Treatment in Juvenile Scleroderma.
Francesco ZulianFrancesca TirelliPublished in: Current rheumatology reports (2020)
According to the recent recommendations for Pediatric Rheumatology in Europe (SHARE), systemic treatment in localized scleroderma is needed when there is a risk for disability, such as in generalized or pansclerotic morphea and progressive linear scleroderma. In juvenile systemic sclerosis, the introduction of the severity score, J4S, has standardized the assessment of the patients in the daily practice and allowed a more tailored therapeutic approach. Since, to date, no clinical trial is available in JSSc, due to its rarity, the treatment is based on adults' experience. The recent recommendations for juvenile scleroderma represent an important instrument to standardize the treatment approach, confirm the role of methotrexate, and open new windows for effective experimental treatments, such as mycophenolate mofetil and biological agents, for severe or refractory cases.
Keyphrases
- systemic sclerosis
- interstitial lung disease
- clinical trial
- end stage renal disease
- healthcare
- multiple sclerosis
- randomized controlled trial
- chronic kidney disease
- systemic lupus erythematosus
- newly diagnosed
- minimally invasive
- study protocol
- young adults
- prognostic factors
- peritoneal dialysis
- neural network
- patient reported