遗传性脊髓小脑变性叠加紧张性木僵经电休克治疗后缓解。

Catatonic stupor superimposed on hereditary spinocerebellar degeneration resolved with electroconvulsive therapy.

作者信息

Suzuki Kazumasa, Itou Kae, Takano Takehisa, Harada Nobuhiko, Awata Shuichi, Matsuoka Hiroo

机构信息

Department of Psychiatry, Tohoku University Hospital, 1-1 Seiryo-machi, Sendai 980-8574, Japan.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2006 Aug 30;30(6):1179-81. doi: 10.1016/j.pnpbp.2006.04.026. Epub 2006 Jun 9.

DOI:10.1016/j.pnpbp.2006.04.026

PMID:16764981

Abstract

We report a 58-year-old woman with catatonic stupor superimposed on hereditary spinocerebellar degeneration (SCD) and psychotic depression. The catatonia and psychotic depression resolved with 11 sessions of electroconvulsive therapy (ECT). Early recognition of catatonia during the course of SCD is important for timely administration of ECT.

摘要

我们报告了一名58岁女性，患有遗传性脊髓小脑变性（SCD）合并紧张性木僵及精神病性抑郁。经11次电休克治疗（ECT）后，紧张症和精神病性抑郁得到缓解。在SCD病程中早期识别紧张症对于及时进行ECT治疗很重要。