| Literature DB >> 26461152 |
Angelo Ravelli1, Sergio Davì2, Francesca Minoia2, Alberto Martini3, Randy Q Cron4.
Abstract
Macrophage activation syndrome (MAS) is a potentially life-threatening complication of rheumatic disorders that occurs most commonly in systemic juvenile idiopathic arthritis. In recent years, there have been several advances in the understanding of the pathophysiology of MAS. Furthermore, new classification criteria have been developed. Although the place of cytokine blockers in the management of MAS is still unclear, interleukin-1 inhibitors represent a promising adjunctive therapy, particularly in refractory cases.Entities:
Keywords: Hemophagocytic lymphohistiocytosis; Hemophagocytic syndrome; Interleukin-1 inhibitors; Macrophage activation syndrome; Proinflammatory cytokines; Systemic juvenile idiopathic arthritis
Mesh:
Year: 2015 PMID: 26461152 DOI: 10.1016/j.hoc.2015.06.010
Source DB: PubMed Journal: Hematol Oncol Clin North Am ISSN: 0889-8588 Impact factor: 3.722