Myopathy Flashcards
What is the principle immune target of idiopathic inflammatory myopathies?
muscle tissue
What is the difference between polymyositis and dermatomyositis?
- dermatomyositis is polymyositis with skin manifestations
* Polymyositis is anidiopathic diffuse autoimmune disease of skeletal muscle
Idiopathic inflammatory myopathies results in _______ and _______ muscle weakness with an insidious onset.
proximal and symmetric
Patients with idiopathic inflammatory myopathies are at an increased susceptibility to what?
cancer
How do you distinguish a malar rash vs. heliotrope rash?
Helioptrope involves eyelids and nasolabial folds
What serum muscle enzyme will be extremely high in idiopathic inflammatory myopathies?
creatine kinase (CK/CPK)
What autoantibodies are associated with idiopathic inflammatory myopathies?
- anti-Jo-1 antibody
In idiopathic inflammatory myopathies, elevations in _______ precede clinical exacerbations
serum enzymes
What is the best confirmatory test for idiopathic inflammatory myopathies?
muscle biopsy
What is the treatment for idiopathic inflammatory myopathies? (3 part)
- physical therapy
- corticosteroids (predinosone) 1 year taper
- immunosuppressants (methotrexate) started simultaneously
In any patient with idiopathic inflammatory myopathies they must be screened for what?
occult malignancy
What antibody is elevated in mixed connective tissue disease (MCTD)?
anti-U1 RNP (ribonucleoprotein antibodies)
This is defined as a chronic functional somatic disorder resulting in widespread MSK pain.
fibromyalgia
How is fibromyalgia diagnosed?
- Based on the 2010 ACR criteria
- widespread pain index (WPI) >7
- symptom severity scale (SSS) >5
- duration of at least 3 months
- no alternative diagnosis
For an initial presentation of fibromyalgia what is the first line medication of choice?
amitriptyline (anti-depressant)