JRPMS Vol 1, No 1, September 2017, p.14-18
doi: 10.22540/JRPMS-01-014
PDF  
Review Article
Physiotherapy in Juvenile Dermatomyositis
Theodora Polychronopoulou
- Physiotherapist, Athens, Greece
Keywords: Exercise, Children, Juvenile dermatomyositis, treatment, Physiotherapy
Abstract
Juvenile dermatomyositis (JDM) is a relatively rare, multi-systemic autoimmune disease, which combines
inflammatory myopathy, characteristic cutaneous findings and symptoms of other organ systems. In JDM the basic
characteristic is the skin and muscle vasculitis, although the first sign of JDM is usually a skin rash in a V-shaped
pattern that may be red and patchy, with typically red or purplish color on the eyelids (“heliotrope” rash), cheeks,
or both. The medications used for the relief of symptoms of dermatomyositis are corticosteroids, cyclosporine,
intravenous immunoglobulin, cyclophosphamide, methotrexate, and biological agents. Evidence shows that children
with low-activity dermatomyositis should be able to safely perform aerobic exercise and resistance- based exercise
regimes to reduce disease activity and improve circulation in the resting phase, but also during exercise. Until now,
both pharmaceutical therapy and physiotherapy have been proven the best way to treat the disease so that patients
achieve complete remission without disease-related complications or any use of steroids.