ArticleCureus2025
Old Bug, New Challenge: Invasive Group A Streptococcus and a Rare Pediatric Holospinal Epidural Abscess.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Invasive group A Streptococcus (iGAS) infections have risen in the post-COVID-19 era, with significant morbidity and mortality in children. Spinal epidural abscess (SEA) is a rare, life-threatening condition, and pediatric cases are scarcely reported. SEA caused by iGAS is even more unusual, with only sporadic case reports in the literature. Herein, a challenging case of pediatric SEA due to iGAS is described, raising awareness of this clinical entity. An otherwise healthy 18-month-old girl presented with a three-day history of gait disturbance, high temperature, and seizures. Lumbar puncture revealed pus, and cultures grew group A Streptococcus. Magnetic resonance imaging demonstrated a holospinal epidural abscess. The patient was managed conservatively with serial epidural needle drainage and prolonged intravenous antibiotics. She achieved complete clinical and radiological recovery without neurological sequelae. Pediatric SEA is rare, but early recognition and appropriate management are essential to prevent irreversible complications. Clinicians should remain vigilant for spinal complications of iGAS infections to optimize outcomes.
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