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Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment

Wyburn–Mason syndrome is associated with unilateral retinal racemose hemangioma. Rarely, it presents with bilateral and symmetrical grade of malformation. We describe a 37-year old male, who presented with Wyburn–Mason syndrome presenting with bilateral but asymmetrical retinal hemangioma. The eye w...

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Autores principales: Pangtey, Bhanu P S, Kohli, Piyush, Ramasamy, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256888/
https://www.ncbi.nlm.nih.gov/pubmed/30451208
http://dx.doi.org/10.4103/ijo.IJO_455_18
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author Pangtey, Bhanu P S
Kohli, Piyush
Ramasamy, Kim
author_facet Pangtey, Bhanu P S
Kohli, Piyush
Ramasamy, Kim
author_sort Pangtey, Bhanu P S
collection PubMed
description Wyburn–Mason syndrome is associated with unilateral retinal racemose hemangioma. Rarely, it presents with bilateral and symmetrical grade of malformation. We describe a 37-year old male, who presented with Wyburn–Mason syndrome presenting with bilateral but asymmetrical retinal hemangioma. The eye with advanced grade of hemangioma was complicated with exudation, intraretinal fluid, neurosensory detachment, and reduced vision. He was treated with one intravitreal injection of bevacizumab, after which both the intraretinal fluid and neurosensory detachment resolved. His vision improved and was maintained till 1 year of follow-up.
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spelling pubmed-62568882018-12-15 Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment Pangtey, Bhanu P S Kohli, Piyush Ramasamy, Kim Indian J Ophthalmol Case Reports Wyburn–Mason syndrome is associated with unilateral retinal racemose hemangioma. Rarely, it presents with bilateral and symmetrical grade of malformation. We describe a 37-year old male, who presented with Wyburn–Mason syndrome presenting with bilateral but asymmetrical retinal hemangioma. The eye with advanced grade of hemangioma was complicated with exudation, intraretinal fluid, neurosensory detachment, and reduced vision. He was treated with one intravitreal injection of bevacizumab, after which both the intraretinal fluid and neurosensory detachment resolved. His vision improved and was maintained till 1 year of follow-up. Medknow Publications & Media Pvt Ltd 2018-12 /pmc/articles/PMC6256888/ /pubmed/30451208 http://dx.doi.org/10.4103/ijo.IJO_455_18 Text en Copyright: © 2018 Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Reports
Pangtey, Bhanu P S
Kohli, Piyush
Ramasamy, Kim
Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
title Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
title_full Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
title_fullStr Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
title_full_unstemmed Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
title_short Wyburn–Mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
title_sort wyburn–mason syndrome presenting with bilateral retinal racemose hemangioma with unilateral serous retinal detachment
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256888/
https://www.ncbi.nlm.nih.gov/pubmed/30451208
http://dx.doi.org/10.4103/ijo.IJO_455_18
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