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Adult onset hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome, which can develop as a complication of many disorders. Early diagnosis is essential in order to avoid a fatal outcome. To… Click to show full abstract
Adult onset hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome, which can develop as a complication of many disorders. Early diagnosis is essential in order to avoid a fatal outcome. To confirm the diagnosis of acquired HLH made in a single institution series of adult patients with HLH‐04 criteria, we applied the HScore and evaluated prognostic factors associated with clinical outcome.
Keywords:
onset hemophagocytic;
adult onset;
institution series;
hemophagocytic lymphohistiocytosis;
single institution
Journal Title: Hematological Oncology
Year Published: 2017
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Journal Title: Hematological Oncology
Year Published: 2017
Link to full text (if available)
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recommendations!