Monday K, Jankovic J
Department of Neurology, Baylor College of Medicine, Houston, TX 77030.
Neurology. 1993 Feb;43(2):349-52. doi: 10.1212/wnl.43.2.349.
We report 18 patients (13 women, 5 men; age range, 22 to 75 years; mean, 42.5), whom we ultimately diagnosed as having "psychogenic myoclonus." The myoclonus was present for an average of 36 months (range, 1 to 110), and it was segmental in 10, generalized in seven, and focal in one. Stress precipitated or exacerbated the myoclonic movements in 15 patients; 14 had a definite increase in myoclonic activity during periods of anxiety. A combination of the following findings helped to establish the psychogenic nature of the myoclonus: (1) clinical features incongruous with "organic" myoclonus, (2) evidence of underlying psychopathology, (3) an improvement with distraction in 14 and with placebo in nine, and (4) the presence of incongruous sensory loss or false weakness in five. Over half of all patients with adequate follow-up improved after gaining insight into the psychogenic mechanisms of their movement disorder. This study attempts to characterize psychogenic myoclonus, the most common psychogenic movement disorder in our movement disorders clinic, and provides a guide to its diagnosis and treatment.
我们报告了18例患者(13名女性,5名男性;年龄范围22至75岁,平均42.5岁),最终诊断为“心因性肌阵挛”。肌阵挛平均持续36个月(范围1至110个月),其中10例为节段性,7例为全身性,1例为局灶性。压力促使或加重了15例患者的肌阵挛动作;14例在焦虑期间肌阵挛活动明显增加。以下多种表现共同有助于确立肌阵挛的心因性本质:(1)临床特征与“器质性”肌阵挛不符;(2)存在潜在精神病理学证据;(3)14例通过分散注意力、9例通过安慰剂治疗后病情改善;(4)5例存在不符常理的感觉丧失或假性肌无力。在所有接受充分随访的患者中,超过半数在洞察其运动障碍的心因机制后病情改善。本研究旨在描述心因性肌阵挛(我们运动障碍门诊最常见的心因性运动障碍)的特征,并为其诊断和治疗提供指导。