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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...

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Autores principales: Mori, Sotaro, Kurimoto, Takuji, Ueda, Kaori, Sakamoto, Mari, Chihara, Norio, Satake, Wataru, Yamada-Nakanishi, Yuko, Nakamura, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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.
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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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