Chapter 27: Diseases of Peripheral Nerves Flashcards

1
Q

Which painful nodule composed of non-neoplastic haphazard whorled proliferation of axonal processes and assoc. Schwann cells results from failure of axons to find their distal target during regeneration ?

A

Traumatic neuroma aka “pseudotumor”

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2
Q

What is the electrophysiologic hallmark of axonal neuropathies vs. demyelinating neuropathies?

A
  • Axonal neuropthay = a reduction in signal strength
  • Demyelinating neuropathy = slowed nerve conduction velocity
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3
Q

What are the primary targets of damage in demyelinating neuropathies?

A

Schwann cells w/ their myelin sheaths

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4
Q

Why is the peripheral nerve dysfunction caused by neuronopathies equally likely to affect proximal and distal parts of the body?

A

Damage at the level of neuronal cell body

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5
Q

Mononeuritis multiplex describes a disease process that damages several nerves in a haphazard fashion and is commonly due to what?

A

Vasculitis i.e., polyarteritis nodosum

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6
Q

Characteristic “stocking and glove” distribution of sensory deficits is seen with what anatomic pattern of peripheral neuropathies?

A

Polyneuropathies

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7
Q

Histologic features of Guillain-Barre Syndrome are characterized by what?

A

Inflammation** and **demyelination of spinal nerve roots and peripheral nerves = radiculoneuropathy

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8
Q

2/3’s of Guillain-Barre Syndrome cases are preceded by what; which etiologies have been implicated?

A
  • Acute, influenza-like illness
  • Campylobacter, CMV, EBV, and Mycoplasma penumoniae, or prior vaccination
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9
Q

Morphologically what is the most prominent lesion seen in Guillain-Barre Syndrome?

A

Segmental demyelination affecting peripheral nerves

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10
Q

Clinical presentation of Guillain-Barre Syndrome is dominated by what signs/sx’s; what characteristic CSF finding will there be?

A
  • Ascending paralysis and areflexia
  • DTR’s lost early in the process
  • CSF protein levels w/ little or no CSF pleocytosis (inflammatory cells remain confined to the roots
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11
Q

How is Guillain-Barre Syndrome managed clinically?

A

Plasmapheresis and IV Ig

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12
Q

What is the most common acquired inflammatory peripheral neuropathy?

A

Chronic inflammatory Demyelinating Poly(radiculo)neuropathy

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13
Q

Chronic inflammatory Demyelinating Poly(radiculo)neuropathy is characterized by what type of neuropathy?

A

Symmetrical mixed sensorimotor polyneuropathy that persists for 2 months or more

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14
Q

Which 2 features of Chronic inflammatory Demyelinating Poly(radiculo)neuropathy distinguish it from Guillain-Barre?

A

Time course (presence at least 2 months) and response to steroids

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15
Q

How is Chronic inflammatory Demyelinating Poly(radiculo)neuropathy treated?

A

Glucocorticoids + IVIg + plasmapheresis

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16
Q

Upon sural nerve biopsy in patient with Chronic inflammatory Demyelinating Poly(radiculo)neuropathy what is a characteristic finding?

A

Onion-bulbs: excessive proliferation –> multiple layers of Schwann cells wrap around an axon like the layers of an onion

17
Q

In lepromatous leprosy (Hansen Disease) Schwann cells are invaded by Mycobacterium leprae and what pattern of peripheral nerve damage will be seen?

A

Segmental demyelination and remyelination + loss of both myelinated and unmyelinated axons

18
Q

Which type of neuropathy is seen with lepromatous leprosy (Hansen Disease) and which sensory fibers will be lost?

A
  • Symmetric polyneuropathy affected cool distal extremities and face
  • Involves pain fibers, loss of sensation = injury; since pt’s are rendered unaware of injurious stimuli –> large traumatic ulcers
19
Q

More localized nerve involvement associated with granulomatous nodules in the dermis is characteristic of what form of leprosy?

A

Tuberculoid leprosy = TH1 (cell-mediated) response

20
Q

Peripheral nerve dysfunction as a result of Diptheria is due to what; what are the early sx’s and later findings?

A
  • Result of diptheria exotoxin
  • Early loss of proprioception and vibratory sensation
  • Acute peripheral neuropathy assoc. w/ prominent bulbar and respiratory m. dysf.
21
Q

If VZV is reactivated it travels along sensory nerves and leads to what?

A

Painful, vesicular skin eruption (shingles) in a sensory dermatomal distribution

22
Q

Which dermatomes are commonly affected by VZV reactivation; what kind of damage is seen?

A
  • Thoracic or trigeminal nerve dermatomes
  • Neuronal destruction and loss of affected ganglia
  • Axonal degeneration of periphral nerves after death of sensory neurons
23
Q

Focal destruction of which neuronal structures may be seen with reactivation of VZV?

A

Large motor neurons in anterior horn or cranial nerve nuclei

24
Q

What is the most common pattern of peripheral neuropathy seen with Diabetes?

A

Ascending distal symmetric sensorimotor polyneuropathy

25
Q

Prevalence of peripheral neuropathy associated with diabetes is dependent on what?

A

Duration of the disease

26
Q

Biopsies of the affected peripheral nerves/arterioles in diabetes will show what finding and with what stain?

A

Endoneurial arterioles show thickening, hyalinization, and intense PAS-(+) of their walls + extensive reduplication of basement membranes

27
Q

Diabetic peripheral neuropathy is characterized by a relative loss of which size and type of nerve fibers?

A

Small myelinated and unmyelinated fibers

28
Q

What are “positive sx’s” associated with diabetic peripheral neuropathy?

A

Paresthesias and dyesthesias = painful sensations

29
Q

Other than peripheral neuropathy, what is another manifestation of diabetic nervous system dysfunction that is often seen?

A

Autonomic dysfunction: postural hypotension, incomplete bladder emptying (↑ infections) and sexual dysfunction

30
Q

Uremic neuropathy seen in setting of renal failure is a distal, symmetric neuropathy often associated w/ what signs and sx’s?

A

Muscle cramps + distal dysesthesias + ↓ DTRs

31
Q

Which type of neuropathy is the most common paraneoplastic form and which malignancy is it most commonly associated with?

A

Sensorimotor neuronopathy in setting of Small cell lung cancer = most common

32
Q

What is a a distinctive presentation of neuropathy associated with monoclonal gammopathies?

A

POEMS: Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy, and Skin changes

33
Q

“Saturday night palsy” is due to compression of which nerve?

A

Radial nerve in the upper arm

34
Q

Which nerve is affected in Morton neuroma and what histologic finding is seen?

A
  • Interdigital nerve at intermetatarsal sites –> foot pain; “walking on a marble”
  • Histologically = perineural fibrosis
35
Q

Demyelinating forms of Charcot-Marie-Tooth (CMT) disease are associated with what morphological features?

A
  • Demyelination and remyelination including Schwann cell hyperplasia —> Onion-bulb formation
  • Hyperplasia may be so severe that involved nerve is palpably enlarged
36
Q

What is the most common subtype of hereditary motor and sensory neuropathy (CMT) disease, what is the inheritance pattern, when and how does it present?

A
  • CMT1 = group of autosomal dominant disorders
  • Presents in 2nd decade w/ slowly progressive distal demyelinating motor and sensory neuropathy
37
Q

Which structures are injured in the CMT2 variant of CMT disease and when does it present?

A

Axonal injury; typically severe w/ early childhood onset

38
Q

Familial amyloid polyneuropathies are mainly due to germline mutations in which gene?

A

Transthyretin gene