A rare case of hepatosplenic gamma‐delta T‐cell lymphoma and secondary hemophagocytic lymphohistiocytosis

摘要

Key Clinical Message Hepatosplenic gamma‐delta T‐cell lymphoma with concurrent hemophogocytic lymphohistiocytosis is a rare but well‐recognized clinical scenario, associated with a grim prognosis. Clinicians must be aware of this aggressive type of lymphoma so that a prompt diagnosis can be made with timely initiation of systemic therapy and referral for bone marrow transplant.