Servicios Personalizados
Revista
Articulo
Indicadores
- Citado por SciELO
Links relacionados
- Similares en SciELO
Compartir
Revista argentina de dermatología
versión On-line ISSN 1851-300X
Resumen
ESTRELLA, V; QUIROGA, R; BERGERO, A y FERNANDEZ BUSSY, R. Neurofibromatosis: Plexiform Neurofibroma Localized In Mamma. A Propos Of A Case. Rev. argent. dermatol. [online]. 2010, vol.91, n.1, pp.00-00. ISSN 1851-300X.
The Neurofibromatosis was described by von Recklinghausen in 1882. It is a dominant autosomic genodermatosis with a high penetration, variable clinic and progressive course; it is calculate, that in 50% of the cases the origin is a spontaneous mutations (novo). The incidence is 1/3000 newly born. The clinical manifestations are: the compromise of tissues derived from neuroectoderm and mesoderm. It also has ocular symptoms, visceral injuries, neurological alterations and endocrinological pathologies. Soft pars, cutaneous tissue and bones are affected. At the present time two main clinical forms are admitted: the Classic Neurofibromatosis or type I, that represents 85-90% of the cases and the Neurofibromatosis type II (Neurofibromatosis of the bilateral hearing aid) that it ´s not so frequent.
Palabras clave : Neurofibromatosis Type I; Plexiform Neurofibroma; Von Recklinghausen.