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Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis

Multiple sclerosis is a chronic, debilitating disease. Almost one in ten patients with MS has a history of disease onset during childhood. Although numerous therapeutic options exist for adult MS, the available treatments for pediatric patients are still limited. One of the emerging therapies is rit...

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Autores principales: Vartzelis, George, Maritsi, Despoina, Nikolaidou, Maria, Garoufi, Anastasia, Kilidireas, Constantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679848/
https://www.ncbi.nlm.nih.gov/pubmed/31428499
http://dx.doi.org/10.1155/2019/8731613
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author Vartzelis, George
Maritsi, Despoina
Nikolaidou, Maria
Garoufi, Anastasia
Kilidireas, Constantinos
author_facet Vartzelis, George
Maritsi, Despoina
Nikolaidou, Maria
Garoufi, Anastasia
Kilidireas, Constantinos
author_sort Vartzelis, George
collection PubMed
description Multiple sclerosis is a chronic, debilitating disease. Almost one in ten patients with MS has a history of disease onset during childhood. Although numerous therapeutic options exist for adult MS, the available treatments for pediatric patients are still limited. One of the emerging therapies is rituximab, a monoclonal anti-CD20 chimeric antibody that can deplete the CD20+ lymphocyte populations. A 12-year-old boy presented with ataxia, paresthesias, and headache while his brain MRI showed numerous T2 contrast-enhancing lesions. Gamma globulin, steroids, and cyclophosphamide failed to intercept his disease, and he progressed to a rapid clinical and radiological deterioration. Treatment with rituximab reversed the disease course in a dramatic fashion, leading to complete remission.
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spelling pubmed-66798482019-08-19 Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis Vartzelis, George Maritsi, Despoina Nikolaidou, Maria Garoufi, Anastasia Kilidireas, Constantinos Case Rep Pediatr Case Report Multiple sclerosis is a chronic, debilitating disease. Almost one in ten patients with MS has a history of disease onset during childhood. Although numerous therapeutic options exist for adult MS, the available treatments for pediatric patients are still limited. One of the emerging therapies is rituximab, a monoclonal anti-CD20 chimeric antibody that can deplete the CD20+ lymphocyte populations. A 12-year-old boy presented with ataxia, paresthesias, and headache while his brain MRI showed numerous T2 contrast-enhancing lesions. Gamma globulin, steroids, and cyclophosphamide failed to intercept his disease, and he progressed to a rapid clinical and radiological deterioration. Treatment with rituximab reversed the disease course in a dramatic fashion, leading to complete remission. Hindawi 2019-07-21 /pmc/articles/PMC6679848/ /pubmed/31428499 http://dx.doi.org/10.1155/2019/8731613 Text en Copyright © 2019 George Vartzelis et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Vartzelis, George
Maritsi, Despoina
Nikolaidou, Maria
Garoufi, Anastasia
Kilidireas, Constantinos
Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis
title Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis
title_full Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis
title_fullStr Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis
title_full_unstemmed Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis
title_short Rituximab as Rescue Therapy for Aggressive Pediatric Multiple Sclerosis
title_sort rituximab as rescue therapy for aggressive pediatric multiple sclerosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679848/
https://www.ncbi.nlm.nih.gov/pubmed/31428499
http://dx.doi.org/10.1155/2019/8731613
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