2024
DOI: 10.1097/md.0000000000039011
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Hemophagocytic lymphohistiocytosis secondary to rifampin treatment: A case report

Caihong Wang,
Junke Qiu,
Xiaoqing Huang
et al.

Abstract: Rationale: Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening systemic inflammatory syndrome characterized by an overactive immune response. This hyperactivation can arise from genetic mutations, infections, malignancies, or autoimmune disorders. Medication-induced HLH is extremely rare and requires special attention. Patient concerns: A 53-year-old female diagnosed with pulmonary and urinary tract tuberculosis. She underwent quadruple… Show more

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