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Orbital Chondroma: A rare mesenchymal tumor of orbit

While relatively common in the skeletal system, cartilaginous tumors are rarely seen originating from the orbit. Here, we report a rare case of an orbital chondroma. A 27-year-old male patient presented with a painless hard mass in the superonasal quadrant (SNQ) of left orbit since 3 months. On exam...

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Autores principales: Kabra, Ruchi S, Patel, Sonal B, Shanbhag, Swapna S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550997/
https://www.ncbi.nlm.nih.gov/pubmed/26265654
http://dx.doi.org/10.4103/0301-4738.162638
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author Kabra, Ruchi S
Patel, Sonal B
Shanbhag, Swapna S
author_facet Kabra, Ruchi S
Patel, Sonal B
Shanbhag, Swapna S
author_sort Kabra, Ruchi S
collection PubMed
description While relatively common in the skeletal system, cartilaginous tumors are rarely seen originating from the orbit. Here, we report a rare case of an orbital chondroma. A 27-year-old male patient presented with a painless hard mass in the superonasal quadrant (SNQ) of left orbit since 3 months. On examination, best-corrected visual acuity of both eyes was 20/20, with normal anterior and posterior segment with full movements of eyeballs and normal intraocular pressure. Computerized tomography scan revealed well defined soft tissue density lesion in SNQ of left orbit. Patient was operated for anteromedial orbitotomy under general anesthesia. Mass was excised intact and sent for histopathological examination (HPE). HPE report showed lobular aggregates of benign cartilaginous cells with mild atypia suggesting of benign cartilaginous tumor - chondroma. Very few cases of orbital chondroma have been reported in literature so far.
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spelling pubmed-45509972015-09-14 Orbital Chondroma: A rare mesenchymal tumor of orbit Kabra, Ruchi S Patel, Sonal B Shanbhag, Swapna S Indian J Ophthalmol Brief Communications While relatively common in the skeletal system, cartilaginous tumors are rarely seen originating from the orbit. Here, we report a rare case of an orbital chondroma. A 27-year-old male patient presented with a painless hard mass in the superonasal quadrant (SNQ) of left orbit since 3 months. On examination, best-corrected visual acuity of both eyes was 20/20, with normal anterior and posterior segment with full movements of eyeballs and normal intraocular pressure. Computerized tomography scan revealed well defined soft tissue density lesion in SNQ of left orbit. Patient was operated for anteromedial orbitotomy under general anesthesia. Mass was excised intact and sent for histopathological examination (HPE). HPE report showed lobular aggregates of benign cartilaginous cells with mild atypia suggesting of benign cartilaginous tumor - chondroma. Very few cases of orbital chondroma have been reported in literature so far. Medknow Publications & Media Pvt Ltd 2015-06 /pmc/articles/PMC4550997/ /pubmed/26265654 http://dx.doi.org/10.4103/0301-4738.162638 Text en Copyright: © Indian Journal of Ophthalmology 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 Brief Communications
Kabra, Ruchi S
Patel, Sonal B
Shanbhag, Swapna S
Orbital Chondroma: A rare mesenchymal tumor of orbit
title Orbital Chondroma: A rare mesenchymal tumor of orbit
title_full Orbital Chondroma: A rare mesenchymal tumor of orbit
title_fullStr Orbital Chondroma: A rare mesenchymal tumor of orbit
title_full_unstemmed Orbital Chondroma: A rare mesenchymal tumor of orbit
title_short Orbital Chondroma: A rare mesenchymal tumor of orbit
title_sort orbital chondroma: a rare mesenchymal tumor of orbit
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550997/
https://www.ncbi.nlm.nih.gov/pubmed/26265654
http://dx.doi.org/10.4103/0301-4738.162638
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