Peripheral Neuropathies Flashcards

1
Q

What are the etiologies for peripheral neuropathies?

A
  • Degenerative
  • Neoplastic
  • Metabolic
  • Nutritional
  • Inflammatory
  • infectious
  • Traumatic
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2
Q

What signs are common in Neruopathic syndromes?

A
  • Neruogenic muscle atrophy
  • Flaccid paresis/paralysis
  • Reduced or absent reflexes
  • Decreased pain response
  • Proprioceptive deficits
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3
Q

Examples of Degenerative, Metabolic, Neoplastic, Infectious, and Inflammatory Peripheral Neruopaties?

A
  • Degenerative:
    • Giant axonal neuropathy
    • Hypertrophic neuropathy
    • Birman Cat distal neuropathy
  • Metabolic:
    • Diabetic neuropathy
    • Hyperchylomicronemia
    • Hypothyroidism
  • Neoplastic
    • Nerve sheath tumor
    • Leukemia
  • Infectious
    • Bostulism, Tetanus
    • Tick paralysis
    • Toxoplasma, Neospora
  • Inflammatory
    • Coonhound paralysis
    • Idiopathic Polyradiculoneuritis
    • Idiopathic, immune-mediated
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4
Q

What is the diagnostic pathway for peripheral neruopaties?

A
  • Accurate localization based on examination
  • Reference access
  • Clinical features and characteristics alone
  • Electromyography and nerve conduction velocity studies
    • Fibrillation potentials; positive sharp waves
    • Complex repetitive disharges; myotonic discharges
    • MNCV, SNCV, RNS
  • MRI
  • Nerve and muscle biopsy
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5
Q

What are the signs of Traumatic Neuropathy? how is it Dx? Tx?

A
  • Nomoparesis
  • Traction, compression, missile, bite, injection, surgical, ischeia
  • LMN signs
  • Variable return of function
    • Axon intact
    • Axon disrupted, support intact
    • Severed axon and support
  • Dx: history, clin signs, EMG, NCV
  • Tx:
    • Surgical
    • Conservative care
    • Amputate if non-functional or no improvement
      • 4-6 weeks in most
      • Rare recovery after 4 months
      • Axons regrow at 1-4mm/day
  • Very common
  • Even worse is when they are iatrogenic (injection site, compression from leg ties during surgery)
  • Cautiously pessimistic prognosis for most patients
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6
Q

What is Facial Nerve Paralysis? Dx? Tx?

A
  • Mononeuropathy
  • Etiology
    • Otitis media
    • Hypothyroidism
    • Trauma
    • Idiopathic (75% of dogs, 25% of cats)
  • Dx:
    • clinical
    • eliminate differentials
    • EMG
  • Tx: supportive
  • Poor prognosis for recovery
  • Incredibly common, often goes unrecognized, may be an “old lesion”
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7
Q

What is Trigeminal Neuritis?

A
  • Idiopathic, bilateral
  • Acute onset jaw paralysis
    • Some clients will present the dog for polydipsia
  • Concurrent neuropathy
    • CN7, Sensory CN5
    • Horner’s
  • Dx: Clinical
  • Tx: Supportive
  • Good Prognosis
  • DDx: leukemia, mononuclear cell neoplasia, rabies
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8
Q

What is Coonhound Paralysis/Idiopathic Polyradiculoneuritis?

A
  • Hunting dogs (CP) or any breed (IP)
  • Common polyneuropathy
  • Clinical presentation
    • onset 7-11 days post exposure
    • Progressive over 12 hours or up to 10 days
    • LMN signs
    • Normal from neck up
    • Persists up to 3 months
  • Severe- affect facial nerve, voice, breathing
  • Dx:
    • Clinical
    • EMG/MNCV- may be normal
    • CBC/Chem - normal
  • Tx:
    • supportive
    • Mechanical ventilation in some cases
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9
Q

What is Tick Paralysis?

A
  • A NM jjunction disorder (NOT a neuropathy)
  • 5-9 days post-attachment
  • Progressive over 1-3 days
  • Clinical signs:
    • Diffuse LMN signs
    • Voice change, cough, dysphagia
    • Normal cranial nerves
    • Respiratory paralysis
  • Tx:
    • Tick removal ⇢ rapid recovery
    • Isoxazolone preventatives to prevent
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10
Q

What is Botulism?

A
  • A NM junction disease (Type C toxin)
  • Progressive ascending LMN paralysis
  • Additional Findings
    • Megaesophagus
    • KCS
    • Dysphagia
    • Cranial nerve dysfunction
  • Uncommon
  • Tx: supportive
    • No C antitoxin
    • 14-24 days for spontaneous recovery
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11
Q

What is Botulism?

A
  • A NM junction disease (Type C toxin)
  • Progressive ascending LMN paralysis
  • Additional Findings
    • Megaesophagus
    • KCS
    • Dysphagia
    • Cranial nerve dysfunction
  • Uncommon
  • Tx: supportive
    • No C antitoxin
    • 14-24 days for spontaneous recovery
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12
Q

What is Infectious polyradiculoneuritis?

A
  • Protozoal disease
    • Neospora caninum
    • Toxoplasma gondii (?)
  • Puppies <3mo
  • Clinical Signs:
    • extensor rigidity of pelvic limbs
    • Meningoencephalomyelitis, myositis
  • Dx: Serology, Cytology, histopathylogy
  • Tx:
    • Clindamycin, TMS, pyrimethamine
    • Ponazuril, toltrazuril
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13
Q

What is Chronic Inflammatory Demyelinating Polyneuropathy / Chronic Relapsing Polyneuropathy / Idiopathic Unclassified Demyelinating Polyneuropathy?

A
  • Poorly classified and spontaneous
  • Variable onset of symptoms and peripheral nerve dysfunction
  • Paresis or paralysis involving all 4 limbs is the expected
  • Recovery is spontaneous in many
  • Immunosuppression helps with some forms
  • One of the main differentials for Idiopathic polyradiculoneuritis.
    • Biopsy is the only wat to confirm
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14
Q

What are some breed specific polyneuropathies?

A
  • Idiopathic polyneuropathy of alaskan malamutes (IPAM)
  • Boxer dog progressive anonopahty
  • Birman cat distal polyneuropathy ( and bengal cat polyneuropathy)
  • Laryngeal paralysis polyneuropathy compled of Dalmation and Rottweiler
  • Sensory neruopathy of Pointer dogs
  • Sensory neuropathy of longhaired dachshunds
  • Dancing Doberman Disease
  • Giant axonal neuropathy of German shepherd dogs
  • Golden retriever hypomyelinating polyneuropathy
  • Hypertrophic neuropathy of Tibetan
  • Rottweiler distal sensorimotor polyneuropathy
  • Neuroaxonal dystrophy of Spanish water dogs
  • Polyneuropathy in Black Russian Terrier dogs
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15
Q

What issues does Tetanus cause? How?

A
  • Tetanospasmin from C. tetani
    • Inhibits glycine and GABA release
    • Protected from anti-toxin in neuron
  • Generalized muscle stiffness, sardonic grin, laryngeal spasm
  • Infected wounds or surgery sites
  • Develop over 2-7 days
  • Takes 30-45 days to resolve
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16
Q

How is Tetanus managed

A
  • Penicillin or metronidazole (latter is preferred)
  • Muscle relaxants
    • Acepromazine and methocarbamol: commonly recommended protocol, may need to administer methocarbamol hourly and acepromazine every 4 hours
    • Phenobarbital, diazepam, midazolam, and magnesium: more effective, especially in more severe cases
    • Gabapentin - may help inhibit extensor tone
  • Nutritional support
  • Tetanus anti-toxin is not effective
17
Q

What are the different types of Sensory neuropathies?

A
  • Hereditary or idiopathic
    • longhaired dachshunds
    • English pointer
  • Sensory and/or sensorimotor
    • Border collie, Rottweiler, Golder Retriever
  • Proprioceptive loss, loss of pain perception, self-mutilation, megaesophagus
  • Rare
18
Q

What are some other movement disorders?

A
  • Tremors and Fasciculations
  • Tetany
  • Myokymia
  • Neuromyotonia
  • Cyoclonus (chorea)
19
Q

What is Shaker dog syndrome

A
20
Q

What is the difference between a Benign Postural Tremor and a benign Essential Tremor

A