Profound autoimmune hemolysis and Evans syndrome in two asplenic patients with babesiosis

Joseph J. Shatzel, Kelsey Donohoe, Ngoc Quynh Chu, George Garratty, Kabir Mody, Elizabeth M. Bengtson, Nancy M. Dunbar

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

Background Evans syndrome (ES) is characterized by the simultaneous or sequential presence of multiple autoimmune cytopenias. It is often secondary to rheumatologic disorders or lymphoid malignancies, but has not previously been associated with babesiosis. Here we present two cases of severe cytopenias in asplenic patients precipitated by active babesiosis. Case Report The first patient had a history of Hodgkin's lymphoma in remission and autoimmune hemolytic anemia (AIHA) treated by splenectomy 12 years prior who presented with severe AIHA and thrombocytopenia after Babesia infection. The second patient had a history of ES requiring splenectomy, which relapsed after Babesia infection. Results The complex presentation and medical histories of both patients made the diagnosis challenging. Both patients' cytopenias responded to therapy, although the use of immunosuppressive agents in patients with active hematologic infections was challenging and required a multidisciplinary approach. Conclusion These two cases illustrate the possibility of babesiosis to not only reactivate ES in asplenic patients, but also precipitate increased levels of immune deregulation, potentially provoking ES, a phenomenon not previously reported.

Original languageEnglish (US)
Pages (from-to)661-665
Number of pages5
JournalTransfusion
Volume55
Issue number3
DOIs
StatePublished - Mar 1 2015

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Hematology

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    Shatzel, J. J., Donohoe, K., Chu, N. Q., Garratty, G., Mody, K., Bengtson, E. M., & Dunbar, N. M. (2015). Profound autoimmune hemolysis and Evans syndrome in two asplenic patients with babesiosis. Transfusion, 55(3), 661-665. https://doi.org/10.1111/trf.12901