Brucellosis-Induced Hemophagocytic Lymphohistiocytosis

  • Al Noumani J
  • Al Busaidi I
  • Al Hajri M
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Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a fatal syndrome, which can be primary or triggered by a systemic disease or an infection. The commonly reported infectious causes of secondary HLH include Epstein-Barr virus (EBV), cytomegalovirus (CMV), mycobacterium, and leishmaniasis among other infections. In this case report, we report a 50-year-old woman with brucellosis-related HLH after presenting with prolonged fever, hepatosplenomegaly, and cytopenia.

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Al Noumani, J., Al Busaidi, I., & Al Hajri, M. (2021). Brucellosis-Induced Hemophagocytic Lymphohistiocytosis. Cureus. https://doi.org/10.7759/cureus.15677

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