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Abstract

The incidental finding of magnetic resonance imaging changes suggestive of multiple sclerosis in individuals with no clinical symptoms of multiple sclerosis has been termed the radiologically isolated syndrome (RIS). RIS in adults carries a 30% risk of a first clinical attack within 5 years. Here, we discuss the features of pediatric RIS and propose an investigational and follow-up algorithm.

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Notes

  1. 1.

    Barkhof Criteria for DIS: (1) at least nine T2 hyperintense lesions or one gadolinium-enhancing lesion, (2) at least three periventricular lesions, (3) at least one infratentorial lesion, (4) at least one juxtacortical lesion [6].

References

  1. Engell T. A clinical patho-anatomical study of clinically silent multiple sclerosis. Acta Neurol Scand. 1989;79(5):428–30.

    Article  CAS  PubMed  Google Scholar 

  2. Okuda DT, Mowry EM, Beheshtian A, Waubant E, Baranzini SE, Goodin DS, Hauser SL, Pelletier D. Incidental MRI anomalies suggestive of multiple sclerosis: the radiologically isolated syndrome. Neurology. 2009;72(14):800–5.

    Article  CAS  PubMed  Google Scholar 

  3. Lebrun C, Bensa C, Debouverie M, Wiertlevski S, Brassat D, et al. Association between clinical conversion to multiple sclerosis in radiologically isolated syndrome and magnetic resonance imaging, cerebrospinal fluid, and visual evoked potential. Arch Neurol. 2009;66(7):841–6.

    Article  PubMed  Google Scholar 

  4. Okuda DT, Mowry EM, Cree BAC, Crabtree EC, Goodin DS, Waubant E, Pelletier D. Asymptomatic spinal cord lesions predict disease progression in radiologically isolated syndrome. Neurology. 2011;76(8):686–92.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Okuda DT, Siva A, Kantarci O, Inglese M, Katz I, et al. Radiologically isolated syndrome: 5-year risk for an initial clinical event. PLoS One. 2014;9(3):e90509.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Barkhof F, Filippi M, Miller DH, et al. Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis. Brain. 1997;120(11):2059–69.

    Article  PubMed  Google Scholar 

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Correspondence to Katherine DeStefano M.D., M.S. .

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DeStefano, K., Makhani, N. (2017). Radiologically Isolated Syndrome. In: Waubant, E., Lotze, T. (eds) Pediatric Demyelinating Diseases of the Central Nervous System and Their Mimics. Springer, Cham. https://doi.org/10.1007/978-3-319-61407-6_8

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  • DOI: https://doi.org/10.1007/978-3-319-61407-6_8

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-61405-2

  • Online ISBN: 978-3-319-61407-6

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