Pregled bibliografske jedinice broj: 638897
Juvenilni dermatomiozitis
Juvenilni dermatomiozitis // Reumatizam, 59 (2) (2012), 63-72 (podatak o recenziji nije dostupan, pregledni rad, stručni)
CROSBI ID: 638897 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Juvenilni dermatomiozitis
(Juvenile dermatomyositis)
Autori
Tambić Bukovac, Lana ; Perica, Marija ; Vidovic, Mandica ; Lamot, Lovro ; Harjacek, Miroslav ;
Izvornik
Reumatizam (0374-1338) 59 (2)
(2012);
63-72
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pregledni rad, stručni
Ključne riječi
Juvenilni dermatomiozitis
(Juvenile dermatomyositis)
Sažetak
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.
Izvorni jezik
Hrvatski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-1083107-0351 - Uloga biomarkera u patofiziologiji seronegativnih spondiloartropatija (Harjaček, Miroslav, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Dječja bolnica Srebrnjak
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- SCOPUS