Peripheral Neuropathies Flashcards

(62 cards)

1
Q

Examples of pain/temp small fiber pathologies

A

DM
Leprosy
amyloidosis

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2
Q

Examples of proprioception/vibration fiber pathologies

A

Vit B12 deficiency
DM
Hereditable

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3
Q

Examples of motor fiber pathologies

A

Immune-related (Guillan-Barre)
Lead toxicity
Acute intermittent porphyria
Inherited disorders

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4
Q

Examples of autonomic fiber pathologies

A
Amyloid
DM
Sjogren's
Botulism
Amiodarone
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5
Q

Sx and PE of pain/temp fiber damage

A

pain, burning, shock-like, stabbing, dysesthesias, allodynia, paresthesias

PE: decreased response to painful stimuli (pin prick), decreased temp sensation (light touch)

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6
Q

Sx and PE of proprioception/vibration fiber damage

A

numbness, pins & needles, poor balance

PE: decreased proprioception and vibration (joint position sense); diminished DTRs

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7
Q

Sx and PE of motor fiber damage

A

cramps, weak grip, foot drop, fasciculations

PE: weakness, diminished DTRs

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8
Q

Autonomic nerve damage sx and PE

A

lightheaded, dry eyes/mouth, abnormal sweating, erectile dysfxn

PE: orthostasis, anisocoria (unequal pupils)

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9
Q

Location of peripheral neuropathies

A

outside brain and spinal cord

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10
Q

Which cranial nerves are involved in peripheral neuropathy?

A

all cranial nerves except I and II

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11
Q

Most common causes in U.S.? worldwide?

A

US: DM and alcohol
worldwide: leprosy

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12
Q

Most common presentation of peripheral neuropathy?

A

distal symmetric sensorimotor dysfxn

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13
Q

How are PN categorized by pattern of involvement?

A
  • mononeuropathy = single nerve and its innervation
  • Multiple mononeuropathy = multiple indiv peripheral nerves
  • Polyneuropathy = widespread distribution

symmetric vs asymmetric, distal vs proximal

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14
Q

Likely cause of mononeuropathy

A

compression, trauma, vascular cause

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15
Q

common distribution of polyneuropathies

A

“stocking-glove distribution”

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16
Q

How are PN categorized by time course?

A

acute: toxic or inflamm
subacute: chemo, lead
chronic: DM, Charcott-Marie-Tooth
recurrent: Guillan-Barre, HIV

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17
Q

How are PN categorized?

A

Location
Time course
Fiber type
Axonal or Demyelinating

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18
Q

Common example of demyelinating disease

A

MS

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19
Q

axonal neuropathy

A

neuropathy with axonal and myelin sheath degeneration DISTAL to injury (Wallerian degeneration)

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20
Q

Common mononeuropathies

A

median neuritis, radial neuritis, ulnar neuritis, peroneal neuritis

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21
Q

Hypothesis for why so many diabetics get neuropathy?

A

direct axonal loss and demyelination secondary to hyperglycemia OR insufficient blood flow in vaso nervorium

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22
Q

Most common diabetic neuropathy

A

diabetic sensorimotor polyneuropathy (DSPN)

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23
Q

Complications of diabetic neuropathy

A

foot ulcers, Charcot joint

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24
Q

Where nerve fibers affected in DSPN?

A

mixed with small and large fibers, sensory, motor, and autonomic

sensory and autonomic&raquo_space; motor

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25
symptoms of DSPN
initially distal: numbness/tingling, burning of toes/feet progresses to proximal: up leg and to hands ("stocking-glove") later: gait disturbances, distal motor weakness
26
PE of diabetic neuropathy
Distal sensory loss of pain, temp, touch, vibration Reduced DTRs at ankle
27
What are signs of autonomic fiber involvement?
impotence, nocturnal diarrhea, difficulty voiding, abnormal sweating, orthostatic hypotension
28
Asymmetric Diabetic Neuropathy
- occurs in older puts who already have DSPN - involves CN VI, III, and sometimes IV (abrupt onset d/t acute ischemia) - radiculopathies, limb mononeuropathies
29
CN VI palsy affects on vision
painless double vision (diplopia)
30
Tx of diabetic neuropathy
- Strict glycemic control - Tricyclics or gabapentin for pain - Most recover over months
31
"length dependent" neuropathy
longest nerves affected first
32
How is asymmetric diabetic neuropathy different from typical DSPN?
Asymmetric Acute Cranial nerves affected
33
Cause of asymmetric diabetic neuropathy
acute ischemia
34
signs/sx and tx of uremic neuropathy
- Distal symmetric sensoriomotor polyneuropathy - stocking-glove distributions, distal motor weakness, restless leg syndrome - tx: dialysis, renal transplant
35
Examples of infection related neuropathies
``` Bell's Palsy Lyme Disease Herpes Zoster (shingles) Cytomegalic Virus (CMV) in HIV Symmetric Distal Polyneuropathy associated with AIDS ```
36
Bell's Palsy is paresis of _____ nerve and associated with _____ infection.
``` CN VII (facial) herpes simplex virus ```
37
How would Bell's Palsy be classified?
acute mononeuropathy
38
How do you differentiate Bell's Palsy from stroke?
Stroke patient can still wrinkle forehead, only lower face affected Bell's Palsy affects upper and lower face
39
Signs/Sx of Bell's Palsy
UNILATERAL paresis corner of mouth droops, no nasolabial fold, forehead unfurrowed, can't close eyelids SENSORY INTACT
40
Bell's Palsy management
80% recover within weeks to months w/ or w/o treatment May give steroids or Acyclovir
41
Ramsay Hunt Syndrome
may present as Bell's Palsy; so must rule Ramsay out!!! shingles of CN VII with vesicular rash in external canal/pharynx
42
shingles caused by what virus?
Herpes Zoster in adults
43
signs of shingles?
vesicular painful rash in dermatomal distribution
44
Postherpetic neuralgia
persistent pain following shingles that can last years
45
Shingles treatment
Tricyclics Gabapentin Pain meds
46
Lyme disease caused by what organism?
Borrelia burgdoferi in ticks
47
CMV infections often associated with ______.
HIV/AIDS
48
All dying from AIDS with have what neuropathy?
symmetric distal polyneuropathy
49
Different causes of toxic neuropathies
drugs (chemo), heavy metals (lead), industrial compounds, alcohol
50
Chelation therapy
used to treat heavy metal toxic neuropathy
51
______ to prevent and treat isoniazid (INH) neurotoxicity.
pyridoxine (B6)
52
Vitamin deficiencies that result in neuropathies?
Thiamine B1, Pyridoxine B6, Vit B12, Vit E
53
Most common inherited neuromuscular disease that is also an inherited neuropathy
Charcot Marie-Tooth
54
Categorization of Charcot Marie-Tooth
Chronic distal sensory and motor neuropathy which develops over years
55
Signs/Sx of Charcot Marie-Tooth
long standing gait difficulties, h/o being "unathletic" child; mostly LE but progresses hands PE: wasted leg muscles, weakness, hammer toes, distal sensory loss and loss of DTRs
56
Autoimmune acute inflammatory demyelinating polyneuropathy
Guillan-Barre Syndrome
57
Clinical signs of Guillan-Barre Syndrome
* Rapidly evolving motor paralysis with areflexia * Ascending paralysis over hrs to days * C/O "rubbery legs" * DTRs disappear in days * Autonomic instability
58
CSF findings of Guillan-Barre Syndrome
typically normal at disease presentation; after 7-14 days- elevated protein, normal glucose, no pleocytosis
59
Guillan-Barre Syndrome management
85% achieve full recovery within several months to a year; treat ASAP tx: plasmapheresis or IV immune globulins supportive: 30% need intubation, trach, or mechanical ventilation
60
Symptoms of trigeminal neuralgia
- episodes of electric (lancinating) shock pain in CN V innervation - pain so intense they wince ("tic") - single jabs or cluster of pain in "trigger zone" - no sensory loss
61
Who is most likely to be affected by trigeminal neuralgia?
F > M | middle aged/elderly
62
Trigeminal neuralgia treatment
Carbamazepine or phenytoin Surgery if fail med therapy