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Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos
In this case report we describe a 27-year-old man who presented with progressive enophthalmos for 5 months without any other associated ocular symptoms such as pain, diplopia, or visual disturbance. Computed tomography showed that his progressive enophthalmos originated from a frontoethmoidal mucoce...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Ophthalmological Society
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364434/ https://www.ncbi.nlm.nih.gov/pubmed/22670079 http://dx.doi.org/10.3341/kjo.2012.26.3.212 |
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author | Paik, Ji-Sun Kim, Su-Whan Yang, Suk-Woo |
author_facet | Paik, Ji-Sun Kim, Su-Whan Yang, Suk-Woo |
author_sort | Paik, Ji-Sun |
collection | PubMed |
description | In this case report we describe a 27-year-old man who presented with progressive enophthalmos for 5 months without any other associated ocular symptoms such as pain, diplopia, or visual disturbance. Computed tomography showed that his progressive enophthalmos originated from a frontoethmoidal mucocele and this caused destruction of the lamina papyracea and shrinkage of the ethmoidal air cell. Finally the enlarged orbital space caused an inward deviation of the eyeball. Endoscopic marsupialization was successfully performed by an otolaryngologist and did not result in any ophthalmologic sequelae. Although frontoethmoidal sinus mucoceles mostly frequently originates from orbital mucoceles, enophthalmic manifestations are very rare. Enophthalmic conditions are not as responsive to surgical interventions as exophthalmic conditions. |
format | Online Article Text |
id | pubmed-3364434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Ophthalmological Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-33644342012-06-06 Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos Paik, Ji-Sun Kim, Su-Whan Yang, Suk-Woo Korean J Ophthalmol Case Report In this case report we describe a 27-year-old man who presented with progressive enophthalmos for 5 months without any other associated ocular symptoms such as pain, diplopia, or visual disturbance. Computed tomography showed that his progressive enophthalmos originated from a frontoethmoidal mucocele and this caused destruction of the lamina papyracea and shrinkage of the ethmoidal air cell. Finally the enlarged orbital space caused an inward deviation of the eyeball. Endoscopic marsupialization was successfully performed by an otolaryngologist and did not result in any ophthalmologic sequelae. Although frontoethmoidal sinus mucoceles mostly frequently originates from orbital mucoceles, enophthalmic manifestations are very rare. Enophthalmic conditions are not as responsive to surgical interventions as exophthalmic conditions. The Korean Ophthalmological Society 2012-06 2012-05-22 /pmc/articles/PMC3364434/ /pubmed/22670079 http://dx.doi.org/10.3341/kjo.2012.26.3.212 Text en © 2012 The Korean Ophthalmological Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Paik, Ji-Sun Kim, Su-Whan Yang, Suk-Woo Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos |
title | Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos |
title_full | Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos |
title_fullStr | Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos |
title_full_unstemmed | Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos |
title_short | Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos |
title_sort | frontoethmoidal mucocele presenting as progressive enophthalmos |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364434/ https://www.ncbi.nlm.nih.gov/pubmed/22670079 http://dx.doi.org/10.3341/kjo.2012.26.3.212 |
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