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Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy

Background: Progressive multifocal leukoencephalopathy (PML) is a viral disease characterized by progressive damage or inflammation of the cerebral white matter that can be encountered in patients with multiple sclerosis (MS). There are cases of PML caused by pharmacological agents including nataliz...

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Autores principales: Lo Buono, Viviana, D’Aleo, Giangaetano, Cammaroto, Simona, De Cola, Maria Cristina, Palmese, Francesca, Smorto, Chiara, Marino, Silvia, Venuti, Giuseppe, Sessa, Edoardo, Rifici, Carmela, Corallo, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025511/
https://www.ncbi.nlm.nih.gov/pubmed/35454389
http://dx.doi.org/10.3390/medicina58040551
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author Lo Buono, Viviana
D’Aleo, Giangaetano
Cammaroto, Simona
De Cola, Maria Cristina
Palmese, Francesca
Smorto, Chiara
Marino, Silvia
Venuti, Giuseppe
Sessa, Edoardo
Rifici, Carmela
Corallo, Francesco
author_facet Lo Buono, Viviana
D’Aleo, Giangaetano
Cammaroto, Simona
De Cola, Maria Cristina
Palmese, Francesca
Smorto, Chiara
Marino, Silvia
Venuti, Giuseppe
Sessa, Edoardo
Rifici, Carmela
Corallo, Francesco
author_sort Lo Buono, Viviana
collection PubMed
description Background: Progressive multifocal leukoencephalopathy (PML) is a viral disease characterized by progressive damage or inflammation of the cerebral white matter that can be encountered in patients with multiple sclerosis (MS). There are cases of PML caused by pharmacological agents including natalizumab. Therefore, in patients treated with this drug, early identification of PML allows changes in the treatment plan, reducing the risks of morbidity and mortality. Case presentation: We reported the case of a 57-year-old female diagnosed with relapsing-remitting MS, who presented with PML related to natalizumab. The patient presented with change in behavioral, radiological abnormalities in the left parieto-temporal lobes. We described the longitudinal course of PML, from the diagnosis until the patient’s death, documenting the progressive deterioration of her cognitive functioning, supported by changes on sequential brain scans and neurophysiological data. Conclusion: The neuropsychological impairment documented in this case study expands the range of treatment-related complications associated with natalizumab, and provides evidence that occurrence of “atypical” cognitive deficits in MS may support the early diagnosis of PML.
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spelling pubmed-90255112022-04-23 Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy Lo Buono, Viviana D’Aleo, Giangaetano Cammaroto, Simona De Cola, Maria Cristina Palmese, Francesca Smorto, Chiara Marino, Silvia Venuti, Giuseppe Sessa, Edoardo Rifici, Carmela Corallo, Francesco Medicina (Kaunas) Case Report Background: Progressive multifocal leukoencephalopathy (PML) is a viral disease characterized by progressive damage or inflammation of the cerebral white matter that can be encountered in patients with multiple sclerosis (MS). There are cases of PML caused by pharmacological agents including natalizumab. Therefore, in patients treated with this drug, early identification of PML allows changes in the treatment plan, reducing the risks of morbidity and mortality. Case presentation: We reported the case of a 57-year-old female diagnosed with relapsing-remitting MS, who presented with PML related to natalizumab. The patient presented with change in behavioral, radiological abnormalities in the left parieto-temporal lobes. We described the longitudinal course of PML, from the diagnosis until the patient’s death, documenting the progressive deterioration of her cognitive functioning, supported by changes on sequential brain scans and neurophysiological data. Conclusion: The neuropsychological impairment documented in this case study expands the range of treatment-related complications associated with natalizumab, and provides evidence that occurrence of “atypical” cognitive deficits in MS may support the early diagnosis of PML. MDPI 2022-04-17 /pmc/articles/PMC9025511/ /pubmed/35454389 http://dx.doi.org/10.3390/medicina58040551 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
Lo Buono, Viviana
D’Aleo, Giangaetano
Cammaroto, Simona
De Cola, Maria Cristina
Palmese, Francesca
Smorto, Chiara
Marino, Silvia
Venuti, Giuseppe
Sessa, Edoardo
Rifici, Carmela
Corallo, Francesco
Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy
title Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy
title_full Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy
title_fullStr Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy
title_full_unstemmed Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy
title_short Neuropsychological Disability in the Case of Natalizumab-Related Progressive Multifocal Leukoencephalopathy
title_sort neuropsychological disability in the case of natalizumab-related progressive multifocal leukoencephalopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025511/
https://www.ncbi.nlm.nih.gov/pubmed/35454389
http://dx.doi.org/10.3390/medicina58040551
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