Literature DB >> 27009257

Punctate pattern: A promising imaging marker for the diagnosis of natalizumab-associated PML.

Jérôme Hodel1, Christine Darchis2, Olivier Outteryck2, Sébastien Verclytte2, Vincent Deramecourt2, Arnaud Lacour2, Marc Zins2, Jean-Pierre Pruvo2, Patrick Vermersch2, Xavier Leclerc2.   

Abstract

OBJECTIVE: To evaluate the usefulness of the punctate pattern (PP) for the diagnosis and follow-up of patients with progressive multifocal leukoencephalopathy (PML).
METHODS: A cohort of 20 consecutive patients with PML, related to natalizumab (NTZ) (n = 14) or not (n = 6), underwent 3T MRI (147 MRI examinations). MRI was available at presymptomatic (n = 9 patients), symptomatic (n = 15), immune reconstitution inflammatory syndrome (IRIS), and chronic stages (n = 20). A pathologic control group of patients without PML (n = 80), with clinically definitive multiple sclerosis or a clinically isolated syndrome suggestive of CNS demyelination, underwent the same MRI protocol. Number and appearance of punctate lesions were assessed by 3 blinded readers using T2-weighted, fluid-attenuated inversion recovery (FLAIR), and postcontrast T1-weighted images.
RESULTS: Interobserver agreement was good (κ = 0.79) (0.72-0.87). Of the 20 patients with PML, 18 had PP, including the 14 patients with NTZ-PML; none in the pathologic control group. Of the 9 presymptomatic patients with NTZ-PML, PP was observed in 7 (78% sensitive and 100% specific). Nonenhancing PP on T2-weighted/FLAIR images was detected in 13 patients with PML, exclusively at the presymptomatic or symptomatic stages (including 7 NTZ-PML), whereas enhancing PP occurred in 16 patients with PML, including 13 of the 14 patients with NTZ-PML at the IRIS stage.
CONCLUSIONS: PP is a highly specific feature of PML and may be the first imaging feature at the presymptomatic stage with potential implications in patient care. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that a PP on MRI accurately identifies patients with NTZ-PML.
© 2016 American Academy of Neurology.

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Year:  2016        PMID: 27009257     DOI: 10.1212/WNL.0000000000002586

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  18 in total

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