[Inconsolable crying revealing primary erythermalgia in a 6-month-old infant]

K-C Ahogo1, V Menet2, P Modiano1

  • 1Service de dermatologie, hôpital Saint-Vincent-de-Paul, université Catholique de Lille, boulevard de Belfort, 59020 Lille, France.

Insights

Erythermalgia, a rare vascular condition, was diagnosed in a 6-month-old infant presenting with heat-induced leg redness and pain. This case highlights the condition

Area of Science:

  • Pediatric vascular disorders
  • Neurology
  • Genetics

Background:

  • Erythermalgia is a rare peripheral vascular disease triggered by heat.
  • The primary infantile form is exceptionally rare, with no prior reported cases in infants.
  • Pathophysiology involves sodium channel alterations leading to small-fiber neuropathy.

Observation:

  • A 6-month-old infant presented with recurrent crying episodes and lower limb erythema.
  • Symptoms were exacerbated by heat and absent in cooler temperatures.
  • Standard infant investigations for crying (reflux, intussusception) were negative.

Findings:

  • Diagnosis of primary infantile erythralgia was established.
  • Genetic mutations in the SCN9A gene are associated with autosomal dominant inheritance.
  • Treatment involved analgesics and cold packs, with challenges due to analgesic resistance.

Implications:

  • This case expands the known age range for primary erythralgia to infancy.
  • Early diagnosis and management are crucial, despite treatment difficulties.
  • The condition carries a potentially poor prognosis in the pediatric population.

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