Recurrent febrile syndromes-what a rheumatologist needs to know

被引:32
作者
Hoffman, Hal M. [1 ]
Simon, Anna [2 ]
机构
[1] UCSD, La Jolla, CA 92093 USA
[2] Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands
关键词
FAMILIAL MEDITERRANEAN FEVER; COLD AUTOINFLAMMATORY SYNDROME; ENCODING MEVALONATE KINASE; HEREDITARY PERIODIC FEVER; HYPER-IGD SYNDROME; HYPERIMMUNOGLOBULINEMIA-D; APHTHOUS STOMATITIS; SYNDROME TRAPS; TNF RECEPTOR; INFLAMMATORY ATTACKS;
D O I
10.1038/nrrheum.2009.40
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Rheumatologists are likely to be asked to evaluate patients with recurrent febrile syndromes, so it is important that they are familiar with the clinical and diagnostic features, pathophysiology and therapeutic options for these rare autoinflammatory disorders. These syndromes are all characterized by recurrent episodes of fever and systemic inflammation; however, some syndromes have unique historical and physical features that can help with making a diagnosis. The primary associated morbidity is systemic amyloidosis, usually with renal involvement. Diagnostic testing is mostly limited to genetic testing. NSAIDs, colchicine and corticosteroids have roles in the treatment of some of these disorders, but biologic drugs that target interleukin-1 beta are emerging as consistently effective therapies.
引用
收藏
页码:249 / 256
页数:8
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