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Autoimmune Polymyositis
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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An immune-mediated primary myositis involving muscle cell degeneration, necrosis, and apoptosis. It is thought to be mediated by cytotoxic lymphocyte mechanisms.
Age of Onset: Any age of animal can be affected, however Fox Terriers are more commonly affected bewteen 2 and 4 years of age,
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Variable
Clinical Signs:
Posture and Appearance  
Exophthalmos

Movement
Generalized weakness
“Stiff” gait (shorter interstep distance and limbs in a more extended posture)

Cranial Nerves
Dysphagia
Dysphonia
Inability to open jaw

Special Functions
(e.g. respiration; urination)  

Megaesophagus

Muscle Atrophy  
Diffuse or focal muscle atrophy
Masticatory muscle atrophy

Pain Sensation  
May have muscle pain on palpation

Other

Fever​
Diffuse muscle
Unknown
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References
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