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Congenital intrascleral cyst

Congenital intrascleral cysts are rare. They are mostly located at the limbus with corneal involvement. We report a case of a 30-month-old boy with a bulber conjunctival cyst noticed at birth. The lesion enlarged over the following months but did not involve the cornea. During surgery the cyst prove...

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Detalles Bibliográficos
Autores principales: Akbaba, Müslime, Hacıyakupoğlu, Gülhanım, Uğuz, Aysun, Karslıoğlu, Şafak, Karcıoğlu, Zeynel
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102589/
https://www.ncbi.nlm.nih.gov/pubmed/21654885
http://dx.doi.org/10.2147/OPTH.S19789
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author Akbaba, Müslime
Hacıyakupoğlu, Gülhanım
Uğuz, Aysun
Karslıoğlu, Şafak
Karcıoğlu, Zeynel
author_facet Akbaba, Müslime
Hacıyakupoğlu, Gülhanım
Uğuz, Aysun
Karslıoğlu, Şafak
Karcıoğlu, Zeynel
author_sort Akbaba, Müslime
collection PubMed
description Congenital intrascleral cysts are rare. They are mostly located at the limbus with corneal involvement. We report a case of a 30-month-old boy with a bulber conjunctival cyst noticed at birth. The lesion enlarged over the following months but did not involve the cornea. During surgery the cyst proved to be intrascleral and a complete excision was carried out. The remaining defect was repaired with banked fascia lata. The histopathology revealed a scleral cyst wall lined by nonkeratinizing squamous epithelium with no goblet cells. We conclude that congenital intrascleral epithelial cysts are rare but should be considered in differential diagnosis of external eye cystic lesions. In our case, early excision and repair with fascia lata led to an uncomplicated postoperative course of 6 years.
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spelling pubmed-31025892011-06-07 Congenital intrascleral cyst Akbaba, Müslime Hacıyakupoğlu, Gülhanım Uğuz, Aysun Karslıoğlu, Şafak Karcıoğlu, Zeynel Clin Ophthalmol Case Report Congenital intrascleral cysts are rare. They are mostly located at the limbus with corneal involvement. We report a case of a 30-month-old boy with a bulber conjunctival cyst noticed at birth. The lesion enlarged over the following months but did not involve the cornea. During surgery the cyst proved to be intrascleral and a complete excision was carried out. The remaining defect was repaired with banked fascia lata. The histopathology revealed a scleral cyst wall lined by nonkeratinizing squamous epithelium with no goblet cells. We conclude that congenital intrascleral epithelial cysts are rare but should be considered in differential diagnosis of external eye cystic lesions. In our case, early excision and repair with fascia lata led to an uncomplicated postoperative course of 6 years. Dove Medical Press 2011 2011-05-13 /pmc/articles/PMC3102589/ /pubmed/21654885 http://dx.doi.org/10.2147/OPTH.S19789 Text en © 2011 Akbaba et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Case Report
Akbaba, Müslime
Hacıyakupoğlu, Gülhanım
Uğuz, Aysun
Karslıoğlu, Şafak
Karcıoğlu, Zeynel
Congenital intrascleral cyst
title Congenital intrascleral cyst
title_full Congenital intrascleral cyst
title_fullStr Congenital intrascleral cyst
title_full_unstemmed Congenital intrascleral cyst
title_short Congenital intrascleral cyst
title_sort congenital intrascleral cyst
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102589/
https://www.ncbi.nlm.nih.gov/pubmed/21654885
http://dx.doi.org/10.2147/OPTH.S19789
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