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Dominant posterior-variant alien hand syndrome after acute left parietal infarction.

机译:急性左顶壁梗死后占优势的后变种外来手综合征。

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摘要

Alien hand syndrome (AHS) is a complex clinical disorder in which patients develop a sense of estrangement from, and loss of volitional control of, an affected limb and non-purposeful complex motor actions of the same limb. Several forms of AHS exist, including frontal, callosal, and posterior types with a series of different associated neuroanatomical lesions and clinical symptoms. Most commonly, the lesions associated with AHS occur in the frontal lobes and corpus callosum. Rarely, lesions in the parietal lobes may be associated with AHS, and most often occur within the non-dominant hemisphere. We describe a 57-year-old patient who developed symptoms of posterior AHS after an acute infarction in the left (presumably dominant) parietal lobe. A review of the different clinical features of AHS and the underlying mechanisms is also presented.
机译:外来手综合症(AHS)是一种复杂的临床疾病,患者会因患肢和同一肢的无目的复杂运动动作而产生疏离感,并失去对这些肢体的意志控制。存在几种形式的AHS,包括额叶,call部和后部类型,以及一系列不同的相关神经解剖学病变和临床症状。最常见的是,与AHS相关的病变发生在额叶和call体中。罕见的是,顶叶的病变可能与AHS相关,并且最常见于非优势半球内。我们描述了一名57岁的患者,该患者在左(可能是占优势的)顶叶急性梗死后出现了后AHS症状。还介绍了AHS的不同临床特征及其潜在机制的综述。

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