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Intramastoid solitary neurofibroma mimicking middle ear carcinoma

We report an extremely rare case of intramastoid neurofibroma. A mass with destruction of the mastoid bone of a 51-year-old woman was examined with computed tomography. Subsequent magnetic resonance imaging demonstrated an ill-defined soft tissue mass with the opacification of mastoid air cells that...

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Detalles Bibliográficos
Autores principales: Shi, Zhenshan, Zhuang, Qian, Cao, Dairong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710132/
https://www.ncbi.nlm.nih.gov/pubmed/26788355
http://dx.doi.org/10.1177/2058460115608660
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author Shi, Zhenshan
Zhuang, Qian
Cao, Dairong
author_facet Shi, Zhenshan
Zhuang, Qian
Cao, Dairong
author_sort Shi, Zhenshan
collection PubMed
description We report an extremely rare case of intramastoid neurofibroma. A mass with destruction of the mastoid bone of a 51-year-old woman was examined with computed tomography. Subsequent magnetic resonance imaging demonstrated an ill-defined soft tissue mass with the opacification of mastoid air cells that had a mass effect in the same area. The patient underwent left subtotal temporal bone resection, and histological and immunohistochemical findings confirmed the lesion to be a neurofibroma. Given that similar imaging features of neurofibroma have been reported previously elsewhere in the head/neck and extremities, we suggest that it may be possible to include this tumor in the preoperative differential diagnosis.
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spelling pubmed-47101322016-01-19 Intramastoid solitary neurofibroma mimicking middle ear carcinoma Shi, Zhenshan Zhuang, Qian Cao, Dairong Acta Radiol Open Case Report We report an extremely rare case of intramastoid neurofibroma. A mass with destruction of the mastoid bone of a 51-year-old woman was examined with computed tomography. Subsequent magnetic resonance imaging demonstrated an ill-defined soft tissue mass with the opacification of mastoid air cells that had a mass effect in the same area. The patient underwent left subtotal temporal bone resection, and histological and immunohistochemical findings confirmed the lesion to be a neurofibroma. Given that similar imaging features of neurofibroma have been reported previously elsewhere in the head/neck and extremities, we suggest that it may be possible to include this tumor in the preoperative differential diagnosis. SAGE Publications 2015-12-12 /pmc/articles/PMC4710132/ /pubmed/26788355 http://dx.doi.org/10.1177/2058460115608660 Text en © The Foundation Acta Radiologica 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Shi, Zhenshan
Zhuang, Qian
Cao, Dairong
Intramastoid solitary neurofibroma mimicking middle ear carcinoma
title Intramastoid solitary neurofibroma mimicking middle ear carcinoma
title_full Intramastoid solitary neurofibroma mimicking middle ear carcinoma
title_fullStr Intramastoid solitary neurofibroma mimicking middle ear carcinoma
title_full_unstemmed Intramastoid solitary neurofibroma mimicking middle ear carcinoma
title_short Intramastoid solitary neurofibroma mimicking middle ear carcinoma
title_sort intramastoid solitary neurofibroma mimicking middle ear carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710132/
https://www.ncbi.nlm.nih.gov/pubmed/26788355
http://dx.doi.org/10.1177/2058460115608660
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AT zhuangqian intramastoidsolitaryneurofibromamimickingmiddleearcarcinoma
AT caodairong intramastoidsolitaryneurofibromamimickingmiddleearcarcinoma