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进行性核上性麻痹和夏伊-德雷格综合征的磁共振成像

MR imaging in progressive supranuclear palsy and Shy-Drager syndrome.

作者信息

Savoiardo M, Strada L, Girotti F, D'Incerti L, Sberna M, Soliveri P, Balzarini L

机构信息

Department of Neuroradiology, Istituto Nazionale Neurologico C. Besta, Milano, Italy.

出版信息

J Comput Assist Tomogr. 1989 Jul-Aug;13(4):555-60. doi: 10.1097/00004728-198907000-00001.

Abstract

Previous reports have suggested that putaminal hypointensity in T2-weighted images at high field strength (1.5 T) magnetic resonance (MR) is a common finding in atypical parkinsonian syndromes, including progressive supranuclear palsy (PSP) and Shy-Drager syndrome (SDS). We have reviewed nine patients with PSP and five with SDS, selected on strict clinical criteria. Only in one PSP patient was abnormal signal intensity (putaminal hypointensity more marked than pallidal) found. However, hypointensity was often marked in the substantia nigra and occasionally in the superior colliculi. Focal midbrain atrophy, involving particularly the upper part of the quadrigeminal plate, was obvious in five cases. In general there was no uniformity of findings and MR appears unable to consistently support the clinical diagnosis of PSP. In SDS patients the findings were more uniform, with hypointensity in the putamen, superior or equal to that of the pallidum. At low or intermediate field strength, there was absence of magnetic susceptibility effect in the putamen, which appeared hyperintense. This was probably because of increased water content due to gliosis and/or cell loss. The constancy of the MR findings in our SDS series suggests a supportive diagnostic role for MR imaging.

摘要

先前的报告表明,在高场强(1.5T)磁共振(MR)成像的T2加权像中,壳核低信号是不典型帕金森综合征(包括进行性核上性麻痹(PSP)和Shy-Drager综合征(SDS))中的常见表现。我们依据严格的临床标准,回顾了9例PSP患者和5例SDS患者。仅在1例PSP患者中发现了异常信号强度(壳核低信号比苍白球更明显)。然而,黑质低信号常常较为明显,上丘偶尔也会出现低信号。5例患者中可见明显的中脑局灶性萎缩,尤其累及四叠体板上部。总体而言,各项发现并不一致,MR似乎无法始终支持PSP的临床诊断。在SDS患者中,表现更为一致,壳核呈低信号,强度高于或等同于苍白球。在低场强或中场强时,壳核不存在磁敏感效应,呈高信号。这可能是由于胶质增生和/或细胞丢失导致含水量增加所致。我们的SDS系列中MR表现的一致性表明MR成像具有辅助诊断作用。

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