Autologous peripheral stem cell transplantation for aggressive hemophagocytic syndrome associated with T-cell lymphoma: Case study and review
Version of Record online: 18 DEC 2001
Copyright © 2002 Wiley-Liss,Inc.
American Journal of Hematology
Volume 69, Issue 1, pages 64–66, January 2002
How to Cite
Jassal, D. S., Kasper, K., Morales, C. and Rubinger, M. (2002), Autologous peripheral stem cell transplantation for aggressive hemophagocytic syndrome associated with T-cell lymphoma: Case study and review. Am. J. Hematol., 69: 64–66. doi: 10.1002/ajh.10009
- Issue online: 20 DEC 2001
- Version of Record online: 18 DEC 2001
- Manuscript Accepted: 16 JUL 2001
- Manuscript Received: 27 NOV 2000
- hemophagocytic syndrome;
- T-cell lymphoma;
- peripheral stem cell transplantation
Hemophagocytic syndrome (HPS) is a rare clinical presentation infrequently associated with lymphoproliferative disorders. We describe a 29-year-old male with aggressive HPS and T-cell lymphoma managed successfully with high-dose chemotherapy and autologous peripheral stem cell transplantation (APSCT), in remission at 41 months of follow-up. In reviewing the literature, this case illustrates the 2nd longest surviving individual post stem cell transplant for aggressive HPS. Am. J. Hematol. 69:64-66, 2002. © 2002 Wiley-Liss, Inc.