Skoči na glavni sadržaj

Liječnički vjesnik, Vol. 144 No. Supp 2, 2022.

Sažetak sa skupa

https://doi.org/10.26800/LV-144-supl2-CR77

Juvenile dermatomyositis with vasculopathy

Mia Kovačević ; School of Medicine University of Zagreb
Magdalena Kujundžić ; School of Medicine University of Zagreb
Marijana Frković ; Division for Pediatric Rheumatology, Department of Pediatrics; University Hospital Centre ZagrebSchool of Medicine University of Zagreb

Puni tekst: engleski pdf 671 Kb

str. 83-83

preuzimanja: 91

citiraj

Sažetak

Juvenile dermatomyositis (JDM) is rare, but serious disease with many possible complications. Hallmarks of this disease are heliotrope erythema, periorbital edema and Gottrone papules combined with symmetric proximal muscle weakness that usually slowly progresses over period of weeks and months. In most cases the age of onset is between 4 and 10 years. There are four subtypes of the disease with variable course, organ involvement
and long-term clinical outcome.

Ključne riječi

Infliximab, juvenile dermatomyositis, vascu- lopathy

Hrčak ID:

279893

URI

https://hrcak.srce.hr/279893

Datum izdavanja:

27.4.2022.

Posjeta: 265 *