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How I treat patients with adult onset Still's disease in clinical practice. | LitMetric

How I treat patients with adult onset Still's disease in clinical practice.

Autoimmun Rev

Department of Clinical and Biological Sciences, Center of Research of Immunopathology and Rare Diseases, Coordinating Center of the Network for Rare Diseases of Piedmont and Aosta Valley, S. Giovanni Bosco Hospital and University of Turin, Turin, Italy. Electronic address:

Published: October 2017

Adult onset Still's disease (AOSD) is a rare systemic inflammatory disease of unknown etiology characterized by four cardinal signs which are almost always present in patients: high spiking fever, arthralgia (with or without synovitis), maculo-papular salmon-pink evanescent skin rash, striking leukocytosis with neutrophilia. Here, we review the clinical features of AOSD and describe the best practice approaches for its management, reviewing available guidelines and recommendations and providing experts' insights.

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Source
http://dx.doi.org/10.1016/j.autrev.2017.07.017DOI Listing

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