Abstract
Hemophagocytic syndrome (HPS) is a rare complication of lymphoma. We report a 70-year-old woman with human adjuvant disease who developed lymphoma-associated HPS (LAHPS) and elevated serum soluble interleukin (IL)-2 receptor. Despite intensive therapy, she died of pneumonia. Necropsy revealed a prominent spleen containing atypical T cells and many erythrophagocytizing histiocytes.
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Negishi, M., Kasama, T., Hanaoka, R. et al. Peripheral T cell lymphoma-associated hemophagocytic syndrome in a patient with human adjuvant disease. Rheumatol Int 23, 143–145 (2003). https://doi.org/10.1007/s00296-002-0281-0
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DOI: https://doi.org/10.1007/s00296-002-0281-0