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Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady
INTRODUCTION: Hyphema and orbital apex syndrome occurring concurrently in a patient with herpes zoster ophthalmicus have not been reported previously. We present a case with these unique findings and discuss the pathogenesis of these conditions and their management. PRESENTATION OF CASE: A 59-year-o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219611/ https://www.ncbi.nlm.nih.gov/pubmed/28061417 http://dx.doi.org/10.1016/j.ijscr.2016.12.010 |
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author | Othman, Khairuddin Evelyn-Tai, Li Min Raja-Azmi, Mohd Noor Julieana, Muhammed Liza-Sharmini, Ahmad Tajudin Tharakan, John Besari, Alwi Muhd Zunaina, Embong Shatriah, Ismail |
author_facet | Othman, Khairuddin Evelyn-Tai, Li Min Raja-Azmi, Mohd Noor Julieana, Muhammed Liza-Sharmini, Ahmad Tajudin Tharakan, John Besari, Alwi Muhd Zunaina, Embong Shatriah, Ismail |
author_sort | Othman, Khairuddin |
collection | PubMed |
description | INTRODUCTION: Hyphema and orbital apex syndrome occurring concurrently in a patient with herpes zoster ophthalmicus have not been reported previously. We present a case with these unique findings and discuss the pathogenesis of these conditions and their management. PRESENTATION OF CASE: A 59-year-old Malay lady with underlying diabetes mellitus presented with manifestations of zoster ophthalmicus in the left eye. Two weeks later, she developed total hyphema, and complete ophthalmoplegia suggestive of orbital apex syndrome. She was treated with combination of intravenous acyclovir and oral corticosteroids, and regained full recovery of ocular motility. Total hyphema persisted, and she required surgical intervention. DISCUSSION: Hyphema is postulated to occur due to an immune vasculitis affecting the iris vessels. Orbital apex syndrome is probably due to an occlusive vasculitis affecting the vasculature of the extraocular muscles and optic nerve, resulting from a direct invasion by varicella zoster virus or infiltration of perivascular inflammatory cells. Magnetic Resonance Imaging of the brain is essential to exclude possibility of local causes at the orbital apex area. CONCLUSION: Herpes zoster ophthalmicus is an uncommon ocular presentation. Managing two concurrent complications; persistent total hyphema and orbital apex syndrome is a challenging clinical situation. Early diagnosis and prompt treatment are essential to prevent potential blinding situation. |
format | Online Article Text |
id | pubmed-5219611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-52196112017-01-09 Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady Othman, Khairuddin Evelyn-Tai, Li Min Raja-Azmi, Mohd Noor Julieana, Muhammed Liza-Sharmini, Ahmad Tajudin Tharakan, John Besari, Alwi Muhd Zunaina, Embong Shatriah, Ismail Int J Surg Case Rep Case Report INTRODUCTION: Hyphema and orbital apex syndrome occurring concurrently in a patient with herpes zoster ophthalmicus have not been reported previously. We present a case with these unique findings and discuss the pathogenesis of these conditions and their management. PRESENTATION OF CASE: A 59-year-old Malay lady with underlying diabetes mellitus presented with manifestations of zoster ophthalmicus in the left eye. Two weeks later, she developed total hyphema, and complete ophthalmoplegia suggestive of orbital apex syndrome. She was treated with combination of intravenous acyclovir and oral corticosteroids, and regained full recovery of ocular motility. Total hyphema persisted, and she required surgical intervention. DISCUSSION: Hyphema is postulated to occur due to an immune vasculitis affecting the iris vessels. Orbital apex syndrome is probably due to an occlusive vasculitis affecting the vasculature of the extraocular muscles and optic nerve, resulting from a direct invasion by varicella zoster virus or infiltration of perivascular inflammatory cells. Magnetic Resonance Imaging of the brain is essential to exclude possibility of local causes at the orbital apex area. CONCLUSION: Herpes zoster ophthalmicus is an uncommon ocular presentation. Managing two concurrent complications; persistent total hyphema and orbital apex syndrome is a challenging clinical situation. Early diagnosis and prompt treatment are essential to prevent potential blinding situation. Elsevier 2016-12-21 /pmc/articles/PMC5219611/ /pubmed/28061417 http://dx.doi.org/10.1016/j.ijscr.2016.12.010 Text en © 2016 The Authors 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 Othman, Khairuddin Evelyn-Tai, Li Min Raja-Azmi, Mohd Noor Julieana, Muhammed Liza-Sharmini, Ahmad Tajudin Tharakan, John Besari, Alwi Muhd Zunaina, Embong Shatriah, Ismail Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
title | Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
title_full | Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
title_fullStr | Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
title_full_unstemmed | Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
title_short | Concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
title_sort | concurrent hyphema and orbital apex syndrome following herpes zoster ophthalmicus in a middle aged lady |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219611/ https://www.ncbi.nlm.nih.gov/pubmed/28061417 http://dx.doi.org/10.1016/j.ijscr.2016.12.010 |
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