Department of Neurology, Govind Ballabh Pant Postgraduate Institute of Medical Education and Research, New Delhi, India.
Neurol India. 2018 Jan-Feb;66(1):71-76. doi: 10.4103/0028-3886.222872.
Despite being the most common cause of cranial dystonia, Meige's syndrome remains a rare clinical entity. Characterized by blepharospasm and orofacial dystonia, patients suffering from Meige's syndrome benefit from the injection of botulinum toxin (BTX).
As the majority of the studies tend to discuss Meige's syndrome with blepharospasm patients, there is a paucity of case-based studies dealing exclusively with this syndrome. Hence, we intended to characterize and define the evolution of this syndrome and objectively determine the response of the patients suffering from this entity to BTX therapy.
Eight patients with Meige's syndrome who had never been injected with BTX in the past were evaluated at our movement disorder clinic using a structured questionnaire. Videotaping of abnormal movements was done for 5 minutes before the BTX injection and at a 1-month follow-up. All patients received electromyography-guided injection of BTX and the dosage was decided using clinical evaluation. Their demography, clinical features, and treatment response to BTX were analyzed using the "Burke-Fahn-Marsden dystonia rating scale" (BFMDRS) before injection and at a 1-month follow-up.
The peak age of symptom onset was 46.4 years with a male: female ratio of 1:1. The average duration of symptoms was 6.43 years. Majority of the patients (6/8) manifested their disease with blepharospasm, including five patients who had clonic blepharospasm. Lingual dystonia (6/8) and pharyngeal involvement (4/8) were commonly noted. Sensory tricks were present in all, with placement of the fingers over eyelids being the commonest trick (7/8). The average BTX dose administered was 51.58 units, and the peak onset of relief was noted at 8.62 days after the injection. The duration of the effect lasted for 82.5 days on an average. Only one patient reported mild weakness of the muscles of mastication following BTX injection. The average BFMDRS improved from the preprocedural score of 25.06 to 13.12 following the BTX injection.
In this series exclusively dealing with Meige's syndrome patients, tongue involvement was found to be very common (6/8, 75%), and the response to the first dose of BTX treatment was found to be excellent without the occurrence of any major side effects.
尽管梅杰综合征是颅部肌张力障碍最常见的病因,但它仍是一种罕见的临床病症。其特征为眼睑痉挛和口面肌张力障碍,梅杰综合征患者从肉毒杆菌毒素(BTX)注射中获益。
由于大多数研究倾向于讨论伴眼睑痉挛的梅杰综合征患者,因此专门针对该综合征的病例研究很少。因此,我们旨在描述和定义该综合征的演变,并客观地确定患有该病症的患者对 BTX 治疗的反应。
在我们的运动障碍诊所,对从未接受过 BTX 注射的 8 名梅杰综合征患者使用结构化问卷进行评估。在 BTX 注射前和 1 个月随访时进行 5 分钟的异常运动录像。所有患者均接受肌电图引导的 BTX 注射,剂量根据临床评估确定。在注射前和 1 个月随访时,使用“Burke-Fahn-Marsden 肌张力障碍评定量表”(BFMDRS)分析患者的人口统计学、临床特征和 BTX 治疗反应。
症状发作的峰值年龄为 46.4 岁,男女比例为 1:1。平均症状持续时间为 6.43 年。大多数患者(6/8)以眼睑痉挛起病,其中 5 例为阵挛性眼睑痉挛。舌部肌张力障碍(6/8)和咽部受累(4/8)很常见。所有患者均有感觉诡计,其中最常见的是将手指放在眼睑上(7/8)。平均注射 BTX 剂量为 51.58 单位,注射后 8.62 天达到缓解高峰。平均效应持续时间为 82.5 天。仅 1 例患者在 BTX 注射后报告咀嚼肌轻度无力。BTX 注射后,BFMDRS 平均从术前的 25.06 分提高到 13.12 分。
在本系列专门针对梅杰综合征患者的研究中,发现舌部受累非常常见(6/8,75%),且首次 BTX 治疗的效果极佳,无任何严重不良反应发生。