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Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review

Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in childhood, while multiple sclerosis (MS) is a demyelinating disease of the central nervous system, characterized by remission and exacerbation phases. An association between MS and rheumatologic diseases, in particular rheum...

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Autores principales: Chighizola, Cecilia Beatrice, Ferrito, Matteo, Marelli, Luca, Pontikaki, Irene, Nucci, Paolo, Miserocchi, Elisabetta, Caporali, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405697/
https://www.ncbi.nlm.nih.gov/pubmed/36009588
http://dx.doi.org/10.3390/biomedicines10082041
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author Chighizola, Cecilia Beatrice
Ferrito, Matteo
Marelli, Luca
Pontikaki, Irene
Nucci, Paolo
Miserocchi, Elisabetta
Caporali, Roberto
author_facet Chighizola, Cecilia Beatrice
Ferrito, Matteo
Marelli, Luca
Pontikaki, Irene
Nucci, Paolo
Miserocchi, Elisabetta
Caporali, Roberto
author_sort Chighizola, Cecilia Beatrice
collection PubMed
description Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in childhood, while multiple sclerosis (MS) is a demyelinating disease of the central nervous system, characterized by remission and exacerbation phases. An association between MS and rheumatologic diseases, in particular rheumatoid arthritis, has been described and numerous studies acknowledge anti-TNF-α drugs as MS triggers. Conversely, the association between MS and JIA has been reported merely in five cases in the literature. We describe two cases of adult patients with longstanding JIA and JIA-associated uveitis, who developed MS. The first patient was on methotrexate and adalimumab when she developed dizziness and nausea. Characteristic MRI lesions and oligoclonal bands in cerebrospinal fluid led to MS diagnosis. Adalimumab was discontinued, and she was treated with three pulses of intravenous methylprednisolone. After a few months, rituximab was started. The second patient had been treated with anti-TNF-α and then switched to abatacept. She complained of unilateral arm and facial paraesthesias; brain MRI showed characteristic lesions, and MS was diagnosed. Three pulses of intravenous methylprednisolone were administered; neurological disease remained stable, and abatacept was reintroduced. Further studies are warranted to define if there is an association between JIA and MS, if MS represents JIA comorbidity or if anti-TNF-α underpins MS development.
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spelling pubmed-94056972022-08-26 Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review Chighizola, Cecilia Beatrice Ferrito, Matteo Marelli, Luca Pontikaki, Irene Nucci, Paolo Miserocchi, Elisabetta Caporali, Roberto Biomedicines Case Report Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in childhood, while multiple sclerosis (MS) is a demyelinating disease of the central nervous system, characterized by remission and exacerbation phases. An association between MS and rheumatologic diseases, in particular rheumatoid arthritis, has been described and numerous studies acknowledge anti-TNF-α drugs as MS triggers. Conversely, the association between MS and JIA has been reported merely in five cases in the literature. We describe two cases of adult patients with longstanding JIA and JIA-associated uveitis, who developed MS. The first patient was on methotrexate and adalimumab when she developed dizziness and nausea. Characteristic MRI lesions and oligoclonal bands in cerebrospinal fluid led to MS diagnosis. Adalimumab was discontinued, and she was treated with three pulses of intravenous methylprednisolone. After a few months, rituximab was started. The second patient had been treated with anti-TNF-α and then switched to abatacept. She complained of unilateral arm and facial paraesthesias; brain MRI showed characteristic lesions, and MS was diagnosed. Three pulses of intravenous methylprednisolone were administered; neurological disease remained stable, and abatacept was reintroduced. Further studies are warranted to define if there is an association between JIA and MS, if MS represents JIA comorbidity or if anti-TNF-α underpins MS development. MDPI 2022-08-21 /pmc/articles/PMC9405697/ /pubmed/36009588 http://dx.doi.org/10.3390/biomedicines10082041 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Chighizola, Cecilia Beatrice
Ferrito, Matteo
Marelli, Luca
Pontikaki, Irene
Nucci, Paolo
Miserocchi, Elisabetta
Caporali, Roberto
Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review
title Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review
title_full Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review
title_fullStr Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review
title_full_unstemmed Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review
title_short Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review
title_sort juvenile idiopathic arthritis, uveitis and multiple sclerosis: description of two patients and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405697/
https://www.ncbi.nlm.nih.gov/pubmed/36009588
http://dx.doi.org/10.3390/biomedicines10082041
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