Polymyositis Flashcards
What is polymyositis?
An idiopathic inflammatory myopathy that causes symmetrical, proximal muscle weakness.
Pathogenesis of polymyositis
T-cell medicated cytotoxic process directed against unidentified muscle antigens. CD8 T cells, along with macrophages, surround healthy nonnecrotic muscle fibres and eventually invade and destroy them.
Presentation of polymyositis
Symmetrical, proximal muscle weakness in upper and lower extremities
Insidious onset
Difficulty with particular activities
Some patients have myalgia
Dysphagia in 1/3 of patients (poor prognostic sign)
ILD in 5-30% of patients
Polymyositis investigations
Raised inflammatory markers
Raised CK (more than 10 times the normal level)
ANA, anti-Jo-1 and Anti-SRP positive
MRI to localise extent of muscle involvement
Electromyographic (EMG) findings in 90% of patients.
Muscle biopsy = diagnostic
Management of polymyositis
Prednisolone 40mg
Immunosuppressive drugs i.e. methotrexate or azathioprine