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Malignant solitary fibrous tumour of orbit
Solitary fibrous tumor (SFT) is a rare neoplasm that is thought to be of mesenchymal origin. Occurrence of such a tumor in the orbit is rare, more so in its malignant form. Histopathologically, it can mimic several other tumors of the orbit and can be differentiated by CD34 positivity. We report a c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379805/ https://www.ncbi.nlm.nih.gov/pubmed/28413534 http://dx.doi.org/10.4103/1793-5482.144180 |
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author | Chakrabartty, Hrishikesh Singhvi, Shashi Purohit, Devendra Mittal, Radhey Shyam |
author_facet | Chakrabartty, Hrishikesh Singhvi, Shashi Purohit, Devendra Mittal, Radhey Shyam |
author_sort | Chakrabartty, Hrishikesh |
collection | PubMed |
description | Solitary fibrous tumor (SFT) is a rare neoplasm that is thought to be of mesenchymal origin. Occurrence of such a tumor in the orbit is rare, more so in its malignant form. Histopathologically, it can mimic several other tumors of the orbit and can be differentiated by CD34 positivity. We report a case of malignant transformation of an SFT of the orbit that recurred after 15 years. The differentiating histopathological features with special stress on the importance of CD34 positivity and principles of management are outlined. The need for long-term follow-up to detect recurrence and malignancy is stressed. |
format | Online Article Text |
id | pubmed-5379805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53798052017-04-14 Malignant solitary fibrous tumour of orbit Chakrabartty, Hrishikesh Singhvi, Shashi Purohit, Devendra Mittal, Radhey Shyam Asian J Neurosurg Case Report Solitary fibrous tumor (SFT) is a rare neoplasm that is thought to be of mesenchymal origin. Occurrence of such a tumor in the orbit is rare, more so in its malignant form. Histopathologically, it can mimic several other tumors of the orbit and can be differentiated by CD34 positivity. We report a case of malignant transformation of an SFT of the orbit that recurred after 15 years. The differentiating histopathological features with special stress on the importance of CD34 positivity and principles of management are outlined. The need for long-term follow-up to detect recurrence and malignancy is stressed. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5379805/ /pubmed/28413534 http://dx.doi.org/10.4103/1793-5482.144180 Text en Copyright: © 2014 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Chakrabartty, Hrishikesh Singhvi, Shashi Purohit, Devendra Mittal, Radhey Shyam Malignant solitary fibrous tumour of orbit |
title | Malignant solitary fibrous tumour of orbit |
title_full | Malignant solitary fibrous tumour of orbit |
title_fullStr | Malignant solitary fibrous tumour of orbit |
title_full_unstemmed | Malignant solitary fibrous tumour of orbit |
title_short | Malignant solitary fibrous tumour of orbit |
title_sort | malignant solitary fibrous tumour of orbit |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379805/ https://www.ncbi.nlm.nih.gov/pubmed/28413534 http://dx.doi.org/10.4103/1793-5482.144180 |
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