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Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report

In this study, we present a case of bilateral optic neuropathy and macular ischemia in the right eye associated with neurosarcoidosis. A 26-year-old woman presented to our clinic with complaints of bilateral blurred vision. Bilateral granulomatous anterior uveitis, vitritis, optic neuropathy, and ma...

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Autores principales: Tanyıldız, Burak, Doğan, Gizem, Zorlutuna Kaymak, Nilüfer, Tezcan, Mehmet Engin, Kılıç, Ahmet Kasım, Şener Cömert, Sevda, Karatay Arsan, Aysu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126102/
https://www.ncbi.nlm.nih.gov/pubmed/30202617
http://dx.doi.org/10.4274/tjo.49799
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author Tanyıldız, Burak
Doğan, Gizem
Zorlutuna Kaymak, Nilüfer
Tezcan, Mehmet Engin
Kılıç, Ahmet Kasım
Şener Cömert, Sevda
Karatay Arsan, Aysu
author_facet Tanyıldız, Burak
Doğan, Gizem
Zorlutuna Kaymak, Nilüfer
Tezcan, Mehmet Engin
Kılıç, Ahmet Kasım
Şener Cömert, Sevda
Karatay Arsan, Aysu
author_sort Tanyıldız, Burak
collection PubMed
description In this study, we present a case of bilateral optic neuropathy and macular ischemia in the right eye associated with neurosarcoidosis. A 26-year-old woman presented to our clinic with complaints of bilateral blurred vision. Bilateral granulomatous anterior uveitis, vitritis, optic neuropathy, and macular ischemia were detected in the right eye in slit-lamp examination. She also reported complaints of fever, weakness, sweating, arthralgia, and headache for 2 months. She was referred to the pulmonary diseases unit of our hospital due to hilar lymphadenopathy seen in her chest x-ray, and biopsies were taken for diagnostic purposes. Histological analysis of the mediastinal lymph node biopsies revealed chronic, non-caseating, granulomatous inflammation. Furthermore, the patient was referred to a neurologist due to concomitant complaint of intense headaches. She was diagnosed with neurosarcoidosis supported by findings on cranial magnetic resonance imaging and lumbar puncture. She received a 3-day course of high-dose (1 g/day) intravenous steroid treatment (methylprednisolone) followed by a tapering dose of oral prednisone. The patient began receiving oral methotrexate 15 mg/week as a steroid-sparing agent. Significant improvement in neurological and ophthalmological symptoms occurred in the first week of treatment. In this case report, we emphasized that neurosarcoidosis should be included in the differential diagnosis of patients with both bilateral optic neuropathy and macular ischemia. Furthermore, early diagnosis and timely treatment of neurosarcoidosis are important for favorable visual outcomes.
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spelling pubmed-61261022018-09-10 Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report Tanyıldız, Burak Doğan, Gizem Zorlutuna Kaymak, Nilüfer Tezcan, Mehmet Engin Kılıç, Ahmet Kasım Şener Cömert, Sevda Karatay Arsan, Aysu Turk J Ophthalmol Case Report In this study, we present a case of bilateral optic neuropathy and macular ischemia in the right eye associated with neurosarcoidosis. A 26-year-old woman presented to our clinic with complaints of bilateral blurred vision. Bilateral granulomatous anterior uveitis, vitritis, optic neuropathy, and macular ischemia were detected in the right eye in slit-lamp examination. She also reported complaints of fever, weakness, sweating, arthralgia, and headache for 2 months. She was referred to the pulmonary diseases unit of our hospital due to hilar lymphadenopathy seen in her chest x-ray, and biopsies were taken for diagnostic purposes. Histological analysis of the mediastinal lymph node biopsies revealed chronic, non-caseating, granulomatous inflammation. Furthermore, the patient was referred to a neurologist due to concomitant complaint of intense headaches. She was diagnosed with neurosarcoidosis supported by findings on cranial magnetic resonance imaging and lumbar puncture. She received a 3-day course of high-dose (1 g/day) intravenous steroid treatment (methylprednisolone) followed by a tapering dose of oral prednisone. The patient began receiving oral methotrexate 15 mg/week as a steroid-sparing agent. Significant improvement in neurological and ophthalmological symptoms occurred in the first week of treatment. In this case report, we emphasized that neurosarcoidosis should be included in the differential diagnosis of patients with both bilateral optic neuropathy and macular ischemia. Furthermore, early diagnosis and timely treatment of neurosarcoidosis are important for favorable visual outcomes. Galenos Publishing 2018-08 2018-09-04 /pmc/articles/PMC6126102/ /pubmed/30202617 http://dx.doi.org/10.4274/tjo.49799 Text en © 2018 by Turkish Ophthalmological Association Turkish Journal of Ophthalmology, published by Galenos Publishing House. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tanyıldız, Burak
Doğan, Gizem
Zorlutuna Kaymak, Nilüfer
Tezcan, Mehmet Engin
Kılıç, Ahmet Kasım
Şener Cömert, Sevda
Karatay Arsan, Aysu
Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report
title Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report
title_full Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report
title_fullStr Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report
title_full_unstemmed Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report
title_short Optic Neuropathy and Macular Ischemia Associated with Neurosarcoidosis: A Case Report
title_sort optic neuropathy and macular ischemia associated with neurosarcoidosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126102/
https://www.ncbi.nlm.nih.gov/pubmed/30202617
http://dx.doi.org/10.4274/tjo.49799
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