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Isolated neurosarcoidosis mimicking multiple sclerosis

Patients with isolated neurosarcoidosis (NS) can present with neurological symptoms that mimic other neurologic conditions, such as multiple sclerosis (MS). In this article, we present a case of 25-year-old man with a transverse myelitis. Magnetic resonance imaging (MRI) of the brain and spine showe...

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Autor principal: Malik, Yaser M. Al
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015592/
https://www.ncbi.nlm.nih.gov/pubmed/33459292
http://dx.doi.org/10.17712/nsj.2020.5.20200090
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author Malik, Yaser M. Al
author_facet Malik, Yaser M. Al
author_sort Malik, Yaser M. Al
collection PubMed
description Patients with isolated neurosarcoidosis (NS) can present with neurological symptoms that mimic other neurologic conditions, such as multiple sclerosis (MS). In this article, we present a case of 25-year-old man with a transverse myelitis. Magnetic resonance imaging (MRI) of the brain and spine showed several, periventricular, infratentorial, and spinal cord white matter lesions. He was diagnosed with MS and was started on fingolimod, which did not result in any improvement. Follow-up brain and spine MRI showed a longitudinally extensive lesion with leptomeningeal enhancement. Leptomeningeal and cerebellar biopsy showed non-necrotizing granulomas consistent with neurosarcoidosis. Fingolimod was discontinued. The patient was treated with oral prednisone and infliximab, which ceased the progression of the disease and allowed for slow improvement. Incorrectly diagnosing NS with MS or vice-versa, not only deprives patients of beneficial therapy, but also potentially exposes them to therapies that may be harmful.
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spelling pubmed-80155922021-08-13 Isolated neurosarcoidosis mimicking multiple sclerosis Malik, Yaser M. Al Neurosciences (Riyadh) Case Report Patients with isolated neurosarcoidosis (NS) can present with neurological symptoms that mimic other neurologic conditions, such as multiple sclerosis (MS). In this article, we present a case of 25-year-old man with a transverse myelitis. Magnetic resonance imaging (MRI) of the brain and spine showed several, periventricular, infratentorial, and spinal cord white matter lesions. He was diagnosed with MS and was started on fingolimod, which did not result in any improvement. Follow-up brain and spine MRI showed a longitudinally extensive lesion with leptomeningeal enhancement. Leptomeningeal and cerebellar biopsy showed non-necrotizing granulomas consistent with neurosarcoidosis. Fingolimod was discontinued. The patient was treated with oral prednisone and infliximab, which ceased the progression of the disease and allowed for slow improvement. Incorrectly diagnosing NS with MS or vice-versa, not only deprives patients of beneficial therapy, but also potentially exposes them to therapies that may be harmful. Riyadh : Armed Forces Hospital 2020-10 /pmc/articles/PMC8015592/ /pubmed/33459292 http://dx.doi.org/10.17712/nsj.2020.5.20200090 Text en Copyright: © Neurosciences https://creativecommons.org/licenses/by-nc-sa/3.0/Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.
spellingShingle Case Report
Malik, Yaser M. Al
Isolated neurosarcoidosis mimicking multiple sclerosis
title Isolated neurosarcoidosis mimicking multiple sclerosis
title_full Isolated neurosarcoidosis mimicking multiple sclerosis
title_fullStr Isolated neurosarcoidosis mimicking multiple sclerosis
title_full_unstemmed Isolated neurosarcoidosis mimicking multiple sclerosis
title_short Isolated neurosarcoidosis mimicking multiple sclerosis
title_sort isolated neurosarcoidosis mimicking multiple sclerosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015592/
https://www.ncbi.nlm.nih.gov/pubmed/33459292
http://dx.doi.org/10.17712/nsj.2020.5.20200090
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