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Adult-onset Still’s disease with hemophagocytic lymphohistiocytosis and minimal change disease

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome characterized by diverse etiologies and a high risk of misdiagnosis. Autoinflammatory disorders, such as adult-onset Still’s disease (AOSD), are often underrecognized as contributing factors. Minimal change dis...

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Autors principals: Guo Dong-hua, Wei Li, Jia Jun-ya
Format: Artigo
Idioma:Inglês
Publicat: De Gruyter 2026-01-01
Col·lecció:Open Life Sciences
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Accés en línia:https://doi.org/10.1515/biol-2025-1228
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