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Hybrid Neurofibroma-Schwannoma
Neurofibromas and schwannomas are common lesions that may be idiopathic or may occur in association with neural crest genetic syndromes such as neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. A hybrid tumor that contains pathological characteristics of both neurofibroma and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852185/ https://www.ncbi.nlm.nih.gov/pubmed/27158577 http://dx.doi.org/10.7759/cureus.548 |
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author | Hussain, Namath S Specht, Charles S Frauenhoffer, Elizabeth Glantz, Michael Harbaugh, Kimberly |
author_facet | Hussain, Namath S Specht, Charles S Frauenhoffer, Elizabeth Glantz, Michael Harbaugh, Kimberly |
author_sort | Hussain, Namath S |
collection | PubMed |
description | Neurofibromas and schwannomas are common lesions that may be idiopathic or may occur in association with neural crest genetic syndromes such as neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. A hybrid tumor that contains pathological characteristics of both neurofibroma and schwannoma has been described as a rare entity. We present the clinical, radiographic, and pathological findings of such a case. |
format | Online Article Text |
id | pubmed-4852185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-48521852016-05-06 Hybrid Neurofibroma-Schwannoma Hussain, Namath S Specht, Charles S Frauenhoffer, Elizabeth Glantz, Michael Harbaugh, Kimberly Cureus Pathology Neurofibromas and schwannomas are common lesions that may be idiopathic or may occur in association with neural crest genetic syndromes such as neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. A hybrid tumor that contains pathological characteristics of both neurofibroma and schwannoma has been described as a rare entity. We present the clinical, radiographic, and pathological findings of such a case. Cureus 2016-03-30 /pmc/articles/PMC4852185/ /pubmed/27158577 http://dx.doi.org/10.7759/cureus.548 Text en Copyright © 2016, Hussain et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Pathology Hussain, Namath S Specht, Charles S Frauenhoffer, Elizabeth Glantz, Michael Harbaugh, Kimberly Hybrid Neurofibroma-Schwannoma |
title | Hybrid Neurofibroma-Schwannoma |
title_full | Hybrid Neurofibroma-Schwannoma |
title_fullStr | Hybrid Neurofibroma-Schwannoma |
title_full_unstemmed | Hybrid Neurofibroma-Schwannoma |
title_short | Hybrid Neurofibroma-Schwannoma |
title_sort | hybrid neurofibroma-schwannoma |
topic | Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852185/ https://www.ncbi.nlm.nih.gov/pubmed/27158577 http://dx.doi.org/10.7759/cureus.548 |
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