Zheng Feixia, Ye Xiuyun, Shi Xulai, Poonit Neha Devi, Lin Zhongdong
Department of Pediatric Neurology, The Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Department of Pediatrics, The Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Front Neurol. 2018 Feb 22;9:81. doi: 10.3389/fneur.2018.00081. eCollection 2018.
The use of botulinum neurotoxin serotype A (BoNT-A) injections for the treatment of orofacial dyskinesia secondary to anti--methyl-d-aspartate receptor (NMDAR) encephalitis is rarely reported. Here, we report a case of an urgent, successful management of severe orofacial dyskinesia in an 8-year-old girl with anti-NMDAR encephalitis using BoNT-A injection. The patient presented with unilateral paroxysmal movement disorder progressing to generalized dystonia and repetitive orofacial dyskinesia. Diagnosis was confirmed by the presence of NMDAR antibodies in serum and cerebrospinal fluid. The orofacial dyskinesia worsened despite the aggressive use of first-line immunotherapy and second-line immunotherapy (rituximab), and resulted in a potentially fatal self-inflicted oral injury. We urgently attempted symptomatic management using BoNT-A injections in the masseter, and induced muscle paralysis using vecuronium. The patient's severe orofacial dyskinesia was controlled. We observed the effects of the BoNT-A injections and a tapering off of the effects of vecuronium 10 days after the treatment. The movement disorder had improved significantly 4 weeks after the first administration of rituximab. The injection of BoNT-A into the masseter may be an effective treatment for medically refractory orofacial dyskinesia in pediatric patients with anti-NMDAR encephalitis. We propose that the use of BoNT-A injections should be considered early to avoid self-inflicted oral injury due to severe refractory orofacial dyskinesia in patients with anti-NMDAR encephalitis.
肉毒杆菌神经毒素A(BoNT-A)注射用于治疗抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎继发的口面部运动障碍鲜有报道。在此,我们报告一例8岁抗NMDAR脑炎女孩严重口面部运动障碍的紧急且成功治疗案例,使用了BoNT-A注射。患者最初表现为单侧阵发性运动障碍,进而发展为全身性肌张力障碍和重复性口面部运动障碍。血清和脑脊液中存在NMDAR抗体确诊了该疾病。尽管积极使用一线免疫疗法和二线免疫疗法(利妥昔单抗),口面部运动障碍仍恶化,并导致了可能致命的自伤性口腔损伤。我们紧急尝试在咬肌使用BoNT-A注射进行对症治疗,并使用维库溴铵诱导肌肉麻痹。患者严重的口面部运动障碍得到了控制。治疗10天后,我们观察到了BoNT-A注射的效果以及维库溴铵效果的逐渐消退。首次使用利妥昔单抗4周后,运动障碍有显著改善。向咬肌注射BoNT-A可能是治疗抗NMDAR脑炎儿科患者药物难治性口面部运动障碍的有效方法。我们建议应尽早考虑使用BoNT-A注射,以避免抗NMDAR脑炎患者因严重难治性口面部运动障碍导致自伤性口腔损伤。