Neurosarcoidosis in an adult man with a family history of MS: A case report

KEY CLINICAL MESSAGE: According to this report, a biopsy revealed a diagnosis of neurosarcoidosis in a patient with a history of MS. The development of the disease can be slowed down by early diagnosis and appropriate treatment. ABSTRACT: Neurosarcoidosis is a rare type of sarcoidosis that affects t...

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Autores principales: Mirmosayyeb, Omid, Mohammadzamani, Mahtab, Bagherieh, Sara, Ghaffary, Elham Moases, Azimi, Elham Sadat, Shaygannejad, Aysa, Shaygannejad, Vahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288071/
https://www.ncbi.nlm.nih.gov/pubmed/37361664
http://dx.doi.org/10.1002/ccr3.7605
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author Mirmosayyeb, Omid
Mohammadzamani, Mahtab
Bagherieh, Sara
Ghaffary, Elham Moases
Azimi, Elham Sadat
Shaygannejad, Aysa
Shaygannejad, Vahid
author_facet Mirmosayyeb, Omid
Mohammadzamani, Mahtab
Bagherieh, Sara
Ghaffary, Elham Moases
Azimi, Elham Sadat
Shaygannejad, Aysa
Shaygannejad, Vahid
author_sort Mirmosayyeb, Omid
collection PubMed
description KEY CLINICAL MESSAGE: According to this report, a biopsy revealed a diagnosis of neurosarcoidosis in a patient with a history of MS. The development of the disease can be slowed down by early diagnosis and appropriate treatment. ABSTRACT: Neurosarcoidosis is a rare type of sarcoidosis that affects the central nervous system (CNS). Herein, we present a case of neurosarcoidosis with a history of multiple sclerosis (MS). Based on the pathological findings of the biopsy, a diagnosis of neurosarcoidosis was established. The administration of appropriate treatment at an early stage can assist in decelerating its progression.
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spelling pubmed-102880712023-06-24 Neurosarcoidosis in an adult man with a family history of MS: A case report Mirmosayyeb, Omid Mohammadzamani, Mahtab Bagherieh, Sara Ghaffary, Elham Moases Azimi, Elham Sadat Shaygannejad, Aysa Shaygannejad, Vahid Clin Case Rep Case Report KEY CLINICAL MESSAGE: According to this report, a biopsy revealed a diagnosis of neurosarcoidosis in a patient with a history of MS. The development of the disease can be slowed down by early diagnosis and appropriate treatment. ABSTRACT: Neurosarcoidosis is a rare type of sarcoidosis that affects the central nervous system (CNS). Herein, we present a case of neurosarcoidosis with a history of multiple sclerosis (MS). Based on the pathological findings of the biopsy, a diagnosis of neurosarcoidosis was established. The administration of appropriate treatment at an early stage can assist in decelerating its progression. John Wiley and Sons Inc. 2023-06-22 /pmc/articles/PMC10288071/ /pubmed/37361664 http://dx.doi.org/10.1002/ccr3.7605 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Mirmosayyeb, Omid
Mohammadzamani, Mahtab
Bagherieh, Sara
Ghaffary, Elham Moases
Azimi, Elham Sadat
Shaygannejad, Aysa
Shaygannejad, Vahid
Neurosarcoidosis in an adult man with a family history of MS: A case report
title Neurosarcoidosis in an adult man with a family history of MS: A case report
title_full Neurosarcoidosis in an adult man with a family history of MS: A case report
title_fullStr Neurosarcoidosis in an adult man with a family history of MS: A case report
title_full_unstemmed Neurosarcoidosis in an adult man with a family history of MS: A case report
title_short Neurosarcoidosis in an adult man with a family history of MS: A case report
title_sort neurosarcoidosis in an adult man with a family history of ms: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288071/
https://www.ncbi.nlm.nih.gov/pubmed/37361664
http://dx.doi.org/10.1002/ccr3.7605
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