Santagostino Barbone Alessandro, De Grandis Elisa, Giacomini Thea, Buratti Silvia, Micalizzi Camilla, Brisca Giacomo, Aiello Alessia, Micalizzi Concetta, Mancardi Maria Margherita
Department of Neuroscience, Rehabilitation, Ophthalmology, Genetic and Maternal Infantile Sciences, University of Genova, Genova, Italy.
Department of Clinical Pediatrics Sciences, Unit of Child Neuropsychiatry, Member of the ERN Epicare Network, IRCCS Istituto Giannina Gaslini, Via G Gaslini 5, Genova, 16100, Italy.
BMC Neurol. 2025 Aug 29;25(1):368. doi: 10.1186/s12883-025-04346-7.
Herpes simplex virus 1 (HSV-1) encephalitis may result in relapsing neurological symptoms secondary to immune-mediated processes, including anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. Refractory status dyskineticus (RSD), a severe subset of status dystonicus, is characterized by a hyperkinetic movement disorder phenotype alongside dystonic features. This critical condition presents substantial challenges in neurocritical care. The present case highlights the importance of prompt intervention and immunotherapy escalation in managing severe movement disorders due to pediatric autoimmune encephalitis.
A previously healthy 2-year-old boy was admitted with HSV-1 encephalitis, confirmed by brain MRI and cerebrospinal fluid (CSF) analysis. When initially treated with acyclovir, the patient achieved partial recovery but later developed encephalopathy, vomiting, behavioral regression, and severe dyskinetic movements. Upon transfer to our center, NMDAR antibodies were detected in the CSF, with no evidence of HSV reactivation. Despite first-line immunotherapy with intravenous steroids and immunoglobulins, his condition deteriorated, progressing to status dyskineticus (SD), with dystonia, hyperthermia, and hypercapnia, requiring intensive care management and mechanical ventilation. A treatment escalation regimen including both immunotherapy with rituximab, rapamycin, bortezomib, and multiple symptomatic therapies resulted in gradual improvement and resolution of the movement disorder.
This case underscores the crucial role of neurocritical care in managing refractory movement disorders associated with autoimmune encephalitis. Early recognition and immunotherapy escalation are essential to improve outcomes in children with complex, life-threatening neurological conditions. A comprehensive, multidisciplinary approach in the neurocritical care setting is key to achieving recovery and minimizing long-term neurological damage.
单纯疱疹病毒1型(HSV-1)脑炎可能导致继发于免疫介导过程的复发性神经症状,包括抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎。难治性运动障碍状态(RSD)是张力障碍状态的严重亚型,其特征是伴有张力障碍特征的运动过多障碍表型。这种危急情况在神经重症监护中带来了重大挑战。本病例强调了在治疗小儿自身免疫性脑炎所致严重运动障碍时及时干预和强化免疫治疗的重要性。
一名此前健康的2岁男孩因HSV-1脑炎入院,经脑部MRI和脑脊液(CSF)分析确诊。最初用阿昔洛韦治疗时,患者部分恢复,但后来出现脑病、呕吐、行为倒退和严重的运动障碍。转至我们中心后,在脑脊液中检测到NMDAR抗体,无HSV再激活的证据。尽管采用静脉注射类固醇和免疫球蛋白进行一线免疫治疗,但其病情仍恶化,进展为运动障碍状态(SD),伴有肌张力障碍、高热和高碳酸血症,需要重症监护管理和机械通气。包括使用利妥昔单抗、雷帕霉素、硼替佐米进行免疫治疗以及多种对症治疗的强化治疗方案使运动障碍逐渐改善并得到缓解。
本病例强调了神经重症监护在治疗与自身免疫性脑炎相关的难治性运动障碍中的关键作用。早期识别和强化免疫治疗对于改善患有复杂、危及生命的神经疾病儿童的预后至关重要。在神经重症监护环境中采用全面、多学科的方法是实现康复并将长期神经损伤降至最低的关键。