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Adult-Onset Still's Disease Complicated by Secondary Hemophagocytic Lymphohistiocytosis: A Case Report
Vasileios Patriarcheas1, Vasiliki Gougoula1, Michail Makris1
1First Propaedeutic Department of Internal Medicine Aristotle University of Thessaloniki, AHEPA University Hospital Thessaloniki Greece.
Abstract:
Adult-onset Still's disease (AOSD) is a rare autoinflammatory disorder characterized by fever, rash, joint pain, and elevated ferritin levels. Systemic inflammation can trigger an exaggerated immune response, leading to secondary hemophagocytic lymphohistiocytosis (HLH). This case discusses AOSD complicated by HLH in a 29-year-old female, emphasizing prompt recognition and management.
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