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Markoula et al.                                                                                                                                                 Restricted diffusiuon in mulltpile sclerosis lesions














           Figure 1: (A) Axial T2-weighted image reveals a high signal periventricular lesion; (B) axial T1-weighted image shows peripheral open ring
           enhancement after contrast administration; (C) apparent diffusion coefficient map shows restricted diffusion at the periphery of the lesion












           Figure 2: (A) Axial T2-weighted image reveals a high signal lesion in the centrum semiovale; (B) axial T1-weighted image shows mild
           enhancement after contrast administration; (C) apparent diffusion coefficient map shows restricted diffusion at the periphery of the lesion
           the RRMS diagnosis followed by the performance of   ADLRD the restricted diffusion remains for at least
           an MRI and the symptoms which corresponded to      13 days, as reported by Balashov et al. [1]
           ADLRD,  were  the  first  indications  of  MS  symptoms.
           The patients with the established diagnosis of MS   It  is  suggested  that  ADLRD  may  represent  a
           received intravenous corticosteroids prior to MRI   new variant of MS and possible mechanisms of
           performance.                                       inflammatory cascades in MS should be investigated,
                                                              such as early leukocyte migration, cytokines effects
           An MRI was performed within one week from          on oligodendrocytes, astrocytes or microglia within
           the  onset  of  symptoms  onset  and  five  acute   the periventricular white matter of a developing
           demyelinating lesions, one in each patient, were   lesion. [1,4,5]
           demonstrated in the centrum cemiovale and in the
           periventricular region.  The diameter of the lesions   Prospective studies with a large number of patients
           was 12-25 mm.  The lesions exhibited restricted    are required to better characterize these lesions and
           diffusion at their periphery [(1.2-1.6) × 10  mm /s],   monitor the clinical course of MS patients with ADLRD.
                                                        2
                                                  -3
           with reduced signal on ADC maps [Figures 1 and 2].
           Four of the lesions showed peripheral enhancement
           on  T1WI sequences after contrast administration   DECLARATIONS
           [Figures 1 and 2].
                                                              Authors’ contributions
           Selected clinical MS cases with ADLRD are reported   Writing the paper: S. Markoula, A. Zikou
           in the literature, [3,4]  with the restriction of the diffusion   Reviewing patients’ data: S. Markoula
           involving either the entire lesion or part of the lesion.    Reviewing MRI imaging data: A. Zikou, P. Margariti
                                                          [1]
           In our case series the restriction was confined to the   Editing the paper: M. Argyropoulou, A.P. Kyritsis
           periphery of the lesions, sparing the central area,
           which were detected one week after the onset of    Financial support and sponsorship
           symptoms.  It  is  uncertain  whether  the  ADLRD,   None.
           that  do  not  enhance,  represent  a  phase  of ADLRD
           development before or after the potential contrast   Conflicts of interest
           enhancement or whether this lesion never enhanced.  There are no conflicts of interest.

           ADLRD  is  a  new  diagnostic  challenge  in  young   Patient consent
           patients.  In  acute  stroke  cases  the  ADC  maps   Not applicable.
           show  restricted  diffusion  the  first  2  days  and
           pseudo-normalization between 7-10 days, without    Ethics approval
           enhancement after gadolinium administration.  On   Not applicable.
                                                      [2]
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