The riddle of multinucleated “floret-like” giant cells and their detection in an extensive gluteal neurofibroma: a case report

INTRODUCTION: The neurofibromatoses are inherited tumor predisposition syndromes involving two major clinical phenotypes: neurofibromatosis type 1 (von Recklinghausen's disease) is linked to chromosome 17q, and tends to occur seven times more frequently than neurofibromatosis type 2. Neurofibro...

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Detalles Bibliográficos
Autores principales: Stanger, Katrin, De Kerviler, Sora, Vajtai, Istvan, Constantinescu, Mihai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751089/
https://www.ncbi.nlm.nih.gov/pubmed/23890233
http://dx.doi.org/10.1186/1752-1947-7-189

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751089/
https://www.ncbi.nlm.nih.gov/pubmed/23890233
http://dx.doi.org/10.1186/1752-1947-7-189

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