Djaldetti R, Mosberg-Galili R, Sroka H, Merims D, Melamed E
Department of Neurology, Rabin Medical Center, Petah Tiqva, Israel.
Mov Disord. 1999 May;14(3):443-7. doi: 10.1002/1531-8257(199905)14:3<443::aid-mds1009>3.0.co;2-g.
Camptocormia is characterized by severe forward flexion of the thoracolumbar spine which increases while walking and disappears in the recumbent position. We describe for the first time eight patients with presumed idiopathic Parkinson's disease (mean age 66+/-5 yrs; mean symptom duration 13.1+/-5.1 yrs) who developed camptocormia. This impressive abnormal posture emerged 4-14 years from disease onset, and in some patients stooped posture was the prominent symptom at diagnosis. There was no clear correlation between camptocormia and levodopa treatment. In some patients the camptocormic posture improved, and in others it was unchanged or even aggravated following levodopa administration. Three patients reported worsening of this symptom during "off" periods and also with fatigue. The pathogenesis of this phenomenon is unknown but might represent either a rare type of dystonia or an extreme form of rigidity.
camptocormia的特征是胸腰椎严重向前屈曲,行走时加重,卧位时消失。我们首次描述了8例疑似特发性帕金森病患者(平均年龄66±5岁;平均症状持续时间13.1±5.1年)出现了camptocormia。这种令人印象深刻的异常姿势在疾病发作后4至14年出现,在一些患者中,弯腰姿势是诊断时的突出症状。camptocormia与左旋多巴治疗之间没有明显的相关性。在一些患者中,camptocormic姿势有所改善,而在另一些患者中,左旋多巴给药后姿势没有改变甚至加重。3例患者报告在“关”期以及疲劳时这种症状会加重。这种现象的发病机制尚不清楚,但可能代表一种罕见的肌张力障碍类型或一种极端形式的强直。