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Published on: February 24, 2023
Hemophagocytic Syndrome Associated with Mycoplasma pneumoniae Pneumonia
1Department of Pediatrics, Disaster Medical Center, 3256 Midori-cho, Tachikawa, Tokyo 190-0014, Japan.
Abstract:
Mycoplasma pneumoniae (Mp) sometimes causes immunological complications in children. We present a rare case of hemophagocytic syndrome (HPS) caused by Mp in a previously healthy 7-year-old Japanese girl. A chest radiograph obtained to evaluate the source of her fever showed infiltration in the lower right lung with mild splenomegaly. We could diagnose the patient with HPS on the basis of the hemophagocytic-lymphohistiocytosis- (HLH) 2004 criteria. She met the criteria for fever, splenomegaly, neutrophil count (<1,000/ μ L), platelet count (<10.0 × 10(4)/ μ L), fasting triglyceride level (>265 mg/dL), and ferritin level (>500 ng/mL). Furthermore, a peripheral blood smear showed an increased number of monocytes/macrophages with erythrophagocytosis. Treatment with clarithromycin and prednisolone, which was initiated soon after the diagnosis, was successful. Mp infection might partly progress to HPS in certain conditions. Clinicians should be aware of HPS caused by Mp and start appropriate treatment as soon as possible if the disease is suspected.
Insights
Mycoplasma pneumoniae can cause hemophagocytic syndrome (HPS) in children. Early diagnosis and treatment with antibiotics and steroids are crucial for successful outcomes in these rare cases.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Hematology
Background:
- Mycoplasma pneumoniae (Mp) infections are common in children and can lead to immunological complications.
- Hemophagocytic syndrome (HPS), also known as hemophagocytic lymphohistiocytosis (HLH), is a rare but severe hyperinflammatory condition.
Purpose of the Study:
- To report a rare case of Mycoplasma pneumoniae-induced hemophagocytic syndrome in a child.
- To highlight the clinical presentation, diagnostic criteria, and successful management of this condition.
Main Methods:
- A case study of a 7-year-old Japanese girl diagnosed with HPS.
- Diagnosis was confirmed using the HLH-2004 criteria, including fever, splenomegaly, cytopenias, elevated triglycerides, and high ferritin levels.
- Peripheral blood smear analysis revealed erythrophagocytosis by monocytes/macrophages.
Main Results:
- The patient presented with fever, splenomegaly, neutropenia, thrombocytopenia, hypertriglyceridemia, and extremely high ferritin levels.
- Erythrophagocytosis was observed in the peripheral blood smear.
- Successful treatment was achieved with clarithromycin and prednisolone.
Conclusions:
- Mycoplasma pneumoniae infection can precipitate hemophagocytic syndrome in susceptible children.
- Clinicians should maintain a high index of suspicion for Mp-associated HPS.
- Prompt diagnosis and initiation of appropriate antimicrobial and anti-inflammatory treatment are vital for patient recovery.
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