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Hematology ReportsHematology Reports
  • Case Report
  • Open Access

29 January 2014

3 Pages

Reduced Intensity Allogeneic Stem Cell Transplant for Treatment of Blastic Plasmacytoid Dendritic Cell Neoplasm

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1
Hematology Department, University Hospital Walsgrave, Coventry CV2 2DX, UK
2
Department of Hematology, Birmingham Heartlands Hospital, Bordesley Green East, Birmingham B9 5SS, UK
3
Hematology Department, University Hopital North Staffordshire, Stoke-on-Trent ST4 7LN, UK
4
Histopathology Department, Heart of England NHS Trust, Birmingham B9 5ST, UK

Abstract

Blastic plasmacytoid dendritic cell neoplasm is a rare, aggressive tumor characterized by skin and/or marrow infiltration by CD4+ CD56+ cells. Historically, the tumor was variably thought to arise from either monocytes, T cells or NK cells giving rise to terms such as CD4+/CD56+ acute monoblastic leukemia, primary cutaneous CD4+/CD56+ hematodermic tumor and blastic NK-cell lymphoma. Whilst considerable progress has been made in understanding the histogenesis, the best modality of treatment remains to be defined. We are therefore reporting this case which was successfully treated with a T-deplete allogeneic transplant and the patient is currently alive and in remission 4 years post transplant.

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