Clinical and electrophysiological findings in mesial temporal lobe epilepsy with hippocampal sclerosis, based on the recent histopathological classifications

被引:12
作者
Tezer, F. Irsel [1 ]
Xasiyev, Farid [1 ]
Soylemezoglu, Figen [2 ]
Bilginer, Burcak [3 ]
Oguz, Kader Karli [4 ]
Saygi, Serap [1 ]
机构
[1] Hacettepe Univ, Fac Med, Dept Neurol, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Fac Med, Dept Pathol, Ankara, Turkey
[3] Hacettepe Univ, Fac Med, Dept Neurosurg, Ankara, Turkey
[4] Hacettepe Univ, Fac Med, Dept Radiol, Ankara, Turkey
关键词
Epilepsy; Seizure; Hippocampal sclerosis; Temporal lobe epilepsy; Pathology; Types of hippocampal sclerosis; INTERNATIONAL CONSENSUS CLASSIFICATION; RETROSPECTIVE ANALYSIS; DIAGNOSTIC METHODS; TASK-FORCE; SURGERY; COMMISSION; PREDICTORS; MORTALITY; LOBECTOMY;
D O I
10.1016/j.eplepsyres.2016.08.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Hippocampal sclerosis (HS) is a common pathology in MTLE, patients may show different surgical outcomes and clinical features. The 2013 ILAE classification subdivides HS into 3 types (HS type 1: severe neuronal loss and gliosis predominantly in CAl and CA4 regions; - HS type 2: CAl predominant; HS type 3: CA4 predominant) and includes "gliosis only, as no-HS". The association of clinical and electrophysiological findings with different HS types has not been reported previously in detail. Methods: 48 patients who had undergone temporal lobectomy with amygdalohippocampectomy due to mesial TLE-HS between February 2014 and February 2016 were included. The patients were divided into five groups: patients with HS ILAE type 1, HS ILAE type 2, HS ILAE type 3, FCD type IIIa, or gliosis/no HS. The correlation between HS ILAE types and clinical/EEG findings in patients with MTLE due to HS was investigated. Results: Of the 48 patients 30 were male. In 23 patients, the resection was on the left side (48%). Three patients had only gliosis, 25 patients had HS ILAE type 1, 7 had HS ILAE type 2, and 4 had HS ILAE type 3. Nine of the 48 patients had cortical lamination abnormalities in the temporal lobe associated with HS (FCD type IIIa). All patients were seizure free for early follow up. There was no association between type of HS in terms of duration of epilepsy, onset age of epilepsy, lateralized or localized semiological findings, or interictal/ictal EEG findings. Family history of epilepsy or SGTCSs were statistically more frequent in patients with types 2 and 3 HS and status epilepticus was more frequent in patients with HS-FCD type IIIa. Conclusion: The patients with HS types 2 and 3 have more frequent SGTCS or status epilepticus as well as increased family history of epilepsy. These findings can be helpful in understanding the epileptogenicity-prognoses of HS. (C) 2016 Elsevier B.V. All rights reserved.
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页码:50 / 54
页数:5
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