Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review
Purpose: To report a case of advanced childhood glaucoma secondary to congenital ectropion uveae (CEU). Case Report: The patient was a seven-year-old boy with unilateral glaucoma secondary to CEU and facial asymmetry, mild unilateral ptosis, and proptosis in the left eye. The intraocular press...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Knowledge E
2019-07-01
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Series: | Journal of Ophthalmic & Vision Research |
Online Access: | https://doi.org/10.18502/jovr.v14i3.4793 |
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author | Mohammadmehdi Hatami Azadeh Doozandeh Mohadeseh Feizi |
author_facet | Mohammadmehdi Hatami Azadeh Doozandeh Mohadeseh Feizi |
author_sort | Mohammadmehdi Hatami |
collection | DOAJ |
description | Purpose: To report a case of advanced childhood glaucoma secondary to congenital ectropion uveae (CEU).
Case Report: The patient was a seven-year-old boy with unilateral glaucoma secondary to CEU and facial asymmetry, mild unilateral ptosis, and proptosis in the left eye. The intraocular pressure (IOP) was 28 mmHg and cup-to-disc ratio was 0.8 in the left eye. After starting glaucoma medication, IOP decreased to 21 mmHg. In view of the uncontrolled IOP with medication and high cup-to-disc ratio and increased axial length of the left eye, mitomycin-C (MMC)-augmented trabeculectomy was planned. Despite sub-tenon MMC injection and bleb needling, the bleb failed after six months, and we had to perform a shunt procedure to control the IOP.
Conclusion: Although CEU is rare, ophthalmologists should be familiar with this syndrome because of the high frequency of glaucoma and its challenging management during childhood. |
first_indexed | 2024-04-13T13:58:28Z |
format | Article |
id | doaj.art-2acf5f5fd7744e5d9c4208f9bb032a07 |
institution | Directory Open Access Journal |
issn | 2008-322X |
language | English |
last_indexed | 2024-04-13T13:58:28Z |
publishDate | 2019-07-01 |
publisher | Knowledge E |
record_format | Article |
series | Journal of Ophthalmic & Vision Research |
spelling | doaj.art-2acf5f5fd7744e5d9c4208f9bb032a072022-12-22T02:44:06ZengKnowledge EJournal of Ophthalmic & Vision Research2008-322X2019-07-01141610.18502/jovr.v14i3.4793jovr.v14i3.4793Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature ReviewMohammadmehdi HatamiAzadeh DoozandehMohadeseh FeiziPurpose: To report a case of advanced childhood glaucoma secondary to congenital ectropion uveae (CEU). Case Report: The patient was a seven-year-old boy with unilateral glaucoma secondary to CEU and facial asymmetry, mild unilateral ptosis, and proptosis in the left eye. The intraocular pressure (IOP) was 28 mmHg and cup-to-disc ratio was 0.8 in the left eye. After starting glaucoma medication, IOP decreased to 21 mmHg. In view of the uncontrolled IOP with medication and high cup-to-disc ratio and increased axial length of the left eye, mitomycin-C (MMC)-augmented trabeculectomy was planned. Despite sub-tenon MMC injection and bleb needling, the bleb failed after six months, and we had to perform a shunt procedure to control the IOP. Conclusion: Although CEU is rare, ophthalmologists should be familiar with this syndrome because of the high frequency of glaucoma and its challenging management during childhood.https://doi.org/10.18502/jovr.v14i3.4793 |
spellingShingle | Mohammadmehdi Hatami Azadeh Doozandeh Mohadeseh Feizi Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review Journal of Ophthalmic & Vision Research |
title | Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review |
title_full | Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review |
title_fullStr | Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review |
title_full_unstemmed | Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review |
title_short | Glaucoma in Ectropion Uveae Syndrome: A Case Report and Literature Review |
title_sort | glaucoma in ectropion uveae syndrome a case report and literature review |
url | https://doi.org/10.18502/jovr.v14i3.4793 |
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