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单侧脑桥梗死后出现橄榄核肥大性变性伴双侧小脑中脚脑桥外侧髓鞘溶解症。

Hypertrophic olivary degeneration concomitant with bilateral middle cerebellar peduncles Wallerian degeneration following unilateral pontine infarction.

机构信息

Department of Neurology, The Affiliated Hospital of Jiujiang University, No.57 Xunyang East Rode, Xunyang District, Jiujiang, 332000, Jiangxi Province, China.

出版信息

BMC Neurol. 2020 Nov 7;20(1):409. doi: 10.1186/s12883-020-01984-x.

Abstract

BACKGROUND

Wallerian degeneration (WD) can occur in different projecting systems, such as corticospinal tract, dentate-rubro-olivary pathway, and corticopontocerebellar tract. However, the co-occurrence of hypertrophic olivary degeneration (HOD) and middle cerebellar peduncles (MCPs) degeneration secondary to unilateral pontine infarction in a single patient is extremely rare.

CASE PRESENTATION

A 71-year-old man presented with acute onset of dizzness, slurred speech, and right-sided weakness. On the next day, his previous neurologic deficits deteriorated. Brain magnetic resonance imaging (MRI) revealed acute ischemic stroke of the left pons. After treatment with thrombolysis, antiplatelets, and rehabilitation training, his speaking and motor function improved moderately. At the 3-month follow-up, the MRI showed hyperintensity in the left medulla oblongata and bilateral MCPs on T2-weighted and FLAIR images, suggesting HOD as well as MCPs degeneration.

CONCLUSIONS

It is of great importance for us to know the anatomic knowledge of dentate-rubro-olivary and corticopontocerebellar pathways.

摘要

背景

Wallerian 变性(WD)可发生于不同的投射系统,如皮质脊髓束、齿状核红核橄榄束和皮质脑桥小脑束。然而,单侧脑桥梗死患者同时出现肥大性橄榄变性(HOD)和中间脑桥小脑脚(MCPs)变性极为罕见。

病例介绍

一名 71 岁男性突发头晕、言语不清和右侧无力。次日,其先前的神经功能缺损恶化。脑磁共振成像(MRI)显示左侧脑桥急性缺血性卒中。溶栓、抗血小板和康复训练后,其言语和运动功能中度改善。3 个月随访时,MRI 显示左侧延髓和双侧 MCPs 在 T2 加权和 FLAIR 图像上呈高信号,提示 HOD 以及 MCPs 变性。

结论

了解齿状核红核橄榄束和皮质脑桥小脑束的解剖知识非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e8e/7648961/7e9fab07d861/12883_2020_1984_Fig1_HTML.jpg

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