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Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy

PURPOSE: To report a case of non-paraneoplastic autoimmune retinopathy (npAIR) treated with intravenous immunoglobulin (IVIG). CASE REPORT: A 12-year-old boy presented with progressive visual field loss, nyctalopia, and flashing for three months. He had suffered from common cold two weeks before the...

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Autores principales: Fekri, Sahba, Soheilian, Masoud, Rahimi-Ardabili, Babak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PUBLISHED BY KNOWLEDGE E 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151517/
https://www.ncbi.nlm.nih.gov/pubmed/32308960
http://dx.doi.org/10.18502/jovr.v15i2.6743
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author Fekri, Sahba
Soheilian, Masoud
Rahimi-Ardabili, Babak
author_facet Fekri, Sahba
Soheilian, Masoud
Rahimi-Ardabili, Babak
author_sort Fekri, Sahba
collection PubMed
description PURPOSE: To report a case of non-paraneoplastic autoimmune retinopathy (npAIR) treated with intravenous immunoglobulin (IVIG). CASE REPORT: A 12-year-old boy presented with progressive visual field loss, nyctalopia, and flashing for three months. He had suffered from common cold two weeks before the onset of these symptoms. On the basis of clinical history and paraclinical findings, he was diagnosed with npAIR, and IVIG without immunosuppressive therapy was started. During the one-year follow-up period after the first course of IVIG, flashing disappeared completely. Visual acuity remained 10/10, but nyctalopia did not improve. Multimodal imaging showed no disease progression. CONCLUSION: Although established retinal degenerative changes seem irreversible in npAIR, IVIG may be a suitable choice to control the disease progression.
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spelling pubmed-71515172020-04-17 Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy Fekri, Sahba Soheilian, Masoud Rahimi-Ardabili, Babak J Ophthalmic Vis Res Case Report PURPOSE: To report a case of non-paraneoplastic autoimmune retinopathy (npAIR) treated with intravenous immunoglobulin (IVIG). CASE REPORT: A 12-year-old boy presented with progressive visual field loss, nyctalopia, and flashing for three months. He had suffered from common cold two weeks before the onset of these symptoms. On the basis of clinical history and paraclinical findings, he was diagnosed with npAIR, and IVIG without immunosuppressive therapy was started. During the one-year follow-up period after the first course of IVIG, flashing disappeared completely. Visual acuity remained 10/10, but nyctalopia did not improve. Multimodal imaging showed no disease progression. CONCLUSION: Although established retinal degenerative changes seem irreversible in npAIR, IVIG may be a suitable choice to control the disease progression. PUBLISHED BY KNOWLEDGE E 2020-04-06 /pmc/articles/PMC7151517/ /pubmed/32308960 http://dx.doi.org/10.18502/jovr.v15i2.6743 Text en Copyright © 2020 Fekri et al. https://creativecommons.org/licenses/by/4.0/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. which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Case Report
Fekri, Sahba
Soheilian, Masoud
Rahimi-Ardabili, Babak
Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy
title Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy
title_full Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy
title_fullStr Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy
title_full_unstemmed Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy
title_short Intravenous Immunoglobulin for Management of Non-paraneoplastic Autoimmune Retinopathy
title_sort intravenous immunoglobulin for management of non-paraneoplastic autoimmune retinopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151517/
https://www.ncbi.nlm.nih.gov/pubmed/32308960
http://dx.doi.org/10.18502/jovr.v15i2.6743
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