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Interictal 99Tcm HMPAO SPECT and 1H MRS in Children with Temporal Lobe Epilepsy
Authors:J. H. Cross,I. Gordon&Dagger  ,A. Connelly&dagger  ,G. D. Jackson,C. L. Johnson&Dagger  ,B. G. R. Neville,D. G. Gadian&dagger  
Affiliation:Neurosciences Unit, Institute of Child Health, Great Ormond Street Hospital for Children NHS Trust, London, England;Department of Radiology, Great Ormond Street Hospital for Children NHS Trust, London, England;Radiology and Physics Unit, Institute of Child Health, Great Ormond Street Hospital for Children NHS Trust, London, England
Abstract:Summary: Purpose: To understand the pathological basis of focal hypoperfusion seen on interictal 99Tcm hexamethylpropyleneamine oxime (HMPAO) single-photon-emission computed tomography (SPECT) in intractable temporal lobe epilepsy, and to determine why the technique may be misleading in the localization and lateralization of the seizure focus in some cases.
Methods: Interictal 99Tcm HMPAO SPECT and proton magnetic resonance spectroscopy (1H MRS) of the mesial temporal regions were performed in 14 children with intractable temporal lobe epilepsy not caused by a foreign tissue lesion.
Results: Hypoperfusion of one temporal lobe ipsilateral to the seizure focus was demonstrated in 10 (71%) of the children; 1H MRS correctly lateralised in eight of these 10. No asymmetry of perfusion of the anterior temporal regions was seen in the remaining four children; on 1H MRS, three of these were bilaterally abnormal but nonlateralising. Repeated SPECT and 1H MRS in three children demonstrated changes over time, the findings from the two techniques being consistent with each other on both the initial and the repeated scans.
Conclusions: Abnormalities demonstrated by 1H MRS correlate well with those seen on interictal SPECT and can help to understand the pathologic basis of these SPECT abnormalities. Furthermore, the presence of bilateral damage can result in an absence of perfusion asymmetry on interictal SPECT.
Keywords:Temporal lobe epilepsy    Single-photon    emission computed tomography    Proton magnetic resonance spectroscopy    Child    Hypoperfusion    Neuronal loss
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