Juvenile Xanthogranuloma: An Entity With a Wide Clinical Spectrum

M. J. Hernández-San Martín, P. Vargas-Mora, L. Aranibar

Producción científica: Contribución a una revistaArtículo en revista científica indexadarevisión exhaustiva

24 Citas (Scopus)

Resumen

Juvenile xanthogranulomas (JXGs) are rare, benign lesions that belong to the large group of non-Langerhans cell histiocytoses. JXG presents with 1 or more erythematous or yellowish nodules that are usually located on the head or neck. Most JXG lesions are congenital or appear during the first year of life. Extracutaneous involvement is rare, but the literature traditionally suggests investigating the possibility of ocular compromise. JXG is mainly a clinical diagnosis, but a skin biopsy may sometimes be needed for confirmation. JXGs on the skin are self-limiting and usually do not require treatment. This review describes the clinical and therapeutic aspects of JXG, emphasizing available evidence and the diagnosis of extracutaneous involvement.
Idioma originalEspañol (Colombia)
Páginas (desde-hasta)725-733
Número de páginas9
PublicaciónActas Dermo-Sifiliograficas
Volumen111
N.º9
DOI
EstadoPublicada - ene. 2020
Publicado de forma externa

Palabras clave

  • Congenital juvenile xanthogranuloma; Systemic juvenile xanthogranuloma
  • Juvenile xanthogranuloma
  • Non-Langerhans cell histiocytosis

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