NK/T-cell bone lymphoma-induced hemophagocytic lymphohistiocytosis: A clinical case report
- PMID: 40247956
- PMCID: PMC12005217
- DOI: 10.1016/j.radcr.2025.03.025
NK/T-cell bone lymphoma-induced hemophagocytic lymphohistiocytosis: A clinical case report
Abstract
Hemophagocytic lymphohistiocytosis (HLH) is a severe condition characterized by the secretion of large amounts of inflammatory cytokines. Lymphoma is a major cause of secondary HLH. This report describes the case of a child initially diagnosed with HLH who experienced recurrent episodes after treatment. Ten months after the initial diagnosis, a mass was discovered in the right upper limb, and pathology findings confirmed NK/T-cell lymphoma. Based on the patient's medical history, this lymphoma was considered the underlying cause of HLH. Patients diagnosed with lymphoma complicated by HLH have a worse prognosis and shorter survival compared with those without HLH. Early diagnosis and timely symptomatic treatment can significantly improve patient prognosis.
Keywords: Bone lymphoma; Case report; Hemophagocytic lymphohistiocytosis; NK/T-cell lymphoma.
© 2025 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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