Adult onset Still's disease with persistent skin lesions complicated by secondary hemophagocytic lymphohistiocytosis.

Abstract

Dear Editor, Here we describe an interesting case of a middle-aged male patient presenting with adult onset Still’s disease (AOSD) complicated by secondary hemophagocytic lymphohistiocytosis (HLH) and generalized dermal and mucosal hyper-pigmentation. AOSD is a rare, inflammatory disease of unknown etiology, affecting primarily young adults, and… (More)
DOI: 10.1111/1756-185X.12170

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