Orbital Apex Syndrome in Herpes Zoster Ophthalmicus
Orbital apex syndrome is a rare manifestation of Herpes Zoster Ophthalmicus. Herein we report on a case of orbital apex syndrome secondary to Herpes Zoster Ophthalmicus. A 75 year-old male complained of vision loss, conjunctival hyperemia and proptosis on the left eye, was referred to our clinic. V...
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2012-01-01
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Online Access: | http://dx.doi.org/10.1155/2012/854503 |
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doaj-dd976648d18b4ff3b08d9bc836f0d5cf2020-11-24T20:59:12ZengHindawi LimitedCase Reports in Ophthalmological Medicine2090-67222090-67302012-01-01201210.1155/2012/854503854503Orbital Apex Syndrome in Herpes Zoster OphthalmicusHatice Arda0Ertugrul Mirza1Koray Gumus2Ayse Oner3Sarper Karakucuk4Ender Sırakaya5Department of Ophthalmology, Medical Faculty Erciyes University, 38039 Kayseri, TurkeyDepartment of Ophthalmology, Medical Faculty Erciyes University, 38039 Kayseri, TurkeyDepartment of Ophthalmology, Medical Faculty Erciyes University, 38039 Kayseri, TurkeyDepartment of Ophthalmology, Medical Faculty Erciyes University, 38039 Kayseri, TurkeyDepartment of Ophthalmology, Medical Faculty Erciyes University, 38039 Kayseri, TurkeyDepartment of Ophthalmology, Medical Faculty Erciyes University, 38039 Kayseri, TurkeyOrbital apex syndrome is a rare manifestation of Herpes Zoster Ophthalmicus. Herein we report on a case of orbital apex syndrome secondary to Herpes Zoster Ophthalmicus. A 75 year-old male complained of vision loss, conjunctival hyperemia and proptosis on the left eye, was referred to our clinic. Visual acuity was 5/10 Snellen lines and he had conjunctival hyperemia, chemosis, minimal nuclear cataract and proptosis on the left eye. A diagnosis of orbital pseudotumor was demonstrated firstly. The patient received oral and topical corticosteroids, antiinflammatory and antibiotic agents. On day 2, vesiculopustular lesions were observed, Herpes Zoster Ophthalmicus was diagnosed and corticosteroid treatment stopped, oral acyclovir treatment initiated. Two days later, total ophthalmoplegia, ptosis and significant visual loss were observed on the left. The diagnosis of orbital apex syndrome was considered and the patient commenced on an intravenous acyclovir treatment. After the improvement of acute symptoms, a tapering dose of oral cortisone treatment initiated to accelarate the recovery of ophthalmoplegia. At 5-month follow-up, ptosis and ocular motility showed improvement. VA did not significantly improve because of cataract and choroidal detachment on the left. We conclude that ophthalmoplegia secondary to Herpes Zoster Ophthalmicus responds favourably to intravenous acyclovir and steroids.http://dx.doi.org/10.1155/2012/854503 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hatice Arda Ertugrul Mirza Koray Gumus Ayse Oner Sarper Karakucuk Ender Sırakaya |
spellingShingle |
Hatice Arda Ertugrul Mirza Koray Gumus Ayse Oner Sarper Karakucuk Ender Sırakaya Orbital Apex Syndrome in Herpes Zoster Ophthalmicus Case Reports in Ophthalmological Medicine |
author_facet |
Hatice Arda Ertugrul Mirza Koray Gumus Ayse Oner Sarper Karakucuk Ender Sırakaya |
author_sort |
Hatice Arda |
title |
Orbital Apex Syndrome in Herpes Zoster Ophthalmicus |
title_short |
Orbital Apex Syndrome in Herpes Zoster Ophthalmicus |
title_full |
Orbital Apex Syndrome in Herpes Zoster Ophthalmicus |
title_fullStr |
Orbital Apex Syndrome in Herpes Zoster Ophthalmicus |
title_full_unstemmed |
Orbital Apex Syndrome in Herpes Zoster Ophthalmicus |
title_sort |
orbital apex syndrome in herpes zoster ophthalmicus |
publisher |
Hindawi Limited |
series |
Case Reports in Ophthalmological Medicine |
issn |
2090-6722 2090-6730 |
publishDate |
2012-01-01 |
description |
Orbital apex syndrome is a rare manifestation of Herpes Zoster Ophthalmicus. Herein we report on a case of orbital apex syndrome secondary to Herpes Zoster Ophthalmicus. A 75 year-old male complained of vision loss, conjunctival hyperemia and proptosis on the left eye, was referred to our clinic. Visual acuity was 5/10 Snellen lines and he had conjunctival hyperemia, chemosis, minimal nuclear cataract and proptosis on the left eye. A diagnosis of orbital pseudotumor was demonstrated firstly. The patient received oral and topical corticosteroids, antiinflammatory and antibiotic agents. On day 2, vesiculopustular lesions were observed, Herpes Zoster Ophthalmicus was diagnosed and corticosteroid treatment stopped, oral acyclovir treatment initiated. Two days later, total ophthalmoplegia, ptosis and significant visual loss were observed on the left. The diagnosis of orbital apex syndrome was considered and the patient commenced on an intravenous acyclovir treatment. After the improvement of acute symptoms, a tapering dose of oral cortisone treatment initiated to accelarate the recovery of ophthalmoplegia. At 5-month follow-up, ptosis and ocular motility showed improvement. VA did not significantly improve because of cataract and choroidal detachment on the left. We conclude that ophthalmoplegia secondary to Herpes Zoster Ophthalmicus responds favourably to intravenous acyclovir and steroids. |
url |
http://dx.doi.org/10.1155/2012/854503 |
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