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Fludarabine and Rituximab in Relapsed or Refractory Hairy Cell Leukmia Variant: A Case Report and Review of Literature

  • Lee, Ji Won (Departments of Internal medicine, Laboratory medicine, Veterans Health Service Medical Center) ;
  • Choi, Youn Mi (Departments of Laboratory medicine, Veterans Health Service Medical Center) ;
  • Yang, Jae Yun (Departments of Internal medicine, Laboratory medicine, Veterans Health Service Medical Center) ;
  • Han, Seung Moon (Departments of Internal medicine, Laboratory medicine, Veterans Health Service Medical Center) ;
  • Kim, Bong Seog (Departments of Internal medicine, Laboratory medicine, Veterans Health Service Medical Center) ;
  • Nam, Seung-Hyun (Departments of Internal medicine, Laboratory medicine, Veterans Health Service Medical Center)
  • Received : 2016.08.10
  • Accepted : 2016.09.21
  • Published : 2018.12.31

Abstract

Hairy cell leukemia (HCL) is a rare chronic B cell leukemia morphologically characterized by cells with an abundant cytoplasm and hair-like projections that can be found in the peripheral blood and bone marrow. The treatment for HCL is splenectomy or chemotherapy with the purine analogs pentostatin and cladribine. However, patients continue to relapse. Retreatment with the same or alternate purine analogs produces lower response rates and a shorter duration of response. Fludarabine is another purine analog widely used in treating indolent lymphoid cancers, often in combination with rituximab. Here, we report a case of HCL variant in a 60-year-old man who experienced multiple relapses after splenectomy and retreatment with cladribine. The patient was then treated with fludarabine and rituximab combination chemotherapy. After the treatment, he achieved complete remission that continued for 35 months.

Keywords

References

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