4.7 Article

FDG-PET/MRI coregistration improves detection of cortical dysplasia in patients with epilepsy

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NEUROLOGY
卷 71, 期 20, 页码 1594-1601

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/01.wnl.0000334752.41807.2f

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资金

  1. NIH [R01 NS38992, P05 NS02808]
  2. Ministry of Education, Culture, Sports, Science, and Technology of Japan [17689040]
  3. Japan Epilepsy Research Foundation [H16-009]
  4. Grants-in-Aid for Scientific Research [17689040] Funding Source: KAKEN

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Objective: Patients with cortical dysplasia (CD) are difficult to treat because the MRI abnormality may be undetectable. This study determined whether fluorodeoxyglucose (FDG)-PET/MRI coregistration enhanced the recognition of CD in epilepsy surgery patients. Methods: Patients from 2004-2007 in whom FDG-PET/MRI coregistration was a component of the presurgical evaluation were compared with patients from 2000-2003 without this technique. For the 2004-2007 cohort, neuroimaging and clinical variables were compared between patients with mild Palmini type I and severe Palmini type II CD. Results: Compared with the 2000-2003 cohort, from 2004-2007 more CD patients were detected, most had type I CD, and fewer cases required intracranial electrodes. From 2004-2007, 85% of type I CD cases had normal non-University of California, Los Angeles (UCLA) MRI scans. UCLA MRI identified CD in 78% of patients, and 37% of type I CD cases had normal UCLA scans. EEG and neuroimaging findings were concordant in 52% of type I CD patients, compared with 89% of type II CD patients. FDG-PET scans were positive in 71% of CD cases, and type I CD patients had less hypometabolism compared with type II CD patients. Postoperative seizure freedom occurred in 82% of patients, without differences between type I and type II CD cases. Conclusions: Incorporating fluorodeoxyglucose-PET/MRI coregistration into the multimodality presurgical evaluation enhanced the noninvasive identification and successful surgical treatment of patients with cortical dysplasia (CD), especially for the 33% of patients with nonconcordant findings and those with normal MRI scans from mild type I CD. Neurology (R) 2008; 71: 1594-1601

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