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Rheumatoid Cerebral Vasculitis in a Patient in Remission
Cerebral vasculitis is a very rare extra-articular complication of rheumatoid arthritis (RA) that is often challenging to diagnose. Elevated titers of rheumatoid factor (RF), anti-cyclic citrullinated peptide antibodies (anti-CCP), and antinuclear antibodies (ANA) have been linked with severe compli...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915229/ https://www.ncbi.nlm.nih.gov/pubmed/35283656 http://dx.doi.org/10.1177/11795476221083114 |
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author | El Hasbani, Georges El Ouweini, Hala Dabdoub, Fatema Hourani, Roula Jawad, Ali SM Uthman, Imad |
author_facet | El Hasbani, Georges El Ouweini, Hala Dabdoub, Fatema Hourani, Roula Jawad, Ali SM Uthman, Imad |
author_sort | El Hasbani, Georges |
collection | PubMed |
description | Cerebral vasculitis is a very rare extra-articular complication of rheumatoid arthritis (RA) that is often challenging to diagnose. Elevated titers of rheumatoid factor (RF), anti-cyclic citrullinated peptide antibodies (anti-CCP), and antinuclear antibodies (ANA) have been linked with severe complications. The absence of highly elevated titers of RF, anti-CCP, and ANA can complicate the diagnosis of RA-associated cerebral vasculitis. We report the case of a 59-year-old woman with long-standing arthritis maintained on rituximab and leflunomide who developed sudden headaches and altered level of consciousness. Laboratory work-up revealed normal lymphocyte count and mildly elevated total serum protein and anti-CCP with negative RF and ANA and no evidence for viral or bacterial infections. Cerebrospinal fluid analysis (CSF) showed slightly elevated anti-CCP with normal levels of CXCL-13 and interleukin 6 (IL-6). Brain magnetic resonance imaging (MRI) showed ill-defined lesion of high T2 signal. Using MR angiogram, MR perfusion, and MR spectroscopy, the diagnosis of rheumatoid cerebral vasculitis was confirmed. The patient was treated with intravenous methyl-prednisolone with fast complete improvement. We conclude that adequate immunosuppression in RA might not be able to prevent rare extra-articular manifestations such as rheumatoid cerebral vasculitis. |
format | Online Article Text |
id | pubmed-8915229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-89152292022-03-12 Rheumatoid Cerebral Vasculitis in a Patient in Remission El Hasbani, Georges El Ouweini, Hala Dabdoub, Fatema Hourani, Roula Jawad, Ali SM Uthman, Imad Clin Med Insights Case Rep Case Report Cerebral vasculitis is a very rare extra-articular complication of rheumatoid arthritis (RA) that is often challenging to diagnose. Elevated titers of rheumatoid factor (RF), anti-cyclic citrullinated peptide antibodies (anti-CCP), and antinuclear antibodies (ANA) have been linked with severe complications. The absence of highly elevated titers of RF, anti-CCP, and ANA can complicate the diagnosis of RA-associated cerebral vasculitis. We report the case of a 59-year-old woman with long-standing arthritis maintained on rituximab and leflunomide who developed sudden headaches and altered level of consciousness. Laboratory work-up revealed normal lymphocyte count and mildly elevated total serum protein and anti-CCP with negative RF and ANA and no evidence for viral or bacterial infections. Cerebrospinal fluid analysis (CSF) showed slightly elevated anti-CCP with normal levels of CXCL-13 and interleukin 6 (IL-6). Brain magnetic resonance imaging (MRI) showed ill-defined lesion of high T2 signal. Using MR angiogram, MR perfusion, and MR spectroscopy, the diagnosis of rheumatoid cerebral vasculitis was confirmed. The patient was treated with intravenous methyl-prednisolone with fast complete improvement. We conclude that adequate immunosuppression in RA might not be able to prevent rare extra-articular manifestations such as rheumatoid cerebral vasculitis. SAGE Publications 2022-03-09 /pmc/articles/PMC8915229/ /pubmed/35283656 http://dx.doi.org/10.1177/11795476221083114 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report El Hasbani, Georges El Ouweini, Hala Dabdoub, Fatema Hourani, Roula Jawad, Ali SM Uthman, Imad Rheumatoid Cerebral Vasculitis in a Patient in Remission |
title | Rheumatoid Cerebral Vasculitis in a Patient in Remission |
title_full | Rheumatoid Cerebral Vasculitis in a Patient in Remission |
title_fullStr | Rheumatoid Cerebral Vasculitis in a Patient in Remission |
title_full_unstemmed | Rheumatoid Cerebral Vasculitis in a Patient in Remission |
title_short | Rheumatoid Cerebral Vasculitis in a Patient in Remission |
title_sort | rheumatoid cerebral vasculitis in a patient in remission |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915229/ https://www.ncbi.nlm.nih.gov/pubmed/35283656 http://dx.doi.org/10.1177/11795476221083114 |
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