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Coagulation disorders in patients with severe hemophagocytic lymphohistiocytosis.

Sandrine ValadeBérangère S JolyAgnès VeyradierJehane FadlallahLara ZafraniVirginie LemialeAmélie LaunoisAlain StepanianLionel GalicierClaire FieschiAdrien MirouseJean Jacques TudesqAnne-Claire LepretreElie AzoulayMichael DarmonEric Mariotte
Published in: PloS one (2021)
Hyperfibrinolysis may be the primary mechanism responsible for hypofibrinogenemia and may also participate in ADAMTS13 degradation. Targeting the plasmin system appears as a promising approach in severe HLH-related coagulation disorders.
Keyphrases
  • early onset
  • drug induced
  • cancer therapy