Caso clínico: síndrome de Baboon secundario a cuerpo extraño cutáneo

Autores/as

  • Tirza Saavedra U. Hospital Clínico de la Universidad de Chile. Servicio Dermatología
  • Fernando Valenzuela A. Hospital Clínico de la Universidad de Chile. Servicio Dermatología
  • Ximena Wortsman C. Clínica Servet. Departamento de Radiología
  • Laura Carreño T. Hospital Clínico Universidad de Chile. Servicio de Anatomía Patológica

Resumen

We report the clinical case of a 12 year-old healthy pediatric patient with a history of allergic contact dermatitis to nickel. He presented a papular symmetrical scarlatiniform rash after a gunshot impact partially withdrawn that began mainly in folds, which generalized to the rest of the body. We performed high-resolution ultrasonography in the impact area showing multiple small particles around a fibrous scar. The skin biopsy was consistent with systemic contact dermatitis, and immunofluorescence resulted negative. He was treated with prednisone for 5 days and anti-TNF antihistamines with good results. Nickel contact dermatitis is common in clinical practice, but systemic contact dermatitis is less frequent and even less because of a foreign body, although it has already been described. The Baboon syndrome is a maculopapular itchy rash that begins in folds and then generalizes, one of its etiologies is nickel, it should be a type IV hypersensitivity that resolves spontaneously without scars.

Palabras clave:

Dermatitis Alérgica por Contacto, Reacción a Cuerpo Extraño, Níquel/efectos adversos, Exantema/inducido químicamente, Remisión Espontánea