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7例脑血管病继发格斯特曼综合征的临床分析

[Clinical analysis of 7 patients with Gerstmann syndrome secondary to cerebral vascular disease].

作者信息

Zhou Xiang-qin, He Rui, Liu Zhi, Wang Chang-qing

机构信息

Department of Neurology, PUMC Hospital, CAMS, PUMC, Beijing 100730, China.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2002 Oct;24(5):510-1.

Abstract

OBJECTIVE

To analyze clinical features of patients with Gerstmann syndrome (GS).

METHODS

We retrospectively analysed the clinical manifestations of 7 patients (6 men and 1 woman) with GS secondary to cerebral vascular diseases and reviewed the literatures.

RESULTS

The age ranged from 51 to 70 years with a mean of 70 years. They all had sudden onset and the tetrad of GS-finger agnosia, left-right disorientation, agraphia and acalculia, 3 patients accompanied by incomplete aphasia, 3 by anomic aphasia, 2 by alexia and 1 by constructional apraxia. Cranial computed tomographic scan showed low-density focus of the left parietal lobe in 6 cases and high-density focus of the left parietal lobe in 1 case.

CONCLUSION

GS has the high value in localization and the lesion is mainly localized to angular gyrus of the dominant hemisphere.

摘要

目的

分析格斯特曼综合征(GS)患者的临床特征。

方法

回顾性分析7例(6男1女)脑血管病继发GS患者的临床表现,并复习相关文献。

结果

年龄51~70岁,平均70岁。均急性起病,具备GS四联征——手指失认、左右定向障碍、失写和失算,3例伴有不完全性失语,3例伴有命名性失语,2例伴有失读,1例伴有结构性失用。头颅计算机断层扫描显示6例左侧顶叶低密度灶,1例左侧顶叶高密度灶。

结论

GS具有较高的定位价值,病变主要定位于优势半球角回。

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