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Yersinia pseudotuberculosis-Associated Myositis
Koji Yokoyama1, Mitsukazu Mamada1
1Department of Pediatrics, Japanese Red Cross Wakayama Medical Center, Wakayama, JPN.
Abstract:
Yersinia pseudotuberculosis (Y. pstb.) is a Gram-negative pathogen associated with gastrointestinal infections, such as enterocolitis. While complications like reactive arthritis can occur, progression to myositis is extremely rare. This report describes a five-year-old boy who developed myositis following a Y. pstb. infection. The patient presented with a five-day history of abdominal pain, fever, and leg pain that progressed to muscle weakness, which affected his ability to walk. Laboratory results showed elevated inflammatory markers, and stool cultures confirmed Y. pstb. infection. Magnetic resonance imaging (MRI) examination revealed muscle inflammation consistent with myositis. The patient improved rapidly with conservative treatment (rest and acetaminophen) and did not require antibiotics. Thirteen years later, he remained asymptomatic. This case highlights the rare complication of myositis following Y. pstb. infection. Potential mechanisms include postinfectious immune-mediated myositis. Clinicians should be aware of this possibility, and conservative treatment may suffice for recovery.
Insights
A rare case of myositis developed in a child after Yersinia pseudotuberculosis infection. This post-infectious complication resolved with conservative care, highlighting awareness for clinicians.
Area of Science:
- Microbiology
- Infectious Diseases
- Pediatrics
Background:
- Yersinia pseudotuberculosis (Y. pstb.) is a Gram-negative bacterium causing gastrointestinal infections like enterocolitis.
- While reactive arthritis is a known complication, myositis is an exceptionally rare sequela.
Observation:
- A five-year-old boy presented with fever, abdominal pain, and leg pain progressing to severe muscle weakness and inability to walk.
- Laboratory tests revealed elevated inflammatory markers, and stool cultures confirmed Y. pseudotuberculosis infection.
- MRI demonstrated muscle inflammation indicative of myositis.
Findings:
- The patient experienced rapid improvement with conservative management, including rest and acetaminophen, without antibiotic intervention.
- He remained asymptomatic 13 years post-infection, suggesting a favorable long-term prognosis.
- This case documents the extremely rare occurrence of myositis following Y. pseudotuberculosis infection.
Implications:
- The findings suggest a potential post-infectious, immune-mediated mechanism for myositis development after Y. pseudotuberculosis.
- Clinicians should consider myositis in the differential diagnosis for children with muscle weakness following Y. pseudotuberculosis infection.
- Conservative treatment approaches may be sufficient for managing this rare complication.
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