Epidemiology
Etiology and pathophysiology
Middle aged females
Idiopathic/associated with connective tissue disorders/malignancy
Type 4 hypersensitivity against muscle fibres
Presentation of polymyositis and dermatomyositis
Skin features specific to dermatomyositis
Symmetrical proximal muscle weakness +- tenderness
Raynaud’s
Resp muscle weakness, ILD
Dysphagia, dysphonia
Skin features specific to dermatomyositis
Investigations
High CK, LDH, AST, ALT, aldolase
Anti synthetase, Jo1 AB
EMG
Muscle biopsy
ANA
Management
Prednisolone