2015
DOI: 10.1016/j.eplepsyres.2015.02.013
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Temporopolar blurring in temporal lobe epilepsy with hippocampal sclerosis and long-term prognosis after epilepsy surgery

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Cited by 22 publications
(49 citation statements)
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“…In line with the range of frequencies reported in literature [15,17,24,42], temporopolar abnormalities were observed in more than half of patients, and were always ipsilateral to HS [17,19,22,42,43]. Therefore, they may play a role in lateralizing the temporal epileptogenesis [20,44].…”
Section: Discussionsupporting
confidence: 82%
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“…In line with the range of frequencies reported in literature [15,17,24,42], temporopolar abnormalities were observed in more than half of patients, and were always ipsilateral to HS [17,19,22,42,43]. Therefore, they may play a role in lateralizing the temporal epileptogenesis [20,44].…”
Section: Discussionsupporting
confidence: 82%
“…HS was qualitatively diagnosed by means of the comparative visual detection of atrophy and loss of definition of the internal structures of the hyppocampal formation and increased signal intensity in the T2-weighted images. According to Garbelli et al [22] and Naves et al [24], the criteria for TB definition were increased signal intensity in the white matter together with loss of grey/white matter demarcation of the temporal pole on coronal T2-weighted and FLAIR images (Fig. 1).…”
Section: Preoperative 15 T Magnetic Resonance Imagingmentioning
confidence: 99%
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“…The extensive temporopolar FLAIR changes and blurring of the gray–white matter boundary quantified here may be revealing subtle, widespread ipsi‐lesional pathological changes corresponding to the nonspecific histological changes seen in the resected specimens, such as subpial (Chaslin's) gliosis in the gray matter and perivascular glial clustering and perivascular lymphocytes in the white matter. In adults, HS is often observed in conjunction with temporopolar T2/FLAIR signal abnormalities 33, 34. Our recent study of neocortical changes in adults with TLE showed a paralimbic distribution of FLAIR hyperintensities and indicated a vulnerability of cortex with similar intracortical tissue composition to FLAIR signal hyperintensities.…”
Section: Discussionmentioning
confidence: 84%