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Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome
Purpose. We present a case with Klippel-Trenaunay (KT) syndrome that had unilateral mature cataract and vitreoretinopathy. Case Report. A 17-year-old boy with KT syndrome presented to the clinic of ophthalmology for low vision in the right eye. His best corrected visual acuity (BCVA) was hand motion...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084616/ https://www.ncbi.nlm.nih.gov/pubmed/25031878 http://dx.doi.org/10.1155/2014/312030 |
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author | Olcaysu, Osman Okan Altun, Ahmet Olcaysu, Elif Marzıoğlu Ozdemır, Ebru Demır, Berrin |
author_facet | Olcaysu, Osman Okan Altun, Ahmet Olcaysu, Elif Marzıoğlu Ozdemır, Ebru Demır, Berrin |
author_sort | Olcaysu, Osman Okan |
collection | PubMed |
description | Purpose. We present a case with Klippel-Trenaunay (KT) syndrome that had unilateral mature cataract and vitreoretinopathy. Case Report. A 17-year-old boy with KT syndrome presented to the clinic of ophthalmology for low vision in the right eye. His best corrected visual acuity (BCVA) was hand motion in the right eye and 20/20 in the left eye. Anterior segment examination revealed mature cataract in the right. During the physical examination, port-wine stains were noted over right side of his face, ankle, and toes. He had asymmetric face and his head was larger on the right side. Leg lengths were symmetrical, although he had skin hypertrophy. Cranial magnetic resonance imaging studies showed cortical atrophy discordant to his age, asymmetric vascular dilatations in the right hemisphere, hypertrophy in the right periorbital soft tissue, and choroidal plexus. The patient received an uncomplicated cataract surgery. His BCVA in the right eye improved to 20/200 after the surgery. After removing cataractous lens, we were able to examine the fundus that revealed severe vitreoretinopathy and choroidal hemangioma. Conclusion. This case emphasizes the importance of prompt ophthalmic examination in patients with KT syndrome. |
format | Online Article Text |
id | pubmed-4084616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40846162014-07-16 Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome Olcaysu, Osman Okan Altun, Ahmet Olcaysu, Elif Marzıoğlu Ozdemır, Ebru Demır, Berrin Case Rep Ophthalmol Med Case Report Purpose. We present a case with Klippel-Trenaunay (KT) syndrome that had unilateral mature cataract and vitreoretinopathy. Case Report. A 17-year-old boy with KT syndrome presented to the clinic of ophthalmology for low vision in the right eye. His best corrected visual acuity (BCVA) was hand motion in the right eye and 20/20 in the left eye. Anterior segment examination revealed mature cataract in the right. During the physical examination, port-wine stains were noted over right side of his face, ankle, and toes. He had asymmetric face and his head was larger on the right side. Leg lengths were symmetrical, although he had skin hypertrophy. Cranial magnetic resonance imaging studies showed cortical atrophy discordant to his age, asymmetric vascular dilatations in the right hemisphere, hypertrophy in the right periorbital soft tissue, and choroidal plexus. The patient received an uncomplicated cataract surgery. His BCVA in the right eye improved to 20/200 after the surgery. After removing cataractous lens, we were able to examine the fundus that revealed severe vitreoretinopathy and choroidal hemangioma. Conclusion. This case emphasizes the importance of prompt ophthalmic examination in patients with KT syndrome. Hindawi Publishing Corporation 2014 2014-06-16 /pmc/articles/PMC4084616/ /pubmed/25031878 http://dx.doi.org/10.1155/2014/312030 Text en Copyright © 2014 Osman Okan Olcaysu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Olcaysu, Osman Okan Altun, Ahmet Olcaysu, Elif Marzıoğlu Ozdemır, Ebru Demır, Berrin Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome |
title | Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome |
title_full | Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome |
title_fullStr | Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome |
title_full_unstemmed | Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome |
title_short | Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome |
title_sort | unilateral cataract and vitreoretinopathy in a case with klippel-trenaunay syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084616/ https://www.ncbi.nlm.nih.gov/pubmed/25031878 http://dx.doi.org/10.1155/2014/312030 |
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