an anticonvulsant which works by using sodium channels
carbamezine
28
name 3 excitatory neurotransmitters
noradrenaline - used in the Symp ANS adrenaline - NA agonist Acetylcholine - post ganglionic para NS and in motor end plates
29
signs and symptoms of autonomic neuropathy
``` dry mouth/eyes syncope GI disturbance bladder urgency/frequency impotence dry skin and excessive/inadequate sweating pupil constriction ```
30
what is "dying back" neuropathy
distal axonal degeneration often due to toxic/metabolic abnormalities of neuronal cell body (HIV/AIDS; alcohol etc) starts peripherally and dies back towards the cell body
31
aetiologies of chronic peripheral neuropathy
variable: - idiopathic - diabetes/impaired glucose tolerance - drugs (statins, cytotoxic drugs) - B12 deficiency - alcohol - inherited
32
presentation of radial nerve compression neuropathy
wrist drop and weakness of brachoradialis
33
presentation of ulnar nerve compression at the elbow
hypothenar wasting weakness of finger abduction and opposition of little finger sensory changes in medial 1.5 fingers
34
presentation of carpal tunnel syndrome
numbness in lateral digits waking at night weakness of thumb abduction wasting of thinner eminence
35
presentation of malaria parasthetica
numbness/burning over anterolateral thigh following sudden increase in weight, surgery or injury
36
presentation of compression neuropathy of the common perennial nerve around the fibula
foot drop and weakness of ankle eversion with preserved ankle jerk numbness on anterolateral dormer of the dorsum of the foot follows prolonged sitting/bed rest
37
features of CIDP
- slow onset and recovery - progressive/relapsing procimal and distal limbe weakness and sensory loss - CSF protein raised (>0.4)
38
thiamine deficiency causes which syndrome
Wernicke-Korsakoff - abnormal eye movements (nystagmus, bilateral L rectus palsy, conjugate gaze palsies) - ataxia (broad based gait, cerebellum signs and vestibular paralysis) - cognitive change (acute stupor/coma followed by amnesic syndrome and confabulations)
39
which vitamin deficiency neuropathy presents as: tingling and numbness of fingers and toes distal sensory loss (esp in dorsal column) absent ankle jerks exaggerated knee jerks and extensor plantear response
B12 Cobalamin
40
what are the causes of peripheral neuropathy
``` Diabetes Alcoholism Vitamin deficiency Infective/inherited Drugs (e.g. isoniazid) ```
41
name 6 methods of peripheral nerve damage
demyelination axonal degeneration (usually toxic neuropathies) wallerian degeneration (crush injuries) compression infarction (polyarteritis nodosa, Churg-Strauss) infiltration (leprosy, malignancy, inflammation, sarcoidosis)
42
mixed upper and lower motor neurone signs is indicative of which group of conditions
motor neurone disease 75% have symmetrical weakness and wasting usually painless 25% bulbar and pseudo bulbar features (eye movements usually spared) there is NO sensory loss sphincters are NOT affected
43
which tracts are affected by ALS
lateral corticospinal tracts causing a spastic paraparesis