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真性红细胞增多症一例罕见病例中的绝对难治性抑郁症和混合性运动障碍。

Absolutely therapy-resistant depression and mixed movement disorder in an unusual case of polycythemia vera.

作者信息

Bauer M

机构信息

Department of Psychiatry, Free University of Berlin, Germany.

出版信息

Pharmacopsychiatry. 1995 Mar;28(2):66-8. doi: 10.1055/s-2007-979592.

Abstract

This report presents a 64-year-old female patient with unusual psychiatric and neurological complications in polycythemia vera. Six years after onset of the hematologic disorder the patient succumbed to an absolutely therapy-resistant depression, from which she has been suffering for the past four years--intensive and broad--spectrum drug and electroconvulsive treatment has failed to ameliorate the condition. In addition, the patient has developed a mixed movement disorder with rhythmical movements, mainly affecting the trunk, akathisia, hyperventilation, and pleurothotonus ("Pisasyndrome"). The paper discusses a possible link between hypoxic cerebral damage, caused by hyperviscosity of the blood due to polycythemia vera, and the therapy resistance of the depression. The case confirms that organic factors may cause therapy resistance in depressive disorders.

摘要

本报告介绍了一位64岁的女性真性红细胞增多症患者,其出现了不寻常的精神和神经并发症。血液系统疾病发病6年后,患者死于一种完全抗治疗的抑郁症,她在过去四年中一直饱受此病折磨——强化和广谱药物治疗以及电休克治疗均未能改善病情。此外,患者还出现了一种混合性运动障碍,伴有节律性运动,主要影响躯干,还有静坐不能、换气过度和角弓反张(“皮萨综合征”)。本文讨论了真性红细胞增多症导致的血液高粘滞度引起的缺氧性脑损伤与抑郁症治疗抵抗之间可能存在的联系。该病例证实了器质性因素可能导致抑郁症的治疗抵抗。

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