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Author Spotlight: Advancing Research on Candida albicans Biofilm-Associated Prosthetic Joint Infections
Published on: February 2, 2024
Erysipelothrix rhusiopathiae Prosthetic Joint Infection in an Immunocompromised Patient: A Case Report
John Mahon1, Eimear Phoenix1,2, Sonia Sundanum1
1Midlands Regional Hospital Tullamore, Tullamore, Offaly, Ireland.
Case:
We report the case of an immunosuppressed 65-year-old man with prosthetic joint infection (PJI) 23 years postoperatively because of Erysipelothrix rhusiopathiae, through hematogenous seeding of cutaneous erysipeloid. Immunotherapy was discontinued, washout was performed, and antimicrobial therapy was guided by laboratory sensitivities. The patient was discharged on suppressive oral ciprofloxacin monotherapy. First-stage revision was performed at 5 months after presentation-subsequent aspiration at 1 year postoperatively demonstrated no organisms and no leucocytes. At 18-month follow-up, the patient continues to do well and has elected not to proceed with second-stage surgery.
Conclusion:
E. rhusiopathiae is a rarely seen pathogen in PJI-it should be considered with immunosuppression and relevant exposure risks. The patient achieved good clinical outcome and has experienced no sequelae to date.
Insights
This case study highlights Erysipelothrix rhusiopathiae as a rare cause of prosthetic joint infection (PJI) in immunosuppressed patients. Early intervention and targeted antibiotics led to a successful outcome, avoiding further surgery.
Area of Science:
- Infectious Diseases
- Orthopedic Surgery
- Microbiology
Background:
- Prosthetic joint infection (PJI) poses significant challenges in orthopedic surgery.
- Erysipelothrix rhusiopathiae is an uncommon pathogen implicated in PJI, particularly in immunocompromised individuals.
- Hematogenous seeding from cutaneous erysipeloid is a potential route of infection.
Observation:
- A 65-year-old immunosuppressed male presented with PJI 23 years after initial surgery.
- The infection was caused by Erysipelothrix rhusiopathiae, likely from a cutaneous erysipeloid lesion.
- Treatment involved immunotherapy cessation, surgical washout, and tailored antimicrobial therapy.
Findings:
- The patient received suppressive oral ciprofloxacin monotherapy post-discharge.
- A first-stage revision surgery was performed 5 months after presentation.
- Postoperative aspiration at 1 year showed no organisms or leukocytes, indicating successful infection control.
- At 18 months, the patient remains clinically well, opting against a second-stage revision.
Implications:
- Erysipelothrix rhusiopathiae should be considered in the differential diagnosis of PJI, especially in patients with immunosuppression and relevant exposure history.
- This case demonstrates the feasibility of managing late-onset PJI due to E. rhusiopathiae with a combination of medical and surgical interventions.
- Successful treatment achieved a good clinical outcome without sequelae, potentially avoiding extensive reconstructive surgery in select cases.
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