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一名纹状体黑质变性患者的早期运动波动

Early Motor Fluctuations in a Patient with Striatonigral Degeneration.

作者信息

Yoshii Fumihito, Moriya Yusuke, Ohnuki Tomohide, Takahashi Wakoh, Ryo Masafuchi

机构信息

Department of Neurology, Tokai University Oiso Hospital, Oiso, Japan.

出版信息

Case Rep Neurol. 2016 Dec 13;8(3):243-250. doi: 10.1159/000453254. eCollection 2016 Sep-Dec.

Abstract

We report a 44-year-old female with striatonigral degeneration (SND) who showed wearing-off oscillations after 4 months of levodopa treatment. The patient presented with asymmetric left-side dominant rigidity, and levodopa was effective at first. However, she began to show wearing-off oscillations of motor symptoms, which gradually worsened thereafter. Fluid-attenuated inversion recovery sequence magnetic resonance imaging (MRI) showed linear lateral putamen hyperintensities, and positron emission tomography (PET) studies using F-fluorodopa (FD) and C-N-methylspiperon (NMSP) showed a marked decrease of radioactivity in the right putamen, especially in the posterior putamen. The results of MRI and 2 PET studies with FD and NMSP were well consistent with the diagnosis of SND.

摘要

我们报告了一名44岁患有纹状体黑质变性(SND)的女性,她在左旋多巴治疗4个月后出现剂末波动。患者表现为以左侧为主的不对称性强直,左旋多巴起初有效。然而,她开始出现运动症状的剂末波动,此后逐渐加重。液体衰减反转恢复序列磁共振成像(MRI)显示壳核外侧呈线性高信号,使用F-氟多巴(FD)和C-N-甲基螺哌隆(NMSP)的正电子发射断层扫描(PET)研究显示右侧壳核放射性明显降低,尤其是壳核后部。MRI以及FD和NMSP的两项PET研究结果与SND的诊断高度一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb60/5216213/6245f0fa3fee/crn-0008-0243-g01.jpg

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