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Tenembaum, Sílvia

https://orcid.org/0000-0001-6544-4356

Mayo Clinic

Garrahan Hospital

Citations 11

Differential Diagnosis of Suspected Multiple Sclerosis in Pediatric and Late-Onset Populations
Hua, Le H. , Solomon, Andrew , Tenembaum, Sílvia , Rostásy, Kevin , Newsome, Scott D. , Marrie, Ruth Ann , Magyari, Melinda , Kantarci, Orhun H. , Cohen, Jeffrey A., Bove, Riley , Banwell, Brenda , Magyari, Melinda , Scalfari, Antonio , Rovira, Àlex , Hemmer, Bernhard , Hemingway, Cheryl , Harnegie, Mary Pat , Graves, Jennifer , Corboy, John R. , Waubant, Emmanuelle L.

JAMA Neurology | September 16, 2024 | Volume: 81 | Issue: 11 | Pages: 1210

10.1001/jamaneurol.2024.3062 Get It

Importance While the typical onset of multiple sclerosis (MS) occurs in early adulthood, 2% to 10% of cases initially present prior to age 18 years, and approximately 5% after age 50 years. Guidance on approaches to differential diagnosis in suspected MS specific to these 2 age groups is needed. Observations There are unique biological factors in children younger than 18 years and in adults older than age 50 years compared to typical adult-onset MS. These biological differences, particularly immunological and hormonal, may influence the clinical presentation of MS, resilience to neuronal injury, and differential diagnosis. While mimics of MS at the typical age at onset have been described, a comprehensive approach focused on the younger and older ends of the age spectrum has not been previously published. Conclusions and Relevance An international committee of MS experts in pediatric and adult MS was formed to provide consensus guidance on diagnostic approaches and key clinical and paraclinical red flags for non-MS diagnosis in children and older adults.
Oligoclonal bands increase the specificity of MRI criteria to predict multiple sclerosis in children with radiologically isolated syndrome
Makhani, Naila , Sıva, Aksel , Narula, Sona , Wassmer, Evangeline , Brassat, David, Brenton, J. Nicholas , Cabre, Philippe, Carra‐Dallière, Clarisse , Dubief, Françoise Durand, Inglese, Matilde , Langille, Megan, Mathey, Guillaume , Pelletier, Jean , Reich, Daniel S. , Rojas, Juan Ignacio , Shabanova, Veronika , Shapiro, Eugene D. , Stone, Robert T, Tenembaum, Sílvia , Tintoré, Mar , Uygunoğlu, Uğur , Vargas, Wendy , Venkateswaren, Sunita, Kantarci, Orhun H. , Pelletier, Daniel , Durand‐Dubief, Françoise , Carra Dallière, Clarisse , Reich, Daniel S , Tintoré, Mar , Brenton, J Nicholas , Siva, Aksel , Lebrun‐Frénay, Christine , Seze, Jerome De , Neuteboom, Rinze Frederik , Pohl, Daniela , Stone, Robert Thompson, Vermersch, Patrick , Okuda, Darin T. , Wassmer, Evangeline , Durand-Dubief, Françoise

Multiple Sclerosis Journal - Experimental, Translational and Clinical | March 21, 2019 | Volume: 5 | Issue: 1 | Pages: No page available

10.1177/2055217319836664 Get It

Background Steps towards the development of diagnostic criteria are needed for children with the radiologically isolated syndrome to identify children at risk of clinical demyelination. Objectives To evaluate the 2005 and 2016 MAGNIMS magnetic resonance imaging criteria for dissemination in space for multiple sclerosis, both alone and with oligoclonal bands in cerebrospinal fluid added, as predictors of a first clinical event consistent with central nervous system demyelination in children with radiologically isolated syndrome. Methods We analysed an international historical cohort of 61 children with radiologically isolated syndrome (≤18 years), defined using the 2010 magnetic resonance imaging dissemination in space criteria (Ped-RIS) who were followed longitudinally (mean 4.2 ± 4.7 years). All index scans also met the 2017 magnetic resonance imaging dissemination in space criteria. Results Diagnostic indices (95% confidence intervals) for the 2005 dissemination in space criteria, with and without oligoclonal bands, were: sensitivity 66.7% (38.4–88.2%) versus 72.7% (49.8–89.3%); specificity 83.3% (58.6–96.4%) versus 53.9% (37.2–69.9%). For the 2016 MAGNIMS dissemination in space criteria diagnostic indices were: sensitivity 76.5% (50.1–93.2%) versus 100% (84.6–100%); specificity 72.7% (49.8–89.3%) versus 25.6% (13.0–42.1%). Conclusions Oligoclonal bands increased the specificity of magnetic resonance imaging criteria in children with Ped-RIS. Clinicians should consider testing cerebrospinal fluid to improve diagnostic certainty. There is rationale to include cerebrospinal fluid analysis for biomarkers including oligoclonal bands in planned prospective studies to develop optimal diagnostic criteria for radiologically isolated syndrome in children.