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CASE REPORT
Treatment of immune thrombocytopenic purpura associated with cytomegalovirus infection in a child with pre-B cell acute lymphoblastic leukaemia after central nervous system relapse
  1. Ashley R Martinez1,
  2. Megan Rose Paul2,
  3. Dennis John Kuo2
  1. 1Department of Pediatrics, University of California, San Diego, California, USA
  2. 2Department of Pediatric Hematology-Oncology, University of California, San Diego, California, USA
  1. Correspondence to Dr Dennis John Kuo, dekuo{at}ucsd.edu

Summary

A 13-year-old male patient with a history of pre-B cell acute lymphoblastic leukaemia (ALL) with isolated central nervous system relapse on maintenance chemotherapy presented with severe thrombocytopenia refractory to platelet transfusions. The patient showed only modest responses to two courses of intravenous immunoglobulin and steroids. He was found to be positive for cytomegalovirus (CMV) with modest viral load. His thrombocytopenia normalised with rituximab therapy and CMV treatment supporting the diagnosis of CMV-associated immune thrombocytopenic purpura (ITP). Following treatment, the patient continued to have a stable platelet count well above the threshold for transfusions. He continued to be intermittently treated for CMV when viral loads became detectable. This report discusses the unique management considerations of ITP in a patient undergoing therapy for ALL with a review of previously reported cases and discusses the possibility of CMV viraemia as a modulating factor.

  • paediatric oncology
  • haematology (including blood transfusion)

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Footnotes

  • Contributors All the authors (ARM, MRP and DJK) contributed to the care of the patient, and the conception, writing and editing of the manuscript.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.