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Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report

Bilateral Idiopathic Orbital Inflammation Syndrome (IOIS) is rare in adults. Most commonly it affects the young adults and children. It is mostly unilateral condition. This is a case of 50 years old male coming with the complaints of painless proptosis on both the eyes for 1 year. The history of dip...

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Autor principal: Sarkar, Sandip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300788/
https://www.ncbi.nlm.nih.gov/pubmed/30581306
http://dx.doi.org/10.1016/j.sjopt.2018.03.007
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author Sarkar, Sandip
author_facet Sarkar, Sandip
author_sort Sarkar, Sandip
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description Bilateral Idiopathic Orbital Inflammation Syndrome (IOIS) is rare in adults. Most commonly it affects the young adults and children. It is mostly unilateral condition. This is a case of 50 years old male coming with the complaints of painless proptosis on both the eyes for 1 year. The history of diplopia was also found. On examination, it was found that there was restriction of movements in Right eye superiorly. Any history of associated systemic illness was not found. Based on the clinical examination, laboratory reports and contrast enhanced computed tomography (CECT) the diagnosis of Bilateral IOIS was made. Patient was treated with Intravenous methyl prednisolone followed by oral Prednisolone in tapering doses for a period of 2 months. After 2 month of regular follow up the patient was found to have a favorable outcome with improved visual acuity and reduction in the size of the proptosed eye. Patient was followed up for another 6 month to observe any recurrence or relapse.
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spelling pubmed-63007882018-12-21 Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report Sarkar, Sandip Saudi J Ophthalmol Case Report Bilateral Idiopathic Orbital Inflammation Syndrome (IOIS) is rare in adults. Most commonly it affects the young adults and children. It is mostly unilateral condition. This is a case of 50 years old male coming with the complaints of painless proptosis on both the eyes for 1 year. The history of diplopia was also found. On examination, it was found that there was restriction of movements in Right eye superiorly. Any history of associated systemic illness was not found. Based on the clinical examination, laboratory reports and contrast enhanced computed tomography (CECT) the diagnosis of Bilateral IOIS was made. Patient was treated with Intravenous methyl prednisolone followed by oral Prednisolone in tapering doses for a period of 2 months. After 2 month of regular follow up the patient was found to have a favorable outcome with improved visual acuity and reduction in the size of the proptosed eye. Patient was followed up for another 6 month to observe any recurrence or relapse. Elsevier 2018 2018-04-13 /pmc/articles/PMC6300788/ /pubmed/30581306 http://dx.doi.org/10.1016/j.sjopt.2018.03.007 Text en © 2018 The Author http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Sarkar, Sandip
Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report
title Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report
title_full Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report
title_fullStr Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report
title_full_unstemmed Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report
title_short Bilateral Idiopathic Orbital Inflammation Syndrome in an adult patient: A rare case report
title_sort bilateral idiopathic orbital inflammation syndrome in an adult patient: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300788/
https://www.ncbi.nlm.nih.gov/pubmed/30581306
http://dx.doi.org/10.1016/j.sjopt.2018.03.007
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