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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...

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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

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