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• W2175063706 abstract "Hemophagocytic lymphohistiocytosis (HLH) is a syndrome characterized by severe hyperinflammation due to an overwhelming ineffective immune response to different triggers. Most important symptoms are fever, hepatosplenomegaly and cytopenias. Biochemical signs include elevated ferritin, hypertriglyceridemia and low fibrinogen. Hemophagocytosis in the bone marrow is a hallmark of this syndrome. Based on the pathogenetic mechanism, it can be classified into primary (inherited) or secondary (acquired) HLH. We report, to our knowledge, the first case of acquired hemophagocytic syndrome that arose in a 20-year-old man affected by synovial sarcoma as a complication during chemotherapy." @default.
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• W2175063706 date "2015-11-01" @default.
• W2175063706 modified "2023-10-08" @default.
• W2175063706 title "Acquired hemophagocytic syndrome in a patient with synovial sarcoma: a case report" @default.
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• W2175063706 doi "https://doi.org/10.4155/fso.15.27" @default.
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