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Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient
BACKGROUND: Neurosarcoidosis is a rare systemic disorder that can affect the eye and other organs, including the central nervous system. Neurosarcoidosis infiltrating the optic nerve presenting as central retinal vein occlusion combined with artery ischaemia has not been reported in the literature p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457306/ https://www.ncbi.nlm.nih.gov/pubmed/32854651 http://dx.doi.org/10.1186/s12886-020-01624-5 |
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author | Feng, Chaoyi Chen, Qian Liu, Wei Bi, Yingwen Qian, Jiang Wang, Min Sun, Xinghuai Tian, Guohong |
author_facet | Feng, Chaoyi Chen, Qian Liu, Wei Bi, Yingwen Qian, Jiang Wang, Min Sun, Xinghuai Tian, Guohong |
author_sort | Feng, Chaoyi |
collection | PubMed |
description | BACKGROUND: Neurosarcoidosis is a rare systemic disorder that can affect the eye and other organs, including the central nervous system. Neurosarcoidosis infiltrating the optic nerve presenting as central retinal vein occlusion combined with artery ischaemia has not been reported in the literature previously. We describe a Chinese patient presenting with acute monocular vision loss, in whom an optic nerve biopsy confirmed the diagnosis of neurosarcoidosis. CASE PRESENTATION: A 47-year-old woman complained of acute decreased vision in her left eye over the course of 1 month. She reported that her vision deteriorated quickly within first 3 days of consulting an ophthalmologist at a local hospital. She was diagnosed with central retinal vein occlusion after funduscopic examination and fundus fluorescein angiography, and the vision in her left eye further deteriorated to no light perception. An orbital magnetic resonance imaging showed an abnormal T1-weighted image of the optic nerve after contrast enhancement. She was referred to a neuro-ophthalmologist for further evaluation. After routine blood tests ruled out infectious and metastatic diseases, she was prescribed 500 mg/d methylprednisolone for 5 days, but her vision did not improve. As she could still not perceive light, an optic nerve biopsy was performed, and the histopathology revealed non-necrotising granuloma that was consistent with neurosarcoidosis. CONCLUSIONS: Isolated optic nerve infiltration by neurosarcoidosis without the involvement of the central nervous system or other systemic organs is challenging to diagnose. Biopsy of the optic nerve sheath is crucial for the final diagnosis of neurosarcoidosis. Therefore, a comprehensive ophthalmologic and systemic examination and work-up for inflammation of the eye, chest, and central nervous system should be conducted for atypical cases. |
format | Online Article Text |
id | pubmed-7457306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74573062020-08-31 Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient Feng, Chaoyi Chen, Qian Liu, Wei Bi, Yingwen Qian, Jiang Wang, Min Sun, Xinghuai Tian, Guohong BMC Ophthalmol Case Report BACKGROUND: Neurosarcoidosis is a rare systemic disorder that can affect the eye and other organs, including the central nervous system. Neurosarcoidosis infiltrating the optic nerve presenting as central retinal vein occlusion combined with artery ischaemia has not been reported in the literature previously. We describe a Chinese patient presenting with acute monocular vision loss, in whom an optic nerve biopsy confirmed the diagnosis of neurosarcoidosis. CASE PRESENTATION: A 47-year-old woman complained of acute decreased vision in her left eye over the course of 1 month. She reported that her vision deteriorated quickly within first 3 days of consulting an ophthalmologist at a local hospital. She was diagnosed with central retinal vein occlusion after funduscopic examination and fundus fluorescein angiography, and the vision in her left eye further deteriorated to no light perception. An orbital magnetic resonance imaging showed an abnormal T1-weighted image of the optic nerve after contrast enhancement. She was referred to a neuro-ophthalmologist for further evaluation. After routine blood tests ruled out infectious and metastatic diseases, she was prescribed 500 mg/d methylprednisolone for 5 days, but her vision did not improve. As she could still not perceive light, an optic nerve biopsy was performed, and the histopathology revealed non-necrotising granuloma that was consistent with neurosarcoidosis. CONCLUSIONS: Isolated optic nerve infiltration by neurosarcoidosis without the involvement of the central nervous system or other systemic organs is challenging to diagnose. Biopsy of the optic nerve sheath is crucial for the final diagnosis of neurosarcoidosis. Therefore, a comprehensive ophthalmologic and systemic examination and work-up for inflammation of the eye, chest, and central nervous system should be conducted for atypical cases. BioMed Central 2020-08-27 /pmc/articles/PMC7457306/ /pubmed/32854651 http://dx.doi.org/10.1186/s12886-020-01624-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Feng, Chaoyi Chen, Qian Liu, Wei Bi, Yingwen Qian, Jiang Wang, Min Sun, Xinghuai Tian, Guohong Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient |
title | Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient |
title_full | Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient |
title_fullStr | Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient |
title_full_unstemmed | Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient |
title_short | Neurosarcoidosis presenting as CRVO combined CRAO: a biopsy-proven case report of a Chinese patient |
title_sort | neurosarcoidosis presenting as crvo combined crao: a biopsy-proven case report of a chinese patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457306/ https://www.ncbi.nlm.nih.gov/pubmed/32854651 http://dx.doi.org/10.1186/s12886-020-01624-5 |
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