Abstract
The adult-onset Still’s disease is an autoinflammatory polygenic rare systemic condition, nonetheless, clinically well described. Because of its sporadic presentation in adults with a potential severe inflammatory start, linked to a broad spectrum of manifestations and complications, it presents as a non-solved challenge to clinicians, with limited therapeutic options. In this article a patient´s case of the San Juan de Dios Hospital will be reviewed. Afterwards, general aspects such as clinical presentation, diagnostic criteria, associated complications y and therapeutic options will be described.
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