Tezer F Irsel, Xasiyev Farid, Soylemezoglu Figen, Bilginer Burcak, Oguz Kader Karli, Saygi Serap
Hacettepe University, Faculty of Medicine, Dept. of Neurology, Ankara, Turkey.
Hacettepe University, Faculty of Medicine, Dept. of Neurology, Ankara, Turkey.
Epilepsy Res. 2016 Nov;127:50-54. doi: 10.1016/j.eplepsyres.2016.08.012. Epub 2016 Aug 16.
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 CA1 and CA4 regions; - HS type 2: CA1 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.
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.
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.
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.
海马硬化(HS)是内侧颞叶癫痫(MTLE)的常见病理表现,患者可能表现出不同的手术结果和临床特征。2013年国际抗癫痫联盟(ILAE)分类将HS分为3型(HS 1型:主要在CA1和CA4区域有严重神经元丢失和胶质增生;HS 2型:以CA1为主;HS 3型:以CA4为主),并包括“仅有胶质增生,为非HS”。此前尚未详细报道不同HS类型与临床及电生理结果之间的关联。
纳入2014年2月至2016年2月期间因内侧颞叶癫痫 - 海马硬化接受颞叶切除术加杏仁核海马切除术的48例患者。患者分为五组:ILAE 1型HS患者、ILAE 2型HS患者、ILAE 3型HS患者、IIIa型局灶性皮质发育不良(FCD)患者或胶质增生/无HS患者。研究HS的ILAE类型与因HS导致的MTLE患者临床/脑电图结果之间的相关性。
48例患者中30例为男性。23例患者的切除部位在左侧(48%)。3例患者仅有胶质增生,25例患者为ILAE 1型HS,7例为ILAE 2型HS,4例为ILAE 3型HS。48例患者中有9例在与HS相关的颞叶存在皮质分层异常(IIIa型FCD)。所有患者在早期随访中均无癫痫发作。在癫痫持续时间、癫痫发作起始年龄、偏侧或定位性发作症状学表现或发作间期/发作期脑电图结果方面,HS类型之间无关联。癫痫家族史或全面性强直阵挛发作(SGTCS)在2型和3型HS患者中在统计学上更为常见,癫痫持续状态在HS - IIIa型FCD患者中更为常见。
2型和3型HS患者的SGTCS或癫痫持续状态更为常见,癫痫家族史也增加。这些发现有助于理解HS的致痫性及预后。