Examining the origin of posttransplant lymphoproliferative disorder in a patient after a second allogeneic hematopoeitic stem cell transplantation for relapsed BCR-ABL positive acute lymphoblastic leukemia

J Pediatr Hematol Oncol. 2011 Jan;33(1):50-4. doi: 10.1097/MPH.0b013e3181ed336f.

Abstract

Background: Posttransplant lymphoproliferative disease (PTLD) is a serious complication because of the reactivation of the Epstein-Barr virus (EBV). Although after solid organ transplantation (SOT) EBV is typically of recipient origin, after hematopoietic stem cell transplantation (HSCT) donor-derived B cells are usually the source of the EBV-induced lymphoproliferation.

Observation: We report a unique presentation of an EBV-associated PTLD in a 13-year-old boy who underwent 2 subsequent HSCTs from 2 different-sex donors for BCR-ABL-positive acute lymphoblastic leukemia (ALL) and relapses of leukemia, respectively. The PTLD tissue was analyzed for the origin of both B cells and T cells of the lesion. Chimerism analysis done with short tandem repeat systems (STR) showed no autologous signals; approximately 50% of the cells were from the first and second donors, respectively. XY-fluorescence in situ hybridization showed a B-cell PTLD originating from the first donor surrounded by T cells from the second donor.

Conclusion: This case shows that EBV-infected B cells from a first donor can be the source of a PTLD after a second myeloablative HSCT from a different donor.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • B-Lymphocytes / virology
  • Epstein-Barr Virus Infections / drug therapy
  • Epstein-Barr Virus Infections / etiology*
  • Epstein-Barr Virus Infections / virology
  • Fusion Proteins, bcr-abl / genetics*
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Lymphoproliferative Disorders / drug therapy
  • Lymphoproliferative Disorders / etiology*
  • Lymphoproliferative Disorders / virology
  • Male
  • Postoperative Complications / drug therapy
  • Postoperative Complications / etiology*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / therapy*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / virology
  • Recurrence
  • Tissue Donors
  • Transplantation, Homologous

Substances

  • abl-bcr fusion protein, human
  • Fusion Proteins, bcr-abl