Juvenilni dermatomiozitis (CROSBI ID 194759)
Prilog u časopisu | pregledni rad (stručni)
Podaci o odgovornosti
Tambić Bukovac, Lana ; Perica, Marija ; Vidovic, Mandica ; Lamot, Lovro ; Harjacek, Miroslav ;
hrvatski
Juvenilni dermatomiozitis
Juvenile dermatomyositis is the most common idiopathic inflammatory myopathy in children, and presents a heterogeneous group of subacute, chronic and acute diseases of skeletal muscles. Its unique presentation is marked with characteristic skin rushes and progressive muscle weakness. JDM is clinically distinct from adult dermatomyositis, because it is a systemic vasculopathy not associated with malignancy and it often overlaps with other chronic childhood inflammatory diseases. Although immunopathology of JDM is complex, new studies are completing our knowledge of disease pathogenesis. Corticosteroids represent the first line therapy, afterwards combined with immunomodulatory drugs and biological agents. Better knowledge of the disease combined with modem treatment modalities resulted in reduced mortality rates and in much improved quality of life in patients with JDM.
Juvenilni dermatomiozitis
nije evidentirano
engleski
Juvenile dermatomyositis
nije evidentirano
Juvenile dermatomyositis
nije evidentirano