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A case of neurosarcoidosis presenting with multiple cranial neuropathies
PURPOSE: We report a case of neurosarcoidosis that presented simultaneously with oculomotor nerve palsy, contralateral abducens nerve palsy, and paresthesia of both lower limbs. OBSERVATIONS: A 69-year-old Japanese woman who suffered from repeated diplopia and lower-limb paresthesia was referred to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330492/ https://www.ncbi.nlm.nih.gov/pubmed/32637734 http://dx.doi.org/10.1016/j.ajoc.2020.100796 |
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author | Mori, Sotaro Kurimoto, Takuji Ueda, Kaori Sakamoto, Mari Chihara, Norio Satake, Wataru Yamada-Nakanishi, Yuko Nakamura, Makoto |
author_facet | Mori, Sotaro Kurimoto, Takuji Ueda, Kaori Sakamoto, Mari Chihara, Norio Satake, Wataru Yamada-Nakanishi, Yuko Nakamura, Makoto |
author_sort | Mori, Sotaro |
collection | PubMed |
description | PURPOSE: We report a case of neurosarcoidosis that presented simultaneously with oculomotor nerve palsy, contralateral abducens nerve palsy, and paresthesia of both lower limbs. OBSERVATIONS: A 69-year-old Japanese woman who suffered from repeated diplopia and lower-limb paresthesia was referred to our hospital. Ophthalmic findings included oculomotor nerve and contralateral abducens nerve palsies. No remarkable abnormalities were detected via enhanced brain magnetic resonance imaging (MRI), chest X-ray, and cerebrospinal fluid analysis. Chest computed tomography (CT) was performed to exclude neoplastic lesions; this revealed right hilar lymphadenopathy, and positron emission tomography MRI showed strong 18-F fluorodeoxyglucose uptake in the hilar lymph node. Biopsy of the lymph node showed non-caseating epithelioid granulomatous tissue, leading to a diagnosis of probable neurosarcoidosis. After the initiation of oral prednisolone treatment, the patient experienced complete remission without any recurrence. CONCLUSIONS AND IMPORTANCE: When examining a patient presenting with multiple cranial neuropathies of unknown cause, neurosarcoidosis should be considered as a differential diagnosis and chest CT should be performed even when the chest X-ray and angiotensin-converting enzyme appears normal. |
format | Online Article Text |
id | pubmed-7330492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-73304922020-07-06 A case of neurosarcoidosis presenting with multiple cranial neuropathies Mori, Sotaro Kurimoto, Takuji Ueda, Kaori Sakamoto, Mari Chihara, Norio Satake, Wataru Yamada-Nakanishi, Yuko Nakamura, Makoto Am J Ophthalmol Case Rep Case Report PURPOSE: We report a case of neurosarcoidosis that presented simultaneously with oculomotor nerve palsy, contralateral abducens nerve palsy, and paresthesia of both lower limbs. OBSERVATIONS: A 69-year-old Japanese woman who suffered from repeated diplopia and lower-limb paresthesia was referred to our hospital. Ophthalmic findings included oculomotor nerve and contralateral abducens nerve palsies. No remarkable abnormalities were detected via enhanced brain magnetic resonance imaging (MRI), chest X-ray, and cerebrospinal fluid analysis. Chest computed tomography (CT) was performed to exclude neoplastic lesions; this revealed right hilar lymphadenopathy, and positron emission tomography MRI showed strong 18-F fluorodeoxyglucose uptake in the hilar lymph node. Biopsy of the lymph node showed non-caseating epithelioid granulomatous tissue, leading to a diagnosis of probable neurosarcoidosis. After the initiation of oral prednisolone treatment, the patient experienced complete remission without any recurrence. CONCLUSIONS AND IMPORTANCE: When examining a patient presenting with multiple cranial neuropathies of unknown cause, neurosarcoidosis should be considered as a differential diagnosis and chest CT should be performed even when the chest X-ray and angiotensin-converting enzyme appears normal. Elsevier 2020-06-27 /pmc/articles/PMC7330492/ /pubmed/32637734 http://dx.doi.org/10.1016/j.ajoc.2020.100796 Text en © 2020 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Mori, Sotaro Kurimoto, Takuji Ueda, Kaori Sakamoto, Mari Chihara, Norio Satake, Wataru Yamada-Nakanishi, Yuko Nakamura, Makoto A case of neurosarcoidosis presenting with multiple cranial neuropathies |
title | A case of neurosarcoidosis presenting with multiple cranial neuropathies |
title_full | A case of neurosarcoidosis presenting with multiple cranial neuropathies |
title_fullStr | A case of neurosarcoidosis presenting with multiple cranial neuropathies |
title_full_unstemmed | A case of neurosarcoidosis presenting with multiple cranial neuropathies |
title_short | A case of neurosarcoidosis presenting with multiple cranial neuropathies |
title_sort | case of neurosarcoidosis presenting with multiple cranial neuropathies |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330492/ https://www.ncbi.nlm.nih.gov/pubmed/32637734 http://dx.doi.org/10.1016/j.ajoc.2020.100796 |
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