Progression of a hepatosplenic gamma delta T‐cell leukemia/lymphoma on hyper CVAD / MTX and ara‐C: literature review and our institutional treatment approach

Abstract

A 24‐year‐old male presented with abdominal pain, fever, and palpable splenomegaly. His differential count revealed myelocytes, metamyelocytes, and nucleated red cells. A bone marrow biopsy confirmed a diagnosis of hepatosplenic gamma delta T‐cell leukemia/lymphoma. We describe here our center's diagnostic and treatment approach for this rare leukemia.