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Unusual muscular injury in an infant with severe H1N1 infection
Romain Guedj1, Isabelle Desguerre, Anaïs Brassier
1Service de Réanimation Polyvalente et Néonatale, Hôpital Necker-Enfants Malades, Assistance Publique des Hôpitaux de Paris, Faculté de Médecine, Université Paris-Descartes, Paris, France.
Insights
This case study documents unilateral orbital myositis in an infant with H1N1 influenza. Prompt treatment led to a favorable outcome, highlighting H1N1
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Ophthalmology
Background:
- Pandemic H1N1 influenza can cause severe, multi-organ complications.
- Orbital myositis is a rare inflammatory condition affecting eye muscles.
Observation:
- An 8-month-old boy presented with status epilepticus and hemodynamic instability.
- He exhibited unilateral orbital myositis and acute rhabdomyolysis.
- Metabolic and genetic screening was conducted due to severe myolysis.
Findings:
- The patient's condition improved following corticosteroid administration and supportive care.
- No sequelae were observed at hospital discharge.
- H1N1 infection was associated with unusual muscle injury and potential multi-organ failure.
Implications:
- This case highlights a rare association between H1N1 influenza and orbital myositis.
- Severe myolysis in this context warrants investigation for underlying metabolic or genetic disorders.
- Early recognition and management are crucial for favorable outcomes in pediatric H1N1 complications.
Abstract:
We report the first well-documented case of unilateral orbital myositis in an 8-month-old boy with life-threatening pandemic H1N1 infection. He presented with status epilepticus and hemodynamic failure associated with unusual right orbital myositis and acute rhabdomyolysis. Because of severe myolysis, metabolic screening was performed to exclude metabolic and genetic etiologies. After corticosteroid administration and symptomatic support, the disease evolution was favorable, without sequelae at hospital discharge. H1N1 influenza infection may be associated with multiple organ failure, and complicated by unusual muscle injury. The presence of intense myolysis should alert practitioners to potential metabolic and genetic etiologies.
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