Case Report: Hemophagocytic lymphohistiocytosis secondary to Escherichia coli infiltration of bone marrow in a patient with seronegative rheumatoid arthritis treated with low-dose methotrexate - Report - MDSpire

Case Report: Hemophagocytic lymphohistiocytosis secondary to Escherichia coli infiltration of bone marrow in a patient with seronegative rheumatoid arthritis treated with low-dose methotrexate

  • By

  • Ziping Liu

  • Fengjian Li

  • Yunhong Liu

  • Xueyan Chen

  • July 13, 2026

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Clinical Report: Hemophagocytic Lymphohistiocytosis Induced by E. coli

Background

Hemophagocytic lymphohistiocytosis (HLH) is a severe condition characterized by excessive immune activation and inflammation, often triggered by infections or underlying diseases. Early diagnosis is crucial, as HLH can mimic septic shock and lead to significant morbidity and mortality.

Data Highlights

No numerical data or trial data presented in the article.

Key Findings

  • HLH can occur secondary to infections, such as E. coli urinary tract infections.
  • The presence of hemophagocytic cells in bone marrow can indicate HLH, especially when accompanied by significant clinical symptoms.
  • This case involved a seronegative rheumatoid arthritis patient on low-dose methotrexate.
  • Severe pancytopenia was observed in the patient.
  • Evaluation of bone marrow smears is essential when hemophagocytes are present in the context of severe infections.

Clinical Implications

Clinicians should maintain a high index of suspicion for HLH in patients with severe infections, particularly those with underlying autoimmune conditions or on immunosuppressive therapy. Prompt diagnosis and intervention are critical to improve outcomes in these patients.

Conclusion

This case underscores the need for vigilance in diagnosing HLH in the context of severe infections, particularly in immunocompromised patients. Early recognition and management are essential to mitigate the risks associated with this life-threatening condition.

Related Resources & Content

  1. Diagnosis and investigation of suspected haemophagocytic lymphohistiocytosis in adults: 2023 Hyperinflammation and HLH Across Speciality Collaboration (HiHASC) consensus guideline - PubMed
  2. Recommendations for the management of hemophagocytic lymphohistiocytosis in adults | Blood | American Society of Hematology
  3. Clinical Rheumatology — Influence of Folate Pathway Genetic Variants on Methotrexate Treatment Outcomes in Patients with Rheumatoid Arthritis
  4. Clinical Rheumatology — Arthritis Onset in a 57-Year-Old Male Following R-CHOP Treatment for Non-Hodgkin Lymphoma
  5. Infection — Septic Arthritis Due to Ureaplasma urealyticum in an Immunocompromised Individual with Hypogammaglobulinemia Following Rituximab Treatment
  6. Clinical Rheumatology — Leprosy in Rheumatology: A Complex Condition to Recognize
  7. Diagnosis and investigation of suspected haemophagocytic lymphohistiocytosis in adults: 2023 Hyperinflammation and HLH Across Speciality Collaboration (HiHASC) consensus guideline - PubMed
  8. Recommendations for the management of hemophagocytic lymphohistiocytosis in adults | Blood | American Society of Hematology
  9. Frontiers | Case Report: Bilateral adrenal hemorrhage and hemophagocytosis in the reticuloendothelial system caused by Escherichia coli in a young woman: an autopsy case

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