Intravascular lymphoma associated with hemophagocytic syndrome: a rare but aggressive clinical entity

@article{Bhagwati2003IntravascularLA,
  title={Intravascular lymphoma associated with hemophagocytic syndrome: a rare but aggressive clinical entity},
  author={Niyati S. Bhagwati and Stanley J. Oiseth and Lool S. Abebe and PeterH. Wiernik},
  journal={Annals of Hematology},
  year={2003},
  volume={83},
  pages={247-250}
}
We report a 55-year-old male with a diagnosis of intravascular lymphoma and hemophagocytosis. He initially presented with hemolytic anemia and splenomegaly and was successfully treated with oral steroids. His clinical course was later complicated by fever, cytopenias, hypoalbuminemia, disseminated intravascular coagulation, gastrointestinal bleeding and acute tubular necrosis. Results of an extensive investigation for fever of unknown origin were negative. Although the patient was treated… CONTINUE READING
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