Hemophagocytic syndrome in adult-onset Still’s disease (AOSD): A must for biologics?—Case report and brief review of the literature

被引:0
作者
Urs Bürgi
Adriana Mendez
Paul Hasler
Hans Dieter Hüllstrung
机构
[1] Kantonsspital Aarau,Department of Medicine
[2] Kantonsspital Aarau,Department of Laboratory Medicine
[3] Kantonsspital Aarau,Department of Rheumatology
[4] Bethesda-Spital Basel,Department of Rheumatology
来源
Rheumatology International | 2012年 / 32卷
关键词
Adult-onset Still’s disease; Biological products; Hemophagocytic lymphohistiocytosis; Reactive hemophagocytic syndrome;
D O I
暂无
中图分类号
学科分类号
摘要
A case of adult-onset Still’s disease complicated by hemophagocytic lymphohistiocytosis is reported. Its management is being discussed on the background of the latest literature with special regard on the use of high-dose corticosteroids and immunosuppressive agents.
引用
收藏
页码:3269 / 3272
页数:3
相关论文
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