Granular Cell Tumor of the Orbit

Purpose: To report a case of granular cell tumor as a rare orbital pathology. Case report: A 50-year-old female presented with a 4-year history of diplopia, right ocular displacement and a firm nontender mass in her right lower lid. Computed tomography (CT) scan of the orbit disclosed a well-define...

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Main Authors: Hossein Salour, Mehdi Tavakoli, Saeed Karimi, Mohammad Faghihi
Format: Article
Language:English
Published: Knowledge E 2013-01-01
Series:Journal of Ophthalmic & Vision Research
Online Access:http://www.jovr.org/article.asp?issn=2008-322X;year=2013;volume=8;issue=4;spage=376;epage=379;aulast=Salour
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spelling doaj-eea9be69aeb84fedb217ba820e4a971f2020-11-24T22:06:36ZengKnowledge EJournal of Ophthalmic & Vision Research2008-322X2013-01-0184376379Granular Cell Tumor of the OrbitHossein SalourMehdi TavakoliSaeed KarimiMohammad FaghihiPurpose: To report a case of granular cell tumor as a rare orbital pathology. Case report: A 50-year-old female presented with a 4-year history of diplopia, right ocular displacement and a firm nontender mass in her right lower lid. Computed tomography (CT) scan of the orbit disclosed a well-defined mass in the right inferior orbit involving the right inferior rectus. Subtotal excision of the mass was performed, and histopathologic and immunohistochemical studies revealed granular cell tumor. Subsequently, the tumor recurred and exenteration was required as multiple sessions of radiotherapy failed to prevent the residual tumor from growing. Conclusion: Granular cell tumor, though very rare in the orbit, should be considered in patients with orbital masses especially in cases with involvement of the inferior rectus muscle. Infiltrative tumors may be impossible to completely resect and can rapidly recur following surgery.http://www.jovr.org/article.asp?issn=2008-322X;year=2013;volume=8;issue=4;spage=376;epage=379;aulast=Salour
collection DOAJ
language English
format Article
sources DOAJ
author Hossein Salour
Mehdi Tavakoli
Saeed Karimi
Mohammad Faghihi
spellingShingle Hossein Salour
Mehdi Tavakoli
Saeed Karimi
Mohammad Faghihi
Granular Cell Tumor of the Orbit
Journal of Ophthalmic & Vision Research
author_facet Hossein Salour
Mehdi Tavakoli
Saeed Karimi
Mohammad Faghihi
author_sort Hossein Salour
title Granular Cell Tumor of the Orbit
title_short Granular Cell Tumor of the Orbit
title_full Granular Cell Tumor of the Orbit
title_fullStr Granular Cell Tumor of the Orbit
title_full_unstemmed Granular Cell Tumor of the Orbit
title_sort granular cell tumor of the orbit
publisher Knowledge E
series Journal of Ophthalmic & Vision Research
issn 2008-322X
publishDate 2013-01-01
description Purpose: To report a case of granular cell tumor as a rare orbital pathology. Case report: A 50-year-old female presented with a 4-year history of diplopia, right ocular displacement and a firm nontender mass in her right lower lid. Computed tomography (CT) scan of the orbit disclosed a well-defined mass in the right inferior orbit involving the right inferior rectus. Subtotal excision of the mass was performed, and histopathologic and immunohistochemical studies revealed granular cell tumor. Subsequently, the tumor recurred and exenteration was required as multiple sessions of radiotherapy failed to prevent the residual tumor from growing. Conclusion: Granular cell tumor, though very rare in the orbit, should be considered in patients with orbital masses especially in cases with involvement of the inferior rectus muscle. Infiltrative tumors may be impossible to completely resect and can rapidly recur following surgery.
url http://www.jovr.org/article.asp?issn=2008-322X;year=2013;volume=8;issue=4;spage=376;epage=379;aulast=Salour
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AT mehditavakoli granularcelltumoroftheorbit
AT saeedkarimi granularcelltumoroftheorbit
AT mohammadfaghihi granularcelltumoroftheorbit
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