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      Temporal pole signal abnormality on MR imaging in temporal lobe epilepsy with hippocampal sclerosis: a fluid-attenuated inversion-recovery study Translated title: Anormalidade de sinal na imagem por RM do pólo temporal na epilepsia do lobo temporal com esclerose hipocampal: um estudo pela seqüência inversão recuperação com supressão da água livre (FLAIR)

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          Abstract

          OBJECTIVE: To determine the frequency and regional involvement of temporal pole signal abnormality (TPA) in patients with hippocampal sclerosis (HS) using fluid-attenuated inversion-recovery (FLAIR) MR imaging, and to correlate this feature with history. METHOD: Coronal FLAIR images of the temporal pole were assessed in 120 patients with HS and in 30 normal subjects, to evaluate gray-white matter demarcation. RESULTS: Ninety (75%) of 120 patients had associated TPA. The HS side made difference regarding the presence of TPA, with a left side prevalence (p=0.04, chi2 test). The anteromedial zone of temporal pole was affected in 27 (30%) out of 90 patients. In 63 (70%) patients the lateral zone were also affected. Patients with TPA were younger at seizure onset (p=0.018), but without association with duration of epilepsy. CONCLUSION: Our FLAIR study show temporal pole signal abnormality in 3/4 of patients with HS, mainly seen on the anteromedial region, with a larger prevalence when the left hippocampus was involved.

          Translated abstract

          OBJETIVO: Determinar a freqüência e o envolvimento regional da anormalidade de sinal do pólo temporal (APT) em pacientes com esclerose hipocampal (EH) utilizando seqüência inversão recuperação com supressão da água (FLAIR) por RM, e correlacioná-la com a história. MÉTODO: Foram analisadas as imagens coronais FLAIR dos pólos temporais de 120 pacientes com EH e de 30 indivíduos normais, para avaliar a demarcação entre substâncias branca e cinzenta. RESULTADOS: Noventa (75%) dos 120 pacientes tinham APT associada. Houve prevalência do lado esquerdo (p=0.04, chi2 teste) na relação entre APT e o lado da EH. A zona ântero-medial estava acometida em 27 (30%) destes pacientes. Em 63 (70%) pacientes também a zona lateral estava acometida. Pacientes com APT apresentaram início da epilepsia quando mais jovens (p=0.018), porém sem associação com a sua duração. CONCLUSÃO: A seqüência FLAIR mostra haver ATP em 3/4 dos pacientes com EH, principalmente na região ântero-medial, com maior prevalência quando o hipocampo esquerdo estava envolvido.

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          Whole-brain voxel-based statistical analysis of gray matter and white matter in temporal lobe epilepsy.

          Volumetric MRI studies based on manual labeling of selected anatomical structures have provided in vivo evidence that brain abnormalities associated with temporal lobe epilepsy (TLE) extend beyond the hippocampus. Voxel-based morphometry (VBM) is a fully automated image analysis technique allowing identification of regional differences in gray matter (GM) and white matter (WM) between groups of subjects without a prior region of interest. The purpose of this study was to determine whole-brain GM and WM changes in TLE and to investigate the relationship between these abnormalities and clinical parameters. We studied 85 patients with pharmacologically intractable TLE and unilateral hippocampal atrophy and 47 age- and sex-matched healthy control subjects. The seizure focus was right sided in 40 patients and left sided in 45. Student's t test statistical maps of differences between patients' and controls' GM and WM concentrations were obtained using a general linear model. A further regression against duration of epilepsy, age of onset, presence of febrile convulsions, and secondary generalized seizures was performed with the TLE population. Voxel-based morphometry revealed that GM pathology in TLE extends beyond the hippocampus involving other limbic areas such as the cingulum and the thalamus, as well as extralimbic areas, particularly the frontal lobe. White matter reduction was found only ipsilateral to the seizure focus, including the temporopolar, entorhinal, and perirhinal areas. This pattern of structural changes is suggestive of disconnection involving preferentially frontolimbic pathways in patients with pharmacologically intractable TLE.
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            ILAE Commission Report. Mesial temporal lobe epilepsy with hippocampal sclerosis.

            Experts discussed the definition, natural history, pathologic features, pathogenesis, electroclinical, neurophysiological, neuropsychological, structural and functional imaging findings, as well as surgical outcome in mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS). After a long-lasting consensus process the ILAE Commission Neurosurgery of epilepsy accepted the resulting conclusions as state-of-the art report on MTLE-HS. The majority of contributors considered MTLE-HS to represent a sufficient cluster of signs and symptoms to make up a syndromic diagnostic entity.
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              The right brain hemisphere is dominant in human infants.

              The development of functional brain asymmetry during childhood is confirmed by changes in cerebral blood flow measured at rest using dynamic single photon emission computed tomography. Between 1 and 3 years of age, the blood flow shows a right hemispheric predominance, mainly due to the activity in the posterior associative area. Asymmetry shifts to the left after 3 years. The subsequent time course of changes appear to follow the emergence of functions localized initially on the right, but later on the left hemisphere (i.e. visuospatial and later language abilities). These findings support the hypothesis that, in man, the right hemisphere develops its functions earlier than the left.
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                Author and article information

                Journal
                anp
                Arquivos de Neuro-Psiquiatria
                Arq. Neuro-Psiquiatr.
                Academia Brasileira de Neurologia - ABNEURO (São Paulo, SP, Brazil )
                0004-282X
                1678-4227
                September 2007
                : 65
                : 3a
                : 553-560
                Affiliations
                [06] orgnameUNIFESP orgdiv1EPM orgdiv2Departamento de Diagnóstico por Imagem
                [04] orgnameUNIFESP orgdiv1EPM orgdiv2Departamento de Neurologia e Neurocirurgia
                [02] orgnameUNIFESP orgdiv1EPM orgdiv2Departamento de Diagnóstico por Imagem
                [03] orgnameUNIFESP orgdiv1EPM orgdiv2Departamento de Neurologia e Neurocirurgia
                [01] São Paulo SP orgnameUniversidade Federal de São Paulo orgdiv1Escola Paulista de Medicina orgdiv2Departamento de Diagnóstico por Imagem Brasil
                [05] orgnameUNIFESP orgdiv1EPM orgdiv2Departamento de Diagnóstico por Imagem
                [07] orgnameUNIFESP orgdiv1EPM orgdiv2Departamento de Neurologia e Neurocirurgia
                Article
                S0004-282X2007000400001 S0004-282X(07)06500301
                c15022b4-8156-483d-a560-424eb92a26b0

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 07 March 2007
                : 07 May 2007
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 24, Pages: 8
                Product

                SciELO Brazil

                Self URI: Full text available only in PDF format (EN)

                ressonância magnética,magnetic resonance imaging,temporal pole,hippocampal sclerosis,temporal lobe epilepsy,epilepsy,pólo temporal,esclerose hipocampal,epilepsia do lobo temporal,epilepsia

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