Marked asymmetry of putaminal pathology in an MSA-P patient with Pisa syndrome

被引：15

作者：

Hozumi, I

Piao, YS

Inuzuka, T

Matsuyama, Z

Yamada, Y

Hara, A

Hirose, T

Tsuchiya, K

Takahashi, H

机构：

[1] Gifu Univ, Sch Med, Dept Neurol & Geriatr, Gifu 5008705, Japan

[2] Gifu Univ, Sch Med, Dept Pathol, Gifu 5008705, Japan

[3] Gifu Univ, Sch Med, Dept Internal Med 2, Gifu 5008705, Japan

[4] Niigata Univ, Brain Res Inst, Dept Pathol, Niigata, Japan

来源：

MOVEMENT DISORDERS | 2004年 / 19卷 / 04期

关键词：

striatonigral degeneration; multiple system atrophy; axial dystonia;

D O I：

10.1002/mds.10668

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

We report on an autopsy case of a 62-year-old Japanese woman with a 2.5-year history of axial dystonia. She presented with a form of axial dystonia reminiscent of Pisa syndrome. The pathophysiological mechanism underlying forms of axial dystonia remains to be elucidated. We report here the histopathological findings of a multiple system atrophy of parkinsonian predominance (MSA-P) patient with Pisa syndrome. (C) 2004 Movement Disorder Society.

引用

页码：470 / 472

页数：3

共 11 条

[1]

Boesch SM, 2002, J NEUROL NEUROSUR PS, V72, P300, DOI 10.1136/jnnp.72.3.300

[2] Pisa syndrome in a patient with multiple system atrophy [J].