Volume 35, Issue 3 pp. 290-297
Original Article
Full Access

Neuronal migration disorders: Positron emission tomography correlations

Dr. Namsoo Lee MD

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 author
Rodney A. Radtke MD

Rodney A. Radtke MD

Department of Medicine (Neurology), Duke University Medical Center, Durham, NC

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Linda Gray MD

Linda Gray MD

Department of Radiology, Duke University Medical Center, Durham, NC

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Peter C. Burger MD

Peter C. Burger MD

Department of Pathology, Duke University Medical Center, Durham, NC

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Thomas J. Montine MD, PhD

Thomas J. Montine MD, PhD

Department of Pathology, Duke University Medical Center, Durham, NC

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G. Robert DeLong MD

G. Robert DeLong MD

Department of Pediatrics, Duke University Medical Center, Durham, NC

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Darrell V. Lewis MD

Darrell V. Lewis MD

Department of Pediatrics, Duke University Medical Center, Durham, NC

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Dr. W. Jerry Oakes MD

Dr. W. Jerry Oakes MD

Department of Surgery (Neurosurgery), Duke University Medical Center, Durham, NC

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Allan H. Friedman MD

Allan H. Friedman MD

Department of Surgery (Neurosurgery), Duke University Medical Center, Durham, NC

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John M. Hoffman MD

John M. Hoffman MD

Department of Medicine (Neurology), Duke University Medical Center, Durham, NC

Department of Radiology, Duke University Medical Center, Durham, NC

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First published: March 1994
Citations: 84

Abstract

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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