Breast neurofibroma: A case report

INTRODUCTION: Neurofibromatosis type 1 or Von Recklinghausen disease is a rare autosomal dominant hereditary disease with total penetrance. It is characterized by an extreme clinical variability that is also found within the same family. PRESENTATION OF CASE: We report a case of neurofibroma excepti...

Descripción completa

Detalles Bibliográficos
Autores principales: Watik, F., Harrad, M., Sami, Z., Mahdaoui, Sakher, Boufettal, Houssine, Samouh, Naima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482922/
https://www.ncbi.nlm.nih.gov/pubmed/36057250
http://dx.doi.org/10.1016/j.ijscr.2022.107533

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482922/
https://www.ncbi.nlm.nih.gov/pubmed/36057250
http://dx.doi.org/10.1016/j.ijscr.2022.107533

Ejemplares similares