SciELO - Scientific Electronic Library Online

 
vol.91 número1Lesiones dermatológicas del síndrome de Apert: A propósito de un caso clínico índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

  • No hay articulos citadosCitado por SciELO

Links relacionados

  • No hay articulos similaresSimilares 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.

        · resumen en Español     · texto en Español     · Español ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons