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

Clinical Case Reports

Abhijit Saste¹  Javier Arias-Stella² 

[1] Department of Hematology and Oncology, Henry Ford Hospital, Detroit, Michigan;Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, Michigan

关键词: Chemotherapy;    hematology;    leukemia;    lymphoma;    medical oncology;   

DOI  :  10.1002/ccr3.453

来源: Wiley

【 摘 要 】

Key Clinical Message

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.

【 授权许可】

CC BY-NC   
© 2015 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

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