Pregled bibliografske jedinice broj: 403468
Retrospective study of juvenile systemic lupus erythematosus (JSLE) over the last 20 years
Retrospective study of juvenile systemic lupus erythematosus (JSLE) over the last 20 years // 2nd Congress oft he European Academy of Paediatrics : abstracts ; u: Archives of Disease in Childhood 93 (2008) (S2)
Nica, Francuska, 2011. (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 403468 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Retrospective study of juvenile systemic lupus erythematosus (JSLE) over the last 20 years
Autori
Jelušić, Marija ; Tambić Bukovac, Lana ; Batinić, Danica ; Vidović, Mandica ; Milošević, Danko ; Vrljičak, Kristina ; Nižić, Ljiljana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
2nd Congress oft he European Academy of Paediatrics : abstracts ; u: Archives of Disease in Childhood 93 (2008) (S2)
/ - , 2011
Skup
Congress oft he European Academy of Paediatrics (2 ; 2008)
Mjesto i datum
Nica, Francuska, 24.10.2008. - 28.10.2008
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
SLE; children
Sažetak
Aim was to analyze characteristics of the presenting and cumulative clinical features, immunologic manifestations, disease activity and outcome of 62 Croatian children with JSLE, followed between 1987 and 2007. There were 62 children, 52 girls and 10 boys, with the mean age at disease onset (± ; SD) 12.9± ; 2.4 years. Fifty-eight patients were followed for a mean period of 6.9± ; 5.3 yrs. The commonest presenting clinical features were constitutional (fever, fatigue) (68%), arthralgias (56%), renal involvement (53%) and malar rash (29%). Renal biopsy revealed class IV lupus nephritis (LN) in 15 (45, 5%), class III LN in 9 (27, 3%), class II LN in 5 (15, 1%) and class V LN in 4 (12, 1%) cases. The patients presented significantly altered laboratory parameters including deficiency of complement C3 (93%) and C4 (95%), high ESR (95%), cytopenia (73%) and positive anti-dsDNA (100%). Only two patients had severe opportunistic infections: CNS nocardiosis and multifocal staphylococcal osteomyelitis, both with good outcome. Due to clinical presentation and laboratory data most patients were treated with oral corticosteroids, followed by cyclophosphamide, pulse steroid, hydroxychloroquine and azathioprine. During the study period two patients died, one because catastrophic antiphospholid syndrome, other because of terminal renal failure. There is no significant difference in clinical, immunopathological features and therapy regimens in our patients compared to those in most paediatric SLE studies.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
Napomena
Rad je kao poster prezentiran i na skupu 15th European Paediatric Rheumatology Congress, održanom od 12.-15.09.2008.g., London, Velika Britanija ; Knjga sažetaka objavljena u casopisu Pediatric Rheumatology (2008) str. 380-380.
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Kristina Vrljičak
(autor)
Lana Bukovac
(autor)
Danica Batinić
(autor)
Marija Jelušić
(autor)
Danko Milošević
(autor)
Ljiljana Nižić Stančin
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE