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DC Field | Value | Language |
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dc.contributor.author | Pervin, I. | - |
dc.contributor.author | Ramanathan, S. | - |
dc.contributor.author | Cappelen-Smith, C. | - |
dc.contributor.author | Vucic, S. | - |
dc.contributor.author | Reddel, S. W. | - |
dc.contributor.author | Hardy, T. A. | - |
dc.date.accessioned | 2024-03-11T01:57:24Z | - |
dc.date.available | 2024-03-11T01:57:24Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 22110348 (ISSN) | - |
dc.identifier.uri | https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12577 | - |
dc.description.abstract | Background: Relapsing or recurrent tumefactive demyelination is rare and has not been studied beyond individual case reports. Objective: We examined the clinical course, neuroimaging, cerebrospinal fluid (CSF), treatment and outcomes of patients with recurrent tumefactive demyelinating lesions (TDLs). Methods: We used PubMed to identify reports of recurrent TDLs and included the details of an additional, unpublished patient. Results: We identified 18 cases (11F, 7 M). The median age at onset of the index TDL was 37 years (range 12?72) and most were solitary lesions 72 % (13/18). CSF-restricted oligoclonal bands (OCBs) were detected in 25 % (4/16). Only one of those tested (n = 13) was positive for AQP4-IgG. A moderate-to-marked treatment response (high dose corticosteroid with or without additional plasmapheresis, IVIg or disease modifying therapies) was evident in 89 % of treated patients. Median EDSS at the median follow-up of 36 months (range 6?144) was 2 (range 1?10). Most remained ambulatory (EDSS < 4 in 13/18), but 1 patient died. Conclusion: The median age of patients with relapsing TDLs is similar to that of typical MS, but differences include a lower female:male sex ratio, larger lesions, and a comparative lack of CSF-restricted OCBs. Outcomes vary among this group of patients ranging from minimal disability through to death. � 2023 | - |
dc.publisher | Elsevier B.V. | - |
dc.subject | ADEM Balo concentric sclerosis Demyelinating MOGAD MRI Multiple sclerosis NMOSD Prognosis Pseudotumoral Pseudotumour Therapy Adolescent Adrenal Cortex Hormones Adult Aged Child Demyelinating Diseases Female Humans Magnetic Resonance Imaging Male Middle Aged Neuroimaging Radiography Recurrence Retrospective Studies Young Adult alemtuzumab anticonvulsive agent aquaporin 4 antibody azathioprine beta1a interferon beta1b interferon cladribine cyclophosphamide daclizumab dexamethasone fingolimod glatiramer immunoglobulin methylprednisolone mycophenolate mofetil natalizumab oligoclonal band rituximab corticosteroid Article astrocytoma brain biopsy cerebrospinal fluid analysis clinical article craniotomy cytoreductive surgery death drug megadose drug substitution drug withdrawal Expanded Disability Status Scale fluorescence activated cell sorting follow up human human tissue leukocyte count longitudinally extensive transverse myelitis motor dysfunction myelooptic neuropathy nuclear magnetic resonance imaging nuclear magnetic resonance spectroscopy orchiectomy plasmapheresis protein cerebrospinal fluid level relapse renal cell carcinoma retrospective study seizure seminoma sensory dysfunction sex ratio tumefactive demyelinating lesion tumefactive multiple sclerosis visual field defect demyelinating disease diagnostic imaging recurrent disease | - |
dc.title | Clinical and radiological characteristics and outcomes of patients with recurrent or relapsing tumefactive demyelination | - |
dc.type | Journal Article | - |
dc.contributor.swslhdauthor | Cappelen-Smith, Cecilia | - |
dc.description.affiliates | Multiple sclerosis and Neuroimmunology Clinics, Concord Hospital, University of Sydney, NSW, Australia Translational Neuroimmunology Group, Faculty of medicine and health, University of Sydney, NSW, Australia Brain & Mind Centre, University of Sydney, NSW, Australia Department of Neurology, Liverpool Hospital, Sydney, NSW, Australia | - |
dc.identifier.doi | 10.1016/j.msard.2023.105408 | - |
dc.identifier.department | Liverpool Hospital, Department of Neurology and Neurophysiology | - |
dc.type.studyortrial | Article | - |
dc.identifier.journaltitle | Multiple Sclerosis and Related Disorders | - |
Appears in Collections: | Liverpool Hospital |
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