Department of Neurology, Boston University School of Medicine, 72 E Concord Street, C-3, Boston, MA, 02118, United States.
Department of Pathology, Wayne State University School of Medicine, Detroit, MI, United States.
Seizure. 2021 Dec;93:95-101. doi: 10.1016/j.seizure.2021.09.018. Epub 2021 Oct 5.
new-onset refractory status epilepticus (NORSE) is defined as de novo refractory seizures occurring in previously healthy adults, without a clear underlying etiology. Due to refractory seizures and insufficient understanding of pathophysiology, management of these patients remains challenging and often leads to poor clinical outcomes. Various infectious and autoimmune mechanisms have been proposed but have not been validated and a large number of patients are thus labeled 'cryptogenic'. Moreover, histopathological findings have rarely been described in NORSE and are usually autopsy evaluations. In this paper, we describe the clinical correlates and histopathological findings in patients presenting with NORSE.
A case series of five patients with NORSE who underwent neurosurgical intervention and had histopathological examination during their acute clinical course.
In all patients,status epileptics was refractory to treatment with antiseizure drugs (ASDs) and anesthetic agents. Autoimmune work-up revealed elevated titer of anti-GAD antibody in one patient but was unremarkable in others. Empiric use of immunomodulation therapy in three patients did not lead to cessation of status epilepticus (SE). Due to failure of prolonged medical management, three patients underwent palliative surgery for resection of epileptogenic tissue whereas the other two had diagnostic brain biopsy. Histopathology obtained during biopsy revealed evidence of vasculitis in one and necrotizing vasculopathy in another. The patient with anti-GAD antibodies had evidence of lymphocytic infiltration in limbic structures. The remaining two had nonspecific histopathological findings.
Although our findings are limited by a small number of patients, it adds to the growing premise of NORSE being related to an underlying autoimmune process. Additional studies, especially with histopathological data are needed to better understand this devastating disorder.
新诊断的难治性癫痫持续状态(NORSE)定义为无明确潜在病因的既往健康成年人新发的耐药性癫痫发作。由于耐药性癫痫发作和对病理生理学的了解不足,这些患者的治疗仍然具有挑战性,并且常常导致不良的临床结果。已经提出了各种感染和自身免疫机制,但尚未得到验证,因此大量患者被标记为“不明原因”。此外,NORSE 中很少描述组织病理学发现,通常是尸检评估。在本文中,我们描述了具有 NORSE 表现的患者的临床相关性和组织病理学发现。
对五名接受神经外科干预且在急性临床过程中进行组织病理学检查的 NORSE 患者进行病例系列研究。
所有患者的癫痫持续状态均对抗癫痫药物(ASD)和麻醉药物的治疗耐药。自身免疫检查显示一名患者的抗 GAD 抗体滴度升高,但其他患者的自身免疫检查无明显异常。三名患者经验性使用免疫调节治疗并未导致癫痫持续状态(SE)停止。由于长期药物治疗失败,三名患者接受姑息性手术切除致痫性组织,而另外两名患者则进行了诊断性脑活检。活检获得的组织病理学显示一名患者存在血管炎证据,另一名患者存在坏死性血管病。具有抗 GAD 抗体的患者在边缘结构中存在淋巴细胞浸润的证据。其余两名患者的组织病理学发现是非特异性的。
尽管我们的研究结果受到患者数量较少的限制,但它增加了 NORSE 与潜在自身免疫过程相关的不断增长的前提。需要进行更多的研究,特别是结合组织病理学数据,以更好地了解这种破坏性疾病。