Peripheral Neuropathies Flashcards

(44 cards)

1
Q

Neuropathic Syndrome

A

Neurogenic Muscle Atrophy

Flaccid paresis / paralysis

Reduced or absent reflexes

Decreased Pain response

Proprioceptive Deficits

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2
Q

Peripheral Neuropathies

A

Motor and sensory nerves

Mono- or Polyneuropathies

Variable Etiologies

*degenerative, neoplastic, metabolic

*nutritional, inflammatory, infectios

*Traumatic

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3
Q

Classification of Peripheral Neuropathies

Degenerative

A

giant axonal neuropathy

Hypertrophic neuropathy

Birman cat distal neuropathy

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4
Q

Classification of peripheral neuropathies

metabolic

A

Diabetic Neuropathy

Hyperchylomicronemia

Hypothyroidism

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5
Q

Classification of Peripheral Neuropathies

Neoplastic

A

Nerve Sheath Tumor

Leukemia

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6
Q

Classification of peripheral neuropathies

Infection

A

Botulism, Tetanus

Tick Paralysis

Toxoplasma, Neospora

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7
Q

Classification of peripheral neuropathies

Inflammatory

A

Coonhound paralysis

Idiopathic polyradiculoneuritis

Idiopathic , immune-mediated

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8
Q

Diagnostic pathway for Peripheral Neuropathy

A

Accurate localization based on examination

Reference access

Clinical features and characteristics alone

Electromyography and Nerve Conduction Velocity studes

MRI

Nerve and Muscle Biopsy

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9
Q

Traumatic Neuropathy

A

Monoparesis

Traction, compression, missile, bite, Injection, surgical, ischemia,

LMN signs

Variable return to function: axon intact, axon disrupted, support intact, severed axon and support

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10
Q

Traumatic Neuropathy

Diagnosis

A

History,

Clinical signs

EMG
and NCV

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11
Q

Traumatic Neuropathy

Treatment

A

Surgical

Conservative care

Amputate if non-functional or no improvement

*4-6 weeks in most

*Rare recovery after 4 months

*Axons regrow at 1-4 mm/day

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12
Q

Facial Nerve Paralysis

A

Mononeuropathy

Etiology: Otiis media, Hypothyroidism, Trauma, Idiopathic

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13
Q

Facial Nerve Paralysis

Diagnosis

A

clinical

Eliminate differentials

EMG

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14
Q

Facial nerve Paralysis

Prognosis

A

poor for recovery

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15
Q

Facial Nerve Paralysis

Treatment

A

Supportive

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16
Q
A

Facial Nerve Paralysis

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17
Q

Trigeminal Neuritis

A

Idiopathic, bilateral

Acute onset jaw paralysis

Some clients will present the dog for polydipsia

Concurrent neuropathy: CN7, Sensory of 5, Horner’s

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18
Q

Trigeminal Neuritis

Diagnosis

19
Q

Trigeminal Neuritis

Therapy

20
Q

Trigeminal Neuritis

Pronosis

21
Q

Trigeminal Neuritis

Differential Diagnosis

A

Leukemia / mononuclear cell neoplasia, rabies

22
Q
A

Trigeminal Neuritis

23
Q

Coonhound Paralysis / Idiopathic Polyradiculoneuritis

A

Hunting dogs (CP), any breed (IP)

Common polyneuropathy

24
Q

Coonhound Paralysis / Idiopathic Polyradiculoneuritis

Clinical Presentation

A

onset 7-11 days post-exposure

progressive over 12 hours or up to 10 days

LMN signs

Normal form Neck up

Persists up to 3 months

Sensory Pathways still intact

25
Coonhound Paralysis / Idiopathic Polyradiculoneuritis Level of effect
Severe affect facial nerve, voice, breathing
26
Coonhound Paralysis / Idiopathic Polyradiculoneuritis Diagnosis
Clinical EMG/MNCV: both may be normal CBC/Chemistry: normal
27
Coonhound Paralysis / Idiopathic Polyradiculoneuritis Therapy
supportive care Mechanical ventilation in some cases
28
Cat with idiopathic polyradiculoneuritis
29
Tick paralysis
A N-M juction disorder 5-9 days post attachement Progressive over 1-3 days
30
Tick paralysis Clinical Signs
Diffuse LMN signs Voice change, cough, dysphagia Normal cranial nerves Respiratory paralysis
31
Tick Paralysis Therapy
Tick removal - rapid recovery
32
Tick Pralysis Prevention
Isoxazolone preventives are most effective at preventing disease
33
Botulism
A N-M junction disease (**Type C Toxin Only**) Progressive ascending LMN paralysis Additional Findings: \*Megaesophagus \*KCS \*Dysphagia \*cranial nerve dysfunction Uncommon in dogs and cats
34
Botulism Treatment
mostly supportive No C Antitoxin 14-24 days for spontaneous recovery
35
Infectious Polyradiculoneurits
Protozoal Disease Neospora Caninum Toxoplasma Gondii Puppies \< 3 months
36
Infectious Polyradiculoneuritis Clinical Sings
Extensor Rigidity of pelvic limbs Meningoencephalomyelitis, myositis
37
Infectious Polyradiculoneuritis Diagnosis
Serology cytology Histopathology
38
Infectious Polyrradiculoneuritis Treatment
Clindamycin, TMS, Primethamine Ponazuril, Toltrazuril
39
Chronic Inflammatory Demyelinating Polyneuropathy Chronic Relapsing Polyneuropathy Idiopathic Unclassified Demyelinating Polyneuropathy
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
40
Tetanus
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
41
Tetanus Managment
Penicillin or metronidazole (latter preferred) Musle relaxant: \*Acepromazine and methocarbamol: commonly recommend protocol, may need to administer methocarbamol hourly and ace every 4 hrs \*Phenobarbital, diazepam, midazolam, magnesium: more effective, especially in more severe cases \*Gabapentin: May help inhibit extensor tone Nutritional support Tetanus anti-toxin is not effective
42
Sensory Neuropathies Hereditary or idiopathic
longhairded dachshunds English Pointer
43
Sensory Neuropathies Sensory and or sensorimotor
Border collie, Rottweiler, Golden Retriever
44
Sensory Neuropathies
Proprioceptive loss, loss of pain perception, self-mutilation, megaesophagus