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Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence

Coexisting vestibular schwannoma (VS) with fibrous dysplasia is extremely rare. Here, we represent the case of a 48-year-old female with coexisting VS and fibrous dysplasia of overlying occipital bone. After proper evaluation, the patient underwent surgery and microscopic total excision of the right...

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Autores principales: Sharma, Vikas, Kedia, Rishabh, Mohapatra, Ishani, Banerjee, Anirban Deep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896621/
https://www.ncbi.nlm.nih.gov/pubmed/31903382
http://dx.doi.org/10.4103/ajns.AJNS_73_19
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author Sharma, Vikas
Kedia, Rishabh
Mohapatra, Ishani
Banerjee, Anirban Deep
author_facet Sharma, Vikas
Kedia, Rishabh
Mohapatra, Ishani
Banerjee, Anirban Deep
author_sort Sharma, Vikas
collection PubMed
description Coexisting vestibular schwannoma (VS) with fibrous dysplasia is extremely rare. Here, we represent the case of a 48-year-old female with coexisting VS and fibrous dysplasia of overlying occipital bone. After proper evaluation, the patient underwent surgery and microscopic total excision of the right cerebellopontine angle lesion was achieved. However, during surgery, bone work was extremely tedious and exposure to reach up to lesion was difficult. To the best of our knowledge, this is the first reported case of coexisting fibrous dysplasia of overlying bone and VS as histopathological diagnosis.
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spelling pubmed-68966212020-01-03 Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence Sharma, Vikas Kedia, Rishabh Mohapatra, Ishani Banerjee, Anirban Deep Asian J Neurosurg Case Report Coexisting vestibular schwannoma (VS) with fibrous dysplasia is extremely rare. Here, we represent the case of a 48-year-old female with coexisting VS and fibrous dysplasia of overlying occipital bone. After proper evaluation, the patient underwent surgery and microscopic total excision of the right cerebellopontine angle lesion was achieved. However, during surgery, bone work was extremely tedious and exposure to reach up to lesion was difficult. To the best of our knowledge, this is the first reported case of coexisting fibrous dysplasia of overlying bone and VS as histopathological diagnosis. Wolters Kluwer - Medknow 2019-11-25 /pmc/articles/PMC6896621/ /pubmed/31903382 http://dx.doi.org/10.4103/ajns.AJNS_73_19 Text en Copyright: © 2019 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Sharma, Vikas
Kedia, Rishabh
Mohapatra, Ishani
Banerjee, Anirban Deep
Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence
title Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence
title_full Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence
title_fullStr Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence
title_full_unstemmed Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence
title_short Coexisting Vestibular Schwannoma with Fibrous Dysplasia: A Rare Occurrence
title_sort coexisting vestibular schwannoma with fibrous dysplasia: a rare occurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896621/
https://www.ncbi.nlm.nih.gov/pubmed/31903382
http://dx.doi.org/10.4103/ajns.AJNS_73_19
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