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Case Report: Fulminant shock due to PVL-positive Staphylococcus aureus in an adolescent—superantigen-negative sepsis with toxic shock-like features

par Attou, Rachid ;Mansour, Sohaïb;Maillart, Evelyne ;Gutierrez, Leonel Barreto;Jaafari, Ayoub
Référence Frontiers in Medicine, 13, 1729510
Publication Publié, 2026

Article révisé par les pairs

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Résumé :

Background: Panton-Valentine leukocidin (PVL)-positive Staphylococcus aureus strains are associated with severe necrotising infections and may be linked to fulminant systemic inflammatory presentations. We report an exceptionally fulminant and rapidly fatal case of PVL-positive S. aureus sepsis with toxic shock-like features and early deterioration despite escalation to veno-arterial extracorporeal membrane oxygenation (VA-ECMO). Case presentation: A previously healthy 16-year-old boy presented with chest pain, dyspnoea and circulatory collapse. Initial evaluation demonstrated massive bilateral pulmonary embolism, severe biventricular systolic dysfunction, acute kidney injury and marked systemic inflammation. He received prompt haemodynamic support, systemic thrombolysis for high-risk pulmonary embolism and empirical broad-spectrum antibiotics. Echocardiography confirmed profound myocardial dysfunction and VA-ECMO was instituted as salvage support. S. aureus grew from respiratory samples and blood cultures, with susceptibility consistent with meticillin-susceptible S. aureus. Virulence gene profiling by multiplex PCR detected lukS-PV and LukF-PV, while tst, eta and etb were not detected. Antimicrobial therapy was shifted to include antitoxin agents (clindamycin and linezolid). Intravenous immunoglobulin was not administered. Despite maximal supportive care, he developed refractory multi-organ failure and died within 24 h of ICU admission. Conclusion: PVL-positive S. aureus can, albeit rarely, be associated with an extreme toxic shock-like phenotype even when classical toxin genes are not detected. This case highlights the diagnostic and management challenges posed by atypical presentations and mixed shock physiology, and underscores the need for early recognition and rapid escalation of supportive care.