Neuronal migration disorders: Positron emission tomography correlations
Corresponding Author
Dr. Namsoo Lee MD
Department of Medicine (Neurology), Duke University Medical Center, Durham, NC
Division of Neurology, P.O. Box 3678, Duke University Medical Center, Durham, NC 27710Search for more papers by this authorRodney A. Radtke MD
Department of Medicine (Neurology), Duke University Medical Center, Durham, NC
Search for more papers by this authorLinda Gray MD
Department of Radiology, Duke University Medical Center, Durham, NC
Search for more papers by this authorPeter C. Burger MD
Department of Pathology, Duke University Medical Center, Durham, NC
Search for more papers by this authorThomas J. Montine MD, PhD
Department of Pathology, Duke University Medical Center, Durham, NC
Search for more papers by this authorG. Robert DeLong MD
Department of Pediatrics, Duke University Medical Center, Durham, NC
Search for more papers by this authorDarrell V. Lewis MD
Department of Pediatrics, Duke University Medical Center, Durham, NC
Search for more papers by this authorDr. W. Jerry Oakes MD
Department of Surgery (Neurosurgery), Duke University Medical Center, Durham, NC
Search for more papers by this authorAllan H. Friedman MD
Department of Surgery (Neurosurgery), Duke University Medical Center, Durham, NC
Search for more papers by this authorJohn M. Hoffman MD
Department of Medicine (Neurology), Duke University Medical Center, Durham, NC
Department of Radiology, Duke University Medical Center, Durham, NC
Search for more papers by this authorCorresponding Author
Dr. Namsoo Lee MD
Department of Medicine (Neurology), Duke University Medical Center, Durham, NC
Division of Neurology, P.O. Box 3678, Duke University Medical Center, Durham, NC 27710Search for more papers by this authorRodney A. Radtke MD
Department of Medicine (Neurology), Duke University Medical Center, Durham, NC
Search for more papers by this authorLinda Gray MD
Department of Radiology, Duke University Medical Center, Durham, NC
Search for more papers by this authorPeter C. Burger MD
Department of Pathology, Duke University Medical Center, Durham, NC
Search for more papers by this authorThomas J. Montine MD, PhD
Department of Pathology, Duke University Medical Center, Durham, NC
Search for more papers by this authorG. Robert DeLong MD
Department of Pediatrics, Duke University Medical Center, Durham, NC
Search for more papers by this authorDarrell V. Lewis MD
Department of Pediatrics, Duke University Medical Center, Durham, NC
Search for more papers by this authorDr. W. Jerry Oakes MD
Department of Surgery (Neurosurgery), Duke University Medical Center, Durham, NC
Search for more papers by this authorAllan H. Friedman MD
Department of Surgery (Neurosurgery), Duke University Medical Center, Durham, NC
Search for more papers by this authorJohn M. Hoffman MD
Department of Medicine (Neurology), Duke University Medical Center, Durham, NC
Department of Radiology, Duke University Medical Center, Durham, NC
Search for more papers by this authorAbstract
We analyzed the interictal [18F]fluoro-2-deoxy-D-glucose positron emission tomography (PET) findings of 17 epileptic patients with neuronal migration disorders (NMDs). Fifteen patients had abnormal PET findings, i.e., focal hypometabolism in 9 patients and displaced metabolic activity of normal gray matter in 6. All 15 patients had magnetic resonance imaging (MRI) abnormalities; however, PET abnormality assisted in the identification of NMDs on MRI in 3 patients. Two patients with negative MRI also had negative PET studies. PET hypometabolism appeared to correlate with severity of neuronal dysgenesis or temporal lobe involvement, or both. Displaced metabolic activity of gray matter is regarded as a unique interictal [18F]fluoro-2-deoxy-D-glucose–PET finding in NMD. This study demonstrates variable metabolic patterns in NMD and that PET may be a useful complement to MRI in the evaluation of NMD.
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