Extensive immune reconstitution inflammatory syndrome in Fingolimod-associated PML: a case report with 7 Tesla MRI

Tim Sinnecker1,2, Jeffrie Hadisurya3, Tilman Schneider-Hohendorf4

  • 1Department of Neurology, Universitätsspital, Basel, Switzerland.

BMC Neurology
|August 11, 2019
PubMed
Abstract

Insights

Early discontinuation of fingolimod for progressive multifocal leukoencephalopathy (PML) led to a good outcome. Immune reconstitution inflammatory syndrome (IRIS) and multiple sclerosis (MS) activity were differentiated using advanced diagnostics.

Area of Science:

  • Neuroimmunology
  • Neurology
  • Radiology

Background:

  • Progressive multifocal leukoencephalopathy (PML) is a rare but serious complication associated with fingolimod therapy.
  • Understanding PML in the context of immunomodulatory treatments is crucial for patient management.

Observation:

  • A case of asymptomatic early PML was diagnosed via routine MRI in a patient treated with fingolimod.
  • Discontinuation of fingolimod led to PML stability, but normalization of lymphocyte counts triggered immune reconstitution inflammatory syndrome (IRIS) and new multiple sclerosis (MS) activity.

Findings:

  • Advanced laboratory tests and ultrahigh field MRI were instrumental in differentiating between PML and MS.
  • Lymphocyte counts served as an indicator of immune system recovery and activity.

Implications:

  • Early detection and discontinuation of fingolimod can lead to favorable outcomes in PML.
  • Distinguishing PML-IRIS from MS is critical for appropriate treatment strategies.
  • Integrated diagnostic approaches combining imaging and laboratory findings are essential for managing complex neurological conditions.

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