Lecture 18 Flashcards

(28 cards)

1
Q

What is the other terminology for neuromuscular diseases?

A

generalized lower motor neuron diseases

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2
Q

What are the general findings in neuromuscular diseases?

A

-decreased ability to bear weight
-decreased muscle tone and mass
-possible decreased spinal reflexes

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3
Q

What are the general clinical signs of myopathies?

A

-weakness
-crouched stance
-stiff, short-strided gait
-tremors
-possible myalgia (muscle pain)
-possible abnormal muscle size
-normal postural reactions and spinal reflexes

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4
Q

Why do myopathy patients often present with hypertrophy first, followed by atrophy?

A

-hypertrophy occurs from inflammation/swelling of muscles
-atrophy occurs once disease process starts to break down the muscles

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5
Q

Why is it important to support a suspected myopathy patient’s weight when testing postural reactions and spinal reflexes?

A

a lack of appropriate postural reaction/spinal reaction due to weakness could be mistaken for neuronal disease

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6
Q

How does the rate of atrophy differ with nerve vs muscle disease?

A

-atrophy with nerve diseases is rapid
-atrophy with muscle diseases is gradual

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7
Q

What is autoimmune polymyositis?

A

diffuse immune-mediated disease directed against skeletal muscle

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8
Q

What are potential triggers for autoimmune polymyositis?

A

-often idiopathic
-systemic lupus erythematosus
-paraneoplastic syndrome (round cell tumors in boxers)
-trimethoprim-sulfa use in dobermans

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9
Q

What are the clinical signs of autoimmune polymyositis?

A

-large breed dogs
-generalized weakness that worsens with exercise
-muscle swelling/hypertrophy followed by atrophy
-megaesophagus
-possible myalgia/shifting leg lameness
-possible signs of systemic illness

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10
Q

How is autoimmune polymyositis diagnosed?

A

-elevated CK and AST
-muscle biopsy
-rule out infectious causes

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11
Q

What is the treatment for autoimmune polymyositis?

A

-immunosuppression, starting with glucocorticoids
-months of treatment with a months-long taper

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12
Q

What are the characteristics of masticatory muscle myositis?

A

-focal immune-mediated disease
-directed against muscles of mastication

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13
Q

What are the clinical signs of masticatory muscle myositis?

A

-large breed dogs
-bilateral signs
-muscle swelling (acute)
-pain on palpation (acute)
-symmetric muscle atrophy with trismus/lockjaw (chronic)

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14
Q

What is the treatment for masticatory muscle myositis?

A

immunosuppression with prednisone +/- adjunctive immunosuppressives

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15
Q

Why is it important to NOT force the mouth open in MMM patients with trismus?

A

-exacerbates restrictive fibrosis
-can break the jaw

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16
Q

What is the prognosis for masticatory muscle myositis?

A

-good if treated early and aggressively
-some atrophy may persist

17
Q

What are the most common causes of infectious myositis?

A

protozoa
-neospora
-toxoplasma

18
Q

What is the biggest differential/rule out for infectious myositis?

19
Q

What are the clinical signs of infectious myositis?

A

-often non-specific
-possible systemic signs
-CNS and PNS effects
-young or immunocompromised animals

20
Q

How is infectious myositis diagnosed?

A

-possible increased CK
-serology or PCR with serology sample or biopsy

21
Q

What is the treatment for protozoal infectious myositis?

A

clindamycin, TMS, or ponazuril

22
Q

Which metabolic diseases can cause hypokalemic myopathy?

A

-kidney disease
-hyperthyroidism

23
Q

How is hypokalemic myopathy diagnosed?

A

-serum K+ less than 3.0 mEq/L
-CK moderately elevated

24
Q

What is the treatment for hypokalemic myopathy?

A

-potassium supplementation
-address underlying disease

25
What are muscular dystrophies?
-inherited diseases that cause muscle degeneration -deficient or abnormal myofiber cytoskeletal proteins
26
What is the signalment for muscular dystrophies?
-young animals (weeks to months) -often have X-linked inheritance -golden retrievers, labs, rottweilers, cavalier king charles spaniels
27
What are the clinical signs of muscular dystrophies?
-progressive weakness and atrophy -drooling and regurg. due to megaesophagus
28
How are muscular dystrophies diagnosed?
-DNA testing -markedly elevated CK -muscle biopsy