Occurrence and long-term outcome of tumefactive demyelinating lesions in multiple sclerosis.
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| Title: | Occurrence and long-term outcome of tumefactive demyelinating lesions in multiple sclerosis. |
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| Authors: | Totaro, Rocco, Di Carmine, C., Splendiani, A., Torlone, S., Patriarca, L., Carrocci, C., Sciamanna, S., Marini, C., Carolei, A. |
| Source: | Neurological Sciences. Jul2016, Vol. 37 Issue 7, p1113-1117. 5p. 2 Charts. |
| Subjects: | Multiple sclerosis, Demyelination, Kaplan-Meier estimator, Progression-free survival, Cohort analysis, Disease progression, Prognosis, Functional assessment, Longitudinal method, Magnetic resonance imaging, Survival analysis (Biometry), Proportional hazards models, Disease complications |
| Abstract: | Although tumefactive multiple sclerosis is a well recognized variant of multiple sclerosis, prognostic uncertainty still exists about long term prognosis. The aim of this study was to estimate the occurrence and long term outcome of tumefactive demyelinating lesions (TDLs) in a cohort of multiple sclerosis patients. We reviewed brain MRI of 443 patients referred to our MS clinic. All patients meeting the McDonald criteria for multiple sclerosis and showing at least one TDL were included. Kaplan-Meier estimates of disease-free survival in patient cohort were compared with control group without TDLs using a log-rank test. Seven cases with TDLs were identified (occurrence 1.58 %). Tumefactive demyelinating lesion recurrence was 16.6 %. Cumulative proportion of patients free from clinical relapse and from new T2 lesions was lower in the control group although not reaching statistical significance (30 vs 50 %; P = 0.666 and 21.7 vs 33.3 %; P = 0.761, respectively). Disability progression analysis showed a not significant trend towards lower probability of remaining progression free for TDL patients (50 vs 61 %; P = 0.295). Occurrence of tumefactive demyelinating lesions in our cohort was higher than those reported in other studies. Overall, TDLs were not predictive of poor outcome in terms of disability progression. [ABSTRACT FROM AUTHOR] |
| Copyright of Neurological Sciences is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 116324315 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Occurrence and long-term outcome of tumefactive demyelinating lesions in multiple sclerosis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Totaro%2C+Rocco%22">Totaro, Rocco</searchLink><br /><searchLink fieldCode="AR" term="%22Di+Carmine%2C+C%2E%22">Di Carmine, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Splendiani%2C+A%2E%22">Splendiani, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Torlone%2C+S%2E%22">Torlone, S.</searchLink><br /><searchLink fieldCode="AR" term="%22Patriarca%2C+L%2E%22">Patriarca, L.</searchLink><br /><searchLink fieldCode="AR" term="%22Carrocci%2C+C%2E%22">Carrocci, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Sciamanna%2C+S%2E%22">Sciamanna, S.</searchLink><br /><searchLink fieldCode="AR" term="%22Marini%2C+C%2E%22">Marini, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Carolei%2C+A%2E%22">Carolei, A.</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neurological+Sciences%22">Neurological Sciences</searchLink>. Jul2016, Vol. 37 Issue 7, p1113-1117. 5p. 2 Charts. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Multiple+sclerosis%22">Multiple sclerosis</searchLink><br /><searchLink fieldCode="DE" term="%22Demyelination%22">Demyelination</searchLink><br /><searchLink fieldCode="DE" term="%22Kaplan-Meier+estimator%22">Kaplan-Meier estimator</searchLink><br /><searchLink fieldCode="DE" term="%22Progression-free+survival%22">Progression-free survival</searchLink><br /><searchLink fieldCode="DE" term="%22Cohort+analysis%22">Cohort analysis</searchLink><br /><searchLink fieldCode="DE" term="%22Disease+progression%22">Disease progression</searchLink><br /><searchLink fieldCode="DE" term="%22Prognosis%22">Prognosis</searchLink><br /><searchLink fieldCode="DE" term="%22Functional+assessment%22">Functional assessment</searchLink><br /><searchLink fieldCode="DE" term="%22Longitudinal+method%22">Longitudinal method</searchLink><br /><searchLink fieldCode="DE" term="%22Magnetic+resonance+imaging%22">Magnetic resonance imaging</searchLink><br /><searchLink fieldCode="DE" term="%22Survival+analysis+%28Biometry%29%22">Survival analysis (Biometry)</searchLink><br /><searchLink fieldCode="DE" term="%22Proportional+hazards+models%22">Proportional hazards models</searchLink><br /><searchLink fieldCode="DE" term="%22Disease+complications%22">Disease complications</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Although tumefactive multiple sclerosis is a well recognized variant of multiple sclerosis, prognostic uncertainty still exists about long term prognosis. The aim of this study was to estimate the occurrence and long term outcome of tumefactive demyelinating lesions (TDLs) in a cohort of multiple sclerosis patients. We reviewed brain MRI of 443 patients referred to our MS clinic. All patients meeting the McDonald criteria for multiple sclerosis and showing at least one TDL were included. Kaplan-Meier estimates of disease-free survival in patient cohort were compared with control group without TDLs using a log-rank test. Seven cases with TDLs were identified (occurrence 1.58 %). Tumefactive demyelinating lesion recurrence was 16.6 %. Cumulative proportion of patients free from clinical relapse and from new T2 lesions was lower in the control group although not reaching statistical significance (30 vs 50 %; P = 0.666 and 21.7 vs 33.3 %; P = 0.761, respectively). Disability progression analysis showed a not significant trend towards lower probability of remaining progression free for TDL patients (50 vs 61 %; P = 0.295). Occurrence of tumefactive demyelinating lesions in our cohort was higher than those reported in other studies. Overall, TDLs were not predictive of poor outcome in terms of disability progression. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Neurological Sciences is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s10072-016-2558-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1113 Subjects: – SubjectFull: Multiple sclerosis Type: general – SubjectFull: Demyelination Type: general – SubjectFull: Kaplan-Meier estimator Type: general – SubjectFull: Progression-free survival Type: general – SubjectFull: Cohort analysis Type: general – SubjectFull: Disease progression Type: general – SubjectFull: Prognosis Type: general – SubjectFull: Functional assessment Type: general – SubjectFull: Longitudinal method Type: general – SubjectFull: Magnetic resonance imaging Type: general – SubjectFull: Survival analysis (Biometry) Type: general – SubjectFull: Proportional hazards models Type: general – SubjectFull: Disease complications Type: general Titles: – TitleFull: Occurrence and long-term outcome of tumefactive demyelinating lesions in multiple sclerosis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Totaro, Rocco – PersonEntity: Name: NameFull: Di Carmine, C. – PersonEntity: Name: NameFull: Splendiani, A. – PersonEntity: Name: NameFull: Torlone, S. – PersonEntity: Name: NameFull: Patriarca, L. – PersonEntity: Name: NameFull: Carrocci, C. – PersonEntity: Name: NameFull: Sciamanna, S. – PersonEntity: Name: NameFull: Marini, C. – PersonEntity: Name: NameFull: Carolei, A. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: Jul2016 Type: published Y: 2016 Identifiers: – Type: issn-print Value: 15901874 Numbering: – Type: volume Value: 37 – Type: issue Value: 7 Titles: – TitleFull: Neurological Sciences Type: main |
| ResultId | 1 |