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      Leptomeningeal enhancement on post-contrast FLAIR images for early diagnosis of Susac syndrome

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          Abstract

          Background:

          Leptomeningeal enhancement (LME) is a key feature of Susac syndrome (SuS) but is only occasionally depicted on post-contrast T1-weighted images (T1-WI).

          Objective:

          As post-contrast fluid-attenuated inversion recovery (FLAIR) may be more sensitive, our aim was to assess LME in SuS on this sequence.

          Methods:

          From 2010 to 2020, 20 patients with definite SuS diagnosis were retrospectively enrolled in this multicentre study. Two radiologists independently assessed the number of LME on post-contrast FLAIR and T1-WI acquisitions performed before any treatment. A chi-square test was used to compare both sequences and the interrater agreement was calculated.

          Results:

          Thirty-five magnetic resonance imagings (MRIs) were performed before treatment, including 19 post-contrast FLAIR images in 17 patients and 25 post-contrast T1-WI in 19 patients. In terms of patients, LME was observed on all post-contrast FLAIR, contrary to post-contrast T1-WI (17/17 (100%) vs. 15/19 (79%), p < 0.05). In terms of sequences, LME was observed on all post-contrast FLAIR, contrary to post-contrast T1-WI (19/19 (100%) vs. 16/25 (64%), p < 0.005). LME was disseminated at both supratentorial (19/19) and infratentorial (18/19) levels on post-contrast FLAIR, contrary to post-contrast T1-WI (3/25 and 9/25, respectively). Interrater agreement was excellent for post-contrast FLAIR (κ = 0.95) but only moderate for post-contrast T1-WI (κ = 0.61).

          Conclusion:

          LME was always observed and easily visible on post-contrast FLAIR images prior to SuS treatment. In association with other MRI features, it is highly indicative of SuS.

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          Most cited references19

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          Characteristics of Susac syndrome: a review of all reported cases.

          In Susac syndrome, occlusions of microvessels--presumed to be mediated by an autoimmune response to an as yet unknown antigen--lead to a characteristic clinical triad of CNS dysfunction, branch retinal artery occlusions, and sensorineural hearing impairment. Susac syndrome is considered a rare but important differential diagnosis in numerous neurological, psychiatric, ophthalmological, and ear, nose and throat disorders. Improved understanding of this disorder is crucial, therefore, to ensure that patients receive appropriate treatment and care. Current knowledge on Susac syndrome is largely based on reports of single patients, small case series, and nonsystematic reviews. The aim of this Review is to extend these previous, primarily anecdotal findings by compiling data from all 304 cases of Susac syndrome that have been published worldwide, which were identified following a literature search with predefined search, inclusion and exclusion criteria. From this data, we present an overview of demographic, clinical and diagnostic data on Susac syndrome, providing a reliable basis for our current understanding of this rare disease. Where possible, we make recommendations for clinical diagnosis, differential diagnosis, and management of patients with suspected Susac syndrome.
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            Gadolinium-based MRI characterization of leptomeningeal inflammation in multiple sclerosis.

            To determine the frequency and nature of leptomeningeal contrast enhancement in multiple sclerosis (MS) via in vivo 3-tesla postcontrast T2-weighted, fluid-attenuated inversion recovery (FLAIR) MRI and 7-tesla postmortem MRI-pathology correlation.
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              MRI findings in Susac's syndrome.

              Susac syndrome (SS) is a self-limited syndrome, presumably autoimmune, consisting of a clinical triad of encephalopathy, branch retinal artery occlusions, and hearing loss. All three elements of the triad may not be present or recognized, and MR imaging is often necessary to establish the diagnosis. To determine the spectrum of abnormalities on MRI in SS. The authors reviewed the MR images of 27 previously unreported patients with the clinical SS triad, and 51 patients from published articles in which the MR images were depicted or reported. All 27 patients had multifocal supratentorial white matter lesions including the corpus callosum. The deep gray nuclei (basal ganglia and thalamus) were involved in 19 (70%). Nineteen (70%) also had parenchymal enhancement and 9 (33%) had leptomeningeal enhancement. Of the 51 cases from the literature, at least 32 had callosal lesions. The authors could not determine the presence of callosal lesions in 18 of these patients, and only one was reported to have a normal MRI at the onset of encephalopathy. The MR scans in SS show a rather distinctive pattern of supratentorial white matter lesions that always involve the corpus callosum. There is often deep gray matter, posterior fossa involvement, and frequent parenchymal with occasional leptomeningeal enhancement. The central callosal lesions differ from those in demyelinating disease, and should support the diagnosis of SS in patients with at least two of the three features of the clinical triad.
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                Author and article information

                Contributors
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                Journal
                Multiple Sclerosis Journal
                Mult Scler
                SAGE Publications
                1352-4585
                1477-0970
                February 2022
                May 14 2021
                February 2022
                : 28
                : 2
                : 189-197
                Affiliations
                [1 ]Department of Neuroradiology, Hôpital Purpan, Toulouse, France
                [2 ]Department of Neurology, Hôpital Purpan, Toulouse, France
                [3 ]Department of Neuroradiology, Fondation Ophtalmologique Adolphe de Rothschild, Paris, France
                [4 ]Department of Neurology, Fondation Ophtalmologique Adolphe de Rothschild, Paris, France
                [5 ]Department of Neuroradiology, Hôpital Gui De Chauliac, Montpellier, France
                [6 ]Department of Neurology, Hôpital Gui De Chauliac, Montpellier, France
                [7 ]Department of Neuroradiology, Hôpital civil de Lyon, Lyon, France
                [8 ]Department of Neurology, Hôpital civil de Lyon, Lyon, France
                [9 ]Department of Neuroradiology, Hôpital Pellegrin, Bordeaux, France
                [10 ]Department of Neurology, Hôpital de Hautepierre, Strasbourg, France
                [11 ]Department of Neuroradiology, Hôpital de Hautepierre, Strasbourg, France
                [12 ]Department of Neurology, Hôpital Pellegrin, Bordeaux, France
                [13 ]Department of Ophthalmology, Hôpital Purpan, Toulouse, France
                Article
                10.1177/13524585211012349
                33988466
                b089296b-27e1-48b9-ae31-81ae3e1cf570
                © 2022

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