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Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature

Orbital solitary fibrous tumor (SFT) is a rare tumor and orbits are a very uncommon site. It is mostly noted to arise from mesenchymal structures like pleura and peritoneum. The diagnosis of orbital SFT cannot be made with certainty on clinical or radiological evaluation alone and requires immunohis...

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Autores principales: Ali, Mohammad Javed, Honavar, Santosh G., Naik, Milind N., Vemuganti, Geeta K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818628/
https://www.ncbi.nlm.nih.gov/pubmed/24250707
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author Ali, Mohammad Javed
Honavar, Santosh G.
Naik, Milind N.
Vemuganti, Geeta K.
author_facet Ali, Mohammad Javed
Honavar, Santosh G.
Naik, Milind N.
Vemuganti, Geeta K.
author_sort Ali, Mohammad Javed
collection PubMed
description Orbital solitary fibrous tumor (SFT) is a rare tumor and orbits are a very uncommon site. It is mostly noted to arise from mesenchymal structures like pleura and peritoneum. The diagnosis of orbital SFT cannot be made with certainty on clinical or radiological evaluation alone and requires immunohistochemical studies for confirmation. Orbital SFT's usually show an indolent clinical course and a complete cure can usually be achieved with complete resection. We describe clinical presentations, radiological and operative findings, and pathological features of a patient with orbital SFT along with a brief review of literature.
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spelling pubmed-38186282013-11-18 Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature Ali, Mohammad Javed Honavar, Santosh G. Naik, Milind N. Vemuganti, Geeta K. J Res Med Sci Case Report Orbital solitary fibrous tumor (SFT) is a rare tumor and orbits are a very uncommon site. It is mostly noted to arise from mesenchymal structures like pleura and peritoneum. The diagnosis of orbital SFT cannot be made with certainty on clinical or radiological evaluation alone and requires immunohistochemical studies for confirmation. Orbital SFT's usually show an indolent clinical course and a complete cure can usually be achieved with complete resection. We describe clinical presentations, radiological and operative findings, and pathological features of a patient with orbital SFT along with a brief review of literature. Medknow Publications & Media Pvt Ltd 2013-06 /pmc/articles/PMC3818628/ /pubmed/24250707 Text en Copyright: © Journal of Research in Medical Sciences 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ali, Mohammad Javed
Honavar, Santosh G.
Naik, Milind N.
Vemuganti, Geeta K.
Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature
title Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature
title_full Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature
title_fullStr Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature
title_full_unstemmed Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature
title_short Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature
title_sort orbital solitary fibrous tumor: a rare clinicopathologic correlation and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818628/
https://www.ncbi.nlm.nih.gov/pubmed/24250707
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