Pregled bibliografske jedinice broj: 812418
Anti-sintetaza sindrom
Anti-sintetaza sindrom // Reumatizam, 2 (2012), 53-57 (podatak o recenziji nije dostupan, pregledni rad, stručni)
CROSBI ID: 812418 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Anti-sintetaza sindrom
(Anti-synthetase syndrome)
Autori
Novak Srđan
Izvornik
Reumatizam (0374-1338) 2
(2012);
53-57
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pregledni rad, stručni
Ključne riječi
anti-sintetaza sindrom; dermatomiozitis; intersticijska bolest pluća; polimiozitis; liječenje
(antisynthetase syndrome; dermatomyositis; intersticial lung disease; polymyositis; treatment)
Sažetak
Antysynthetase syndrome is considered as a group of idiopathic inflammatory myositis with charcteristic serologic hallmark - antibodies which recognise the aminoacyl-tRNA synthetasses (ARS). Clinical picture of those patients contains myositis and/or intersticial lung disease (ILD) and/or arthritis and/or fever and/or Raynaud phenomenon and sometimes characteristic look of mechanic´s hands. Myositis can be overt, sometimes even absent, while IBP is major cause of morbidity and determines the outcome of the disease. Untill now eight different any-synthetase autoantibodies are recognised, and most frequent are findings of anti-histidyl-tRNa synthetase antibodies. Patients with other ARS autoantibodies usually have severe ILD. Drug of choice are steroids in dosage of 1 mg/kg with immunosupresive agent (azatioprin or methotrexate) while in severe IBP cyclophosphamide is needed. Recently succsesful treatment with rituximab in combination with cyclophosphamide is reported.
Izvorni jezik
Hrvatski
Znanstvena područja
Kliničke medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus
- MEDLINE