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West Nile virus encephalitis causing fatal CNS toxicity after hematopoietic stem cell transplantation

Bone Marrow Transplantation volume 33, pages 109–112 (2004)Cite this article

Summary:

We describe here a patient who died of progressive CNS deterioration following allogeneic stem cell transplant with West Nile virus as the sole pathogen on the cerebrospinal fluid and brain tissue analysis. A 50-year-old male with Philadelphia chromosome-positive acute lymphocytic leukemia (ALL) underwent allogeneic PBSCT from his HLA identical sister. After engraftment, the patient developed fever with progressive and ultimately fatal neurological deterioration. Imaging studies of the brain including CT and MRI scans were remarkable for mild low attenuation lesions of the white matter. CSF analysis was negative for neoplastic cells, bacteria, AFB, CMV, HSV, fungal infections and leukemic relapse. However, serological analysis of both the serum and CSF was positive for West Nile virus-specific IgM antibodies. At autopsy, West Nile virus PCR and cultures were positive in the mid-brain tissue. Electron micrographs showed evidence of viral particles. Given the recent increase in the spread of West Nile virus infections and the increased susceptibility of BMT patients to infectious complications, West Nile virus encephalitis should be considered in patients undergoing transplantation.

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Authors and Affiliations

  1. Department of Internal Medicine, Blood and Marrow Transplantation Program, Ann Arbor, MI, USA

    P Reddy, V Ratanatharathorn, C Reynolds, S Silver, L Ayash, J L M Ferrara & J P Uberti

  2. Department of Pathology, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI, USA

    R Davenport

Authors
  1. P Reddy
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  2. R Davenport
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  3. V Ratanatharathorn
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  4. C Reynolds
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  5. S Silver
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  6. L Ayash
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  7. J L M Ferrara
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  8. J P Uberti
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Correspondence to J P Uberti.

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Reddy, P., Davenport, R., Ratanatharathorn, V. et al. West Nile virus encephalitis causing fatal CNS toxicity after hematopoietic stem cell transplantation. Bone Marrow Transplant 33, 109–112 (2004). https://doi.org/10.1038/sj.bmt.1704293

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  • DOI: https://doi.org/10.1038/sj.bmt.1704293

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