Department of Neuropathology, University Hospital Erlangen, Erlangen, Germany.
Epilepsia. 2012 Aug;53(8):1341-8. doi: 10.1111/j.1528-1167.2012.03508.x. Epub 2012 May 29.
An International League Against Epilepsy (ILAE) consensus classification system for focal cortical dysplasias (FCDs) has been published in 2011 specifying clinicopathologic FCD variants. The aim of the present work was to microscopically assess interobserver agreement and intraobserver reproducibility for FCD categories among an international group of neuropathologists with different levels of experience and access to epilepsy surgery tissue.
Surgical FCD specimens covering a broad histopathology spectrum were retrieved from 22 patients with epilepsy. Three surgical nonepilepsy specimens served as controls. A total of 188 slides with routine or immunohistochemical stainings were digitalized with a slide scanner to allow Internet-based microscopy review. Nine experienced neuropathologists were invited to review these cases twice at a time gap of 3 months and different orders of case presentation. The 2011 ILAE FCD consensus classification served as instruction. Kappa analysis was calculated to estimate interobserver and intraobserver agreement levels. In a third evaluation round, 21 additional neuropathologists with different experience and access to epilepsy surgery reviewed the same case series.
Interobserver agreement was good (κ = 0.6360), with 84% consensus of diagnoses during the first evaluation (21 of 25 cases). Kappa values increased to 0.6532 after reevaluation, and consensus was obtained in 24 (96%) of 25 cases. Overall intraobserver reproducibility was also good (κ = 0.7824, ranging from 0.4991 to 1.000). Fewest changes in the classification were made in the FCD type II group (2.2% of 225 original diagnoses), whereas the majority of changes occurred in FCD type III (13.7% of 225 original diagnoses). In the third evaluation round, interobserver agreement was reflected by the level of experience of each neuropathologist, with κ values ranging from moderate (0.5056; high level of experience >40 cases/year) to low (0.3265; low level of experience <10 cases/year).
Our study achieved a good and reliable interobserver agreement among the group of expert neuropathologists originally involved in the ILAE FCD consensus classification system. Intraobserver reproducibility in this group was even more robust. These results showed considerable improvement compared to a previous study evaluating the 2004 Palmini FCD classification. Agreement levels were lower in our second group of neuropathologists and were related to their level of access and experience with epilepsy surgery specimens. These results suggested that the more precise ILAE definition of FCD histopathology patterns improves operational procedures in the diagnosis of FCDs. On the other hand, microscopic assessment of FCD is a challenge and requires sustained experience and teaching. The virtual slide review system allowed testing of this hypothesis and reached a widespread group of participating colleagues from different centers all over the world. We propose to further use this tool as a teaching device and also to address other epilepsy-associated entities still difficult to classify such as hippocampal sclerosis, long-term epilepsy-associated tumors, or mild malformations of cortical development (mMCDs), which were not yet covered by current ILAE classification systems.
国际抗癫痫联盟(ILAE)于 2011 年发布了局灶性皮质发育不良(FCD)的共识分类系统,具体规定了临床病理 FCD 变异。本研究的目的是通过不同经验水平和接触癫痫手术组织的国际神经病理学家小组,在微观上评估 FCD 类别的观察者间一致性和观察者内可重复性。
从 22 名癫痫患者中获取了涵盖广泛组织病理学谱的手术 FCD 标本。3 例非癫痫手术标本作为对照。共对 188 张具有常规或免疫组织化学染色的幻灯片进行数字化处理,使用幻灯片扫描仪进行基于互联网的显微镜检查。邀请 9 名经验丰富的神经病理学家在 3 个月的时间间隔和不同的病例呈现顺序下两次审查这些病例。2011 年 ILAE FCD 共识分类作为指导。计算kappa 分析以评估观察者间和观察者内的一致性水平。在第三个评估轮次中,21 名具有不同经验和接触癫痫手术的额外神经病理学家审查了相同的病例系列。
观察者间的一致性良好(κ=0.6360),在第一次评估时有 84%的诊断共识(25 例中的 21 例)。重新评估后,kappa 值增加到 0.6532,25 例中有 24 例(96%)达到共识。总体观察者内可重复性也很好(κ=0.7824,范围为 0.4991 至 1.000)。在 225 例原始诊断中,FCD II 型的分类变化最少(2.2%),而大多数变化发生在 FCD III 型(225 例原始诊断中的 13.7%)。在第三个评估轮次中,每个神经病理学家的经验水平反映了观察者间的一致性,kappa 值范围从中度(0.5056;高水平经验>40 例/年)到低度(0.3265;低水平经验<10 例/年)。
我们的研究在最初参与 ILAE FCD 共识分类系统的一组专家神经病理学家中达到了良好和可靠的观察者间一致性。该组的观察者内可重复性甚至更稳健。与之前评估 2004 年 Palmini FCD 分类的研究相比,这些结果显示出了相当大的改善。我们第二组神经病理学家的一致性水平较低,这与他们接触癫痫手术标本的水平和经验有关。这些结果表明,ILAE 对 FCD 组织病理学模式的更精确定义提高了 FCD 诊断的操作程序。另一方面,FCD 的显微镜评估是一项挑战,需要持续的经验和教学。虚拟幻灯片审查系统允许测试这一假设,并使来自世界各地不同中心的广泛参与同事受益。我们建议进一步使用该工具作为教学工具,并解决其他仍然难以分类的与癫痫相关的实体,如海马硬化、长期癫痫相关肿瘤或轻度皮质发育不良(mMCD),这些实体尚未被当前的 ILAE 分类系统涵盖。