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Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis
BACKGROUND AND PURPOSE: Multiple Sclerosis (MS) has been proposed as a possible differential diagnosis with Fabry Disease (FD). We evaluated the incidence of infratentorial lesions in FD patients, investigating whether their presence could help in differentiating these two conditions. We explored th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236241/ https://www.ncbi.nlm.nih.gov/pubmed/30277321 http://dx.doi.org/10.1002/brb3.1121 |
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author | Ugga, Lorenzo Cocozza, Sirio Pontillo, Giuseppe Russo, Camilla Brescia Morra, Vincenzo Lanzillo, Roberta Riccio, Eleonora Pisani, Antonio Brunetti, Arturo |
author_facet | Ugga, Lorenzo Cocozza, Sirio Pontillo, Giuseppe Russo, Camilla Brescia Morra, Vincenzo Lanzillo, Roberta Riccio, Eleonora Pisani, Antonio Brunetti, Arturo |
author_sort | Ugga, Lorenzo |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Multiple Sclerosis (MS) has been proposed as a possible differential diagnosis with Fabry Disease (FD). We evaluated the incidence of infratentorial lesions in FD patients, investigating whether their presence could help in differentiating these two conditions. We explored the diagnostic accuracy of this sign alone and in combination to the involvement of corpus callosum (CC). METHODS: White Matter lesions were retrospectively evaluated on FLAIR images available from 136 MS and 144 FD patients. Infratentorial involvement was assessed considering the whole cerebellum, and the part of the brainstem included between the occipital foramen and the upper edge of the red nucleus. Furthermore, the presence of callosal lesions was also recorded, evaluating the portion of CC included between the two external walls of the lateral ventricles. RESULTS: Infratentorial involvement was detectable in 119/136 (87.5%) MS patients, while it was present in only 17/144 (11.8%) FD patients. When the diagnostic performance of a positive infratentorial involvement was evaluated in combination with the presence of CC lesions, a specificity of 97%, with a positive predictive value of 96% was reached. CONCLUSIONS: We concluded that the absence of infratentorial lesions, especially when combined to the evaluation of other typical imaging features, can help in the differential diagnosis between MS and FD. |
format | Online Article Text |
id | pubmed-6236241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62362412018-11-20 Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis Ugga, Lorenzo Cocozza, Sirio Pontillo, Giuseppe Russo, Camilla Brescia Morra, Vincenzo Lanzillo, Roberta Riccio, Eleonora Pisani, Antonio Brunetti, Arturo Brain Behav Original Research BACKGROUND AND PURPOSE: Multiple Sclerosis (MS) has been proposed as a possible differential diagnosis with Fabry Disease (FD). We evaluated the incidence of infratentorial lesions in FD patients, investigating whether their presence could help in differentiating these two conditions. We explored the diagnostic accuracy of this sign alone and in combination to the involvement of corpus callosum (CC). METHODS: White Matter lesions were retrospectively evaluated on FLAIR images available from 136 MS and 144 FD patients. Infratentorial involvement was assessed considering the whole cerebellum, and the part of the brainstem included between the occipital foramen and the upper edge of the red nucleus. Furthermore, the presence of callosal lesions was also recorded, evaluating the portion of CC included between the two external walls of the lateral ventricles. RESULTS: Infratentorial involvement was detectable in 119/136 (87.5%) MS patients, while it was present in only 17/144 (11.8%) FD patients. When the diagnostic performance of a positive infratentorial involvement was evaluated in combination with the presence of CC lesions, a specificity of 97%, with a positive predictive value of 96% was reached. CONCLUSIONS: We concluded that the absence of infratentorial lesions, especially when combined to the evaluation of other typical imaging features, can help in the differential diagnosis between MS and FD. John Wiley and Sons Inc. 2018-10-02 /pmc/articles/PMC6236241/ /pubmed/30277321 http://dx.doi.org/10.1002/brb3.1121 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Ugga, Lorenzo Cocozza, Sirio Pontillo, Giuseppe Russo, Camilla Brescia Morra, Vincenzo Lanzillo, Roberta Riccio, Eleonora Pisani, Antonio Brunetti, Arturo Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis |
title | Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis |
title_full | Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis |
title_fullStr | Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis |
title_full_unstemmed | Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis |
title_short | Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis |
title_sort | absence of infratentorial lesions in fabry disease contributes to differential diagnosis with multiple sclerosis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236241/ https://www.ncbi.nlm.nih.gov/pubmed/30277321 http://dx.doi.org/10.1002/brb3.1121 |
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