Cutsforth-Gregory Jeremy K, Ahlskog J Eric, McKeon Andrew, Burnett Melinda S, Matsumoto Joseph Y, Hassan Anhar, Bower James H
Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Department of Neurology, Mayo Clinic, Rochester, MN, USA; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Parkinsonism Relat Disord. 2016 Jun;27:74-80. doi: 10.1016/j.parkreldis.2016.03.013. Epub 2016 Mar 18.
Runner's dystonia has previously been described in small series or case reports as a lower limb, task-specific dystonia. We have occasionally encountered this disorder and recognized the same phenomenon in non-runners regularly engaging in lower limb exercise. We wished to characterize the syndrome further, including outcomes, treatment, and the diagnostic usefulness of electrophysiology.
We conducted a retrospective review and follow-up survey of adults seen at Mayo Clinic (1996-2015) with task-specific dystonia arising after prolonged repetitive lower limb exercise. The findings were compared to all 21 previously reported cases of runner's dystonia.
We identified 20 patients with this condition, 13 runners and seven non-runner athletes. Median age at dystonia onset was in mid-adulthood. Correct diagnosis was delayed by a median of 3.5 years in runners and 1.6 years in non-runners, by which time more than one-third of patients had undergone unsuccessful invasive procedures. Most patients had dystonia onset in the distal lower limb. Dystonia was task-specific with exercise at onset but progressed to affect walking in most. Sensory tricks were reported in some. Surface EMG was consistent with task-specific dystonia in nine patients. Botulinum toxin, levodopa, clonazepam, trihexyphenidyl, and physical therapy provided modest benefit to some, but all patients remained substantially symptomatic at last follow up.
Repetitive exercise dystonia is task-specific, confined to the lower limb and occasionally trunk musculature. It tends to be treatment-refractory and limits ability to exercise. Diagnosis is typically delayed, and unnecessary surgical procedures are common. Surface EMG may aid the diagnosis.
此前,跑步者肌张力障碍在小规模系列研究或病例报告中被描述为一种下肢特定任务性肌张力障碍。我们偶尔会遇到这种疾病,并且在经常进行下肢锻炼的非跑步者中也发现了相同的现象。我们希望进一步描述该综合征,包括其结局、治疗方法以及电生理检查在诊断中的作用。
我们对梅奥诊所(1996 - 2015年)诊治的因长时间重复性下肢运动后出现特定任务性肌张力障碍的成年人进行了回顾性研究和随访调查。将研究结果与之前报道的21例跑步者肌张力障碍病例进行比较。
我们确定了20例患有这种疾病的患者,其中13例为跑步者,7例为非跑步运动员。肌张力障碍发病的中位年龄为中年。跑步者的正确诊断平均延迟3.5年,非跑步者平均延迟1.6年,到那时超过三分之一的患者已经接受了无效的侵入性治疗。大多数患者的肌张力障碍始于下肢远端。肌张力障碍在发病时与运动相关,具有特定任务性,但多数患者后来进展到影响行走。部分患者报告有感觉技巧现象。9例患者的表面肌电图与特定任务性肌张力障碍相符。肉毒毒素、左旋多巴、氯硝西泮、苯海索和物理治疗对部分患者有一定益处,但在最后一次随访时所有患者仍有明显症状。
重复性运动性肌张力障碍具有特定任务性,局限于下肢,偶尔累及躯干肌肉。它往往难以治疗,会限制运动能力。诊断通常会延迟,不必要的外科手术很常见。表面肌电图可能有助于诊断。