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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...

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Autores principales: Panigrahi, Pradeep Kumar, Minj, Anita, Satapathy, Jasmita
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/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.
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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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