Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature - A Solitary fibrous tumor in the orbit

dc.contributor.author Ali, Mohammad Javed
dc.contributor.author Honavar, Santosh G.
dc.contributor.author Naik, Milind N.
dc.contributor.author Vemuganti, Geeta K.
dc.date.accessioned 2022-03-27T04:11:43Z
dc.date.available 2022-03-27T04:11:43Z
dc.date.issued 2013-08-12
dc.description.abstract 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.
dc.identifier.citation Journal of Research in Medical Sciences. v.18(6)
dc.identifier.issn 17351995
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/6798
dc.subject BCL-2
dc.subject CD34
dc.subject Hemangiopericytoma
dc.subject Orbit
dc.subject Solitary fibrous tumor
dc.title Orbital solitary fibrous tumor: A rare clinicopathologic correlation and review of literature - A Solitary fibrous tumor in the orbit
dc.type Journal. Article
dspace.entity.type
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