Tan E K, Jankovic J
Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine, Houston, TX 77030, USA.
J Neurol Neurosurg Psychiatry. 2000 Feb;68(2):186-90. doi: 10.1136/jnnp.68.2.186.
Most patients with tardive dystonia have a focal onset involving the cranial-cervical region. Because of its resemblance to idiopathic cranial dystonia, a common form of dystonia, it often poses a diagnostic problem. To compare clinical features and response to botulinum toxin (BTX) injections between patients with tardive and idiopathic oromandibular dystonia (OMD).
Patients seen in a movement disorder clinic who satisfied the inclusion criteria for tardive or idiopathic OMD were studied. The clinical variables and responses to BTX between the two groups of patients were compared. In the tardive group, we also compared the clinical variables between those with oro-facial-lingual stereotypies, and those without.
Twenty four patients with tardive OMD and 92 with idiopathic OMD were studied. There were no differences in the demographic characteristics. Most were women, with duration of symptoms longer than 8 years. The mean duration of neuroleptic exposure was 7.1 (SD 7.9) years. Jaw closure was the most frequent subtype of OMD (tardive=41.7%, idiopathic=51.1%). Idiopathic patients were more likely to have coexistent cervical dystonia (p<0.05), whereas isolated OMD was significantly higher in tardive patients (p<0.05). Limb stereotypies, akathisia, and respiratory dyskinesia were seen only in the tardive OMD. Frequency of oro-facial-lingual stereotypy was significantly higher in the tardive than the idiopathic group (75.0% v 31.5%, p<0.0001). The peak effect of BTX was similar in both groups.
Oro-facial-lingual stereotypies were significantly more frequent in the tardive than the idiopathic group. Presence of stereotypic movements in the limbs, akathisia, and respiratory dyskinesias in patients with OMD strongly suggests prior neuroleptic exposure. Dystonia in tardive OMD is more likely to be restricted to the oromandibular region, whereas in patients with idiopathic OMD, there is often coexistent cervical dystonia. BTX is equally effective in both groups of patients.
大多数迟发性肌张力障碍患者起病局限于颅颈区域。由于其与特发性颅肌张力障碍(一种常见的肌张力障碍形式)相似,常带来诊断难题。比较迟发性与特发性口下颌肌张力障碍(OMD)患者的临床特征及对肉毒毒素(BTX)注射的反应。
研究运动障碍门诊中符合迟发性或特发性OMD纳入标准的患者。比较两组患者的临床变量及对BTX的反应。在迟发性组中,我们还比较了有口面部-舌部刻板动作的患者与无此症状患者之间的临床变量。
研究了24例迟发性OMD患者和92例特发性OMD患者。人口统计学特征无差异。大多数为女性,症状持续时间超过8年。抗精神病药物暴露的平均时长为7.1(标准差7.9)年。下颌闭合是OMD最常见的亚型(迟发性=41.7%,特发性=51.1%)。特发性患者更易合并颈部肌张力障碍(p<0.05),而迟发性患者孤立性OMD显著更多(p<0.05)。肢体刻板动作、静坐不能和呼吸运动障碍仅见于迟发性OMD。迟发性组口面部-舌部刻板动作的发生率显著高于特发性组(75.0%对31.5%,p<0.0001)。两组BTX的峰值效应相似。
迟发性组口面部-舌部刻板动作明显比特发性组更常见。OMD患者出现肢体刻板动作、静坐不能和呼吸运动障碍强烈提示既往有抗精神病药物暴露史。迟发性OMD的肌张力障碍更可能局限于口下颌区域,而特发性OMD患者常合并颈部肌张力障碍。BTX对两组患者同样有效。