Post-Streptococcal Myositis: Etiology of Myalgia and Severe Inflammation in a Child

Lindy J Pence1, Minal A Aundhia1, Jamal Alanni1

  • 1Cincinnati Children's Hospital, Cincinnati, Ohio.

Pediatrics
|November 17, 2025
PubMed

Insights

Post-streptococcal myositis is a rare complication of Streptococcus pyogenes infection in children. Prompt diagnosis and treatment with steroids led to full recovery in an 8-year-old girl with severe inflammation and pain.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Rheumatology

Background:

  • Streptococcus pyogenes (Group A Streptococcus) causes common pediatric infections.
  • While typically treatable, GAS infections can lead to rare but severe complications.
  • Pediatricians must maintain vigilance for these potential sequelae.

Purpose of the Study:

  • To report a rare case of post-streptococcal myositis in a pediatric patient.
  • To describe the clinical presentation, diagnostic work-up, and management of this complication.
  • To highlight the importance of considering post-streptococcal myositis in children with severe unexplained inflammation and myalgia.

Main Methods:

  • Case report of an 8-year-old female with GAS infection.
  • Clinical evaluation including physical examination, laboratory tests (creatine kinase, inflammatory markers, ASO, anti-DNase B), imaging (ultrasound/MRI), and muscle biopsy.
  • Review of existing literature on post-streptococcal myositis.

Main Results:

  • The patient presented with severe extremity pain, difficulty walking, high fevers, and thrombophlebitis.
  • Initial work-up showed non-specific inflammation and normal creatine kinase; imaging revealed myositis and fasciitis.
  • Diagnosis of post-streptococcal myositis was confirmed by elevated ASO/anti-DNase B titers; symptoms resolved rapidly with systemic steroids.

Conclusions:

  • Post-streptococcal myositis is a rare but significant complication of GAS infection.
  • This case highlights a unique presentation with thrombotic complications and extensive inflammation.
  • Pediatric muscle biopsy findings were notable for normal architecture without vasculitis or necrosis.
  • Early recognition and appropriate treatment, including systemic steroids, are crucial for favorable outcomes.

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