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首页> 外文期刊>Epilepsy research >Sequential prefrontal lobe volume changes and cognitive dysfunctions in children with Panayiotopoulos syndrome presenting with status epilepticus
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Sequential prefrontal lobe volume changes and cognitive dysfunctions in children with Panayiotopoulos syndrome presenting with status epilepticus

机译:伴癫痫持续状态的Panayiotopoulos综合征患儿的前额叶顺序变化和认知功能障碍

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Panayiotopoulos syndrome (PS) is usually not associated with neurodevelopmental problems. However, neuropsychological impairments may also be present in at least some of the patients with PS. On the other hand, several degrees of neuronal damage due to status epilepticus (SE) may occur in the cortex. We prospectively measured frontal and prefrontal lobe volumes using three-dimensional magnetic resonance imaging (3D-MRI)-based volumetry in patients with PS with and without SE. Moreover, the neuropsychological outcome in relation to the presence of SE in children with PS is also discussed. We studied six patients with a final diagnosis of PS, including three cases with SE and cognitive impairments/behavioral problems (SE group) and three cases without SE (non-SE group). Serial 3D-MRI studies were performed five times (at onset of clinical symptoms and 1-4 years after onset) in both the SE and non-SE patients. All patients were studied with a set of Wechsler Intelligence Scale for Children, version III (WISC-III) or Wechsler Preschool and Primary Scale of Intelligence tests and the Kaufman Assessment Battery for Children (K-ABC). Growth of the frontal and prefrontal lobes was slightly decreased for some time after SE episodes in the SE patients. Moreover, the prefrontal-to-frontal lobe volume ratio was stagnant for some time after SE in the SE patients. The scores on the neuropsychological tests were decreased in the SE patients. Moreover, the average WISC and K-ABC scores in the SE group remained low and did not reach the levels of the initial examinations. Occurrence of SE in patients with PS at least in some patients may be associated with retarded prefrontal lobe growth, which was related to neuropsychological problems and ultimately, neuropsychological outcomes. Treatment management may be required to prevent SE as much as possible to achieve optimal prognosis in PS at least in some patients.
机译:Panayiotopoulos综合征(PS)通常与神经发育问题无关。但是,至少一些PS患者也可能存在神经心理障碍。另一方面,由于癫痫持续状态(SE)引起的神经元损伤可能在皮质中发生数个程度。我们使用基于三维磁共振成像(3D-MRI)的容量法,对患有或未患有SE的PS患者前瞻性地测量了额叶和额叶的体积。此外,还讨论了PS儿童患SE的神经心理学结果。我们研究了6例最终诊断为PS的患者,包括3例有SE和认知障碍/行为问题的患者(SE组)和3例无SE的患者(非SE组)。 SE和非SE患者均进行了5次连续3D-MRI研究(临床症状发作时和发作后1-4年)。所有患者均接受了一套韦氏儿童智力量表(III版)(WISC-III)或韦氏儿童学前和初等智力量表以及考夫曼儿童评估表(K-ABC)进行研究。 SE患者发作SE后一段时间,额叶和额叶的生长略有下降。此外,SE患者SE后一段时间前额叶与额叶的体积比停滞。 SE患者的神经心理测验得分降低。此外,SE组的WISC和K-ABC平均得分仍然很低,没有达到初始检查的水平。至少在某些患者中,PS患者中SE的发生可能与前额叶生长受阻有关,这与神经心理学问题以及最终与神经心理学结果有关。至少在某些患者中,可能需要进行治疗管理以尽可能预防SE,以实现PS的最佳预后。

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