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一名患有精神病性双相抑郁、紧张症和脑裂畸形的患者出现严重的丙咪嗪诱发肌阵挛。

Severe imipramine-induced myoclonus in a patient with psychotic bipolar depression, catatonia, and schizencephaly.

作者信息

Black K J, Kilzieh N

机构信息

Department of Psychiatry, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Ann Clin Psychiatry. 1994 Mar;6(1):45-9. doi: 10.3109/10401239409148839.

Abstract

Mild myoclonus is reasonably common with various cyclic antidepressants. However, antidepressants rarely cause severe myoclonus, and no risk or predisposing factors have been reported in the literature. We report a case of exceptionally severe myoclonus developing at therapeutic doses and modest serum levels of imipramine. The patient went on to experience dystonia and catatonia. Both of these were in typical settings (after haloperidol and with psychotic bipolar depression, respectively) and responded to typical treatment. On further investigation, the patient was found to have left-sided schizencephaly and a corresponding history of very mild developmental delay. We suggest that the onset of one movement disorder after drug therapy (eg, myoclonus) may predict the development of other movement disorders (e.g., catatonia). We further propose that severe tricyclic-induced myoclonus should prompt the physician to rule out a coexisting structural lesion of the central nervous system.

摘要

轻度肌阵挛在各种环类抗抑郁药使用中较为常见。然而,抗抑郁药很少引起严重肌阵挛,且文献中未报道过相关风险或易感因素。我们报告一例在治疗剂量和中等血清丙咪嗪水平时发生的异常严重肌阵挛病例。该患者继而出现肌张力障碍和紧张症。这两种情况均在典型情境下发生(分别在使用氟哌啶醇后和患有精神病性双相抑郁症时),并对典型治疗有反应。进一步检查发现,该患者患有左侧脑裂畸形且有非常轻微的发育迟缓病史。我们认为药物治疗后一种运动障碍(如肌阵挛)的发作可能预示着其他运动障碍(如紧张症)的发生。我们进一步提出,严重的三环类药物诱发的肌阵挛应促使医生排除中枢神经系统并存的结构性病变。

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