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Tumefactive MS lesions under fingolimod A case report and literature review

Journal

NEUROLOGY
Volume 81, Issue 19, Pages 1654-1658

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/01.wnl.0000435293.34351.11

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Funding

  1. European Federation of Neurological Societies
  2. UCB
  3. Biogen Idec
  4. Sanofi-Aventis
  5. Allmirall
  6. Bayer
  7. Genzyme
  8. Medtronic
  9. Merck-Serono
  10. Novartis

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Objective: To report about a possible association between fingolimod treatment and tumefactive demyelinating lesions (TDL) as seen in a patient developing repeated TDL on continued fingolimod therapy. Methods: We performed serial clinical and radiologic assessments and immunophenotyping of blood and CSF immune cells. We also present a literature review about recent similar cases. Results: Clinical course and radiologic findings were consistent with diagnosis of TDL. Immune cell phenotyping showed pronounced shifts in the immune cell composition related to fingolimod treatment. In addition, we observed a subset of highly differentiated effector cells (CD45R0negCCR7neg) within the CD8 + T-cell population, which was about 2-fold enriched in the CSF compared to the peripheral blood. Conclusion: Our observations add further evidence for the development of atypical demyelinating lesions in some patients receiving fingolimod. These might be related to a treatment-associated shift in the immunopathology of specifically susceptible individuals.

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