peripheral neuropathy Flashcards

1
Q

symptoms?

A

• Sensory: numbness, tingling, “pins and
needles”, pain, cramps

• Motor: weakness, wasting, difficulty
walking, unsteady
Symptoms tend to start in the feet

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2
Q

signs?

A
  • Tone: normal
  • Power: distal weakness +/- wasting

• Reflexes: depressed or absent
(AJ before KJ)

  • Sensation: “sock +/- glove” distribution
  • Gait: normal/ataxic/foot drop
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3
Q

common causes

A

• Diabetes mellitus
• Alcohol/drugs
• Inflammation
• Inherited
• Others: cancer, infection (leprosy, HIV,
Lyme disease)

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4
Q

investigations?

A

• Glucose
• FBC, ESR, U&E, LFTs, thyroid function,
B12, autoimmune screen,
serum protein electrophoresis
• Nerve conduction studies:
Normal : 50-60 m/s
Axonal: 37-40 m/s
Demyelinating: 5-36 m/s

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5
Q

case 1.

• 49y/o man
• Diabetic for 15 years. Modest control
• 12 months of tingling and numbness in his feet
6 months of burning and shooting
pains in his feet – worse at night, causing
insomnia and depression
Examination: normal strength
absent ankle jerks
impaired vibration/PP/LT to mid shin

A

• Sensory; axonal
• Commonest symptoms:
pains, pins and needles, numbness
• Signs:
absent ankle jerks
“sock” pattern of sensory loss

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6
Q

case 1 treatment

A
  • Maintain good blood glucose control
  • Foot care
  • Pain relief
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7
Q

examination of someone with guillian barre syndrome?

A

Examination
• Mild bilateral facial weakness
• Global arm and leg weakness dist>prox
• Absent reflexes
• Mild glove and stocking sensory loss
• Could just stand/walk with support

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8
Q

patology of guillian barre?

A

• Motor; demyelinating
• Incidence: 2 in100,000 population
• Develops after an infection (eg campylobacter)
• Progresses over 4 weeks to
(i) limb paralysis
(ii) cranial nerve problem
(iii) respiratory muscle weakness
(iv) autonomic dysfunction

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9
Q

treamtne of GB syndrome?

A

• Ascending paralysis can lead to weakness
of the diaphragm and chest wall muscles
• Cardiac arrhythmias
Treatment: intravenous immunoglobulin
plasma exchange
ventilatory support
cardiac monitor

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10
Q

history of charcot marie tooth syndrome patient?

A

24y/o man referred because of problems
walking going back 6 months
• Problems running as a child
• Always had funny shaped feet
• His sister had odd feet as did his mother

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11
Q

foot drop also called?

A

pes cavus

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12
Q

CMT may posses?

A

small hands

claw hands (fingers drawn inwords)

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13
Q

pathology of CMT?

A

• Sensori-motor; axonal or demyelinating
• Autosomal dominant inheritance
• Begins early in life and so associated with
foot deformities (pes cavus), clawed toes
difficulties walking/running
• Affects 1 in 2500

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14
Q

peripheral myelin protein 22?

A

• Chromosome 17 – short arm is duplicated
• Gene for Peripheral Myelin Protein 22Kd
(PMP 22) is on short arm
• Test +ve in 70% of cases
CMT 1: demyelinating, PMP22 duplication
CMT 2: axonal. No gene marker to date

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15
Q
A
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