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Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report
We present a very rare case of torpedo maculopathy (TM) with multifocal central serous chorioretinopathy. A 26-year-old male presented with painless loss of vision in the right eye of 2 months duration. Clinical examination showed a torpedo-shaped lesion temporal to fovea and subretinal fluid in fov...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819134/ https://www.ncbi.nlm.nih.gov/pubmed/29380797 http://dx.doi.org/10.4103/ijo.IJO_812_17 |
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author | Panigrahi, Pradeep Kumar Minj, Anita Satapathy, Jasmita |
author_facet | Panigrahi, Pradeep Kumar Minj, Anita Satapathy, Jasmita |
author_sort | Panigrahi, Pradeep Kumar |
collection | PubMed |
description | We present a very rare case of torpedo maculopathy (TM) with multifocal central serous chorioretinopathy. A 26-year-old male presented with painless loss of vision in the right eye of 2 months duration. Clinical examination showed a torpedo-shaped lesion temporal to fovea and subretinal fluid in foveal center. Fluorescein angiography showed multifocal leaks. Optical coherence tomography showed an optically clear space/neurosensory detachment at the site of lesion. Patient underwent focal laser to the leaks. TM is a rare congenital disorder detected accidentally during routine fundus examination. It is usually unilateral and does not affect vision. |
format | Online Article Text |
id | pubmed-5819134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58191342018-02-22 Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report Panigrahi, Pradeep Kumar Minj, Anita Satapathy, Jasmita Indian J Ophthalmol Case Report We present a very rare case of torpedo maculopathy (TM) with multifocal central serous chorioretinopathy. A 26-year-old male presented with painless loss of vision in the right eye of 2 months duration. Clinical examination showed a torpedo-shaped lesion temporal to fovea and subretinal fluid in foveal center. Fluorescein angiography showed multifocal leaks. Optical coherence tomography showed an optically clear space/neurosensory detachment at the site of lesion. Patient underwent focal laser to the leaks. TM is a rare congenital disorder detected accidentally during routine fundus examination. It is usually unilateral and does not affect vision. Medknow Publications & Media Pvt Ltd 2018-02 /pmc/articles/PMC5819134/ /pubmed/29380797 http://dx.doi.org/10.4103/ijo.IJO_812_17 Text en Copyright: © 2018 Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Panigrahi, Pradeep Kumar Minj, Anita Satapathy, Jasmita Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report |
title | Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report |
title_full | Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report |
title_fullStr | Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report |
title_full_unstemmed | Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report |
title_short | Torpedo maculopathy with multifocal central serous chorioretinopathy: A rare case report |
title_sort | torpedo maculopathy with multifocal central serous chorioretinopathy: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819134/ https://www.ncbi.nlm.nih.gov/pubmed/29380797 http://dx.doi.org/10.4103/ijo.IJO_812_17 |
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