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特发性腰骶丛神经炎

Idiopathic lumbosacral plexitis.

作者信息

Imam Yahia, Deleu Dirk, Salem Khaled

机构信息

Department of Neurology (Medicine), Hamad Medical Corporation, P. O. Box 3050, Doha, Qatar.

Department of Radiology, Hamad Medical Corporation, P. O. Box 3050, Doha, Qatar.

出版信息

Qatar Med J. 2013 Nov 1;2012(2):85-7. doi: 10.5339/qmj.2012.2.20. eCollection 2012.

Abstract

Idiopathic lumbosacral plexitis (LSP) or non-diabetic lumbosacral radiculoplexus neuropathy (LRPN) is a rare monophasic immune-mediated disorder. The disease is characterized by multiple lumbosacral root and nerve involvement in the absence of trauma, mass lesion or elevated blood sugar. We report a 60-year-old man presenting with a 4-day history of acute-onset sharp left hip pain radiating down his leg associated with numbness over the lateral dorsum of his left foot. MRI of the lumbosacral plexus revealed gadolinium enhancement of mainly L5 on the left. A dramatic response to oral steroids was observed.

摘要

特发性腰骶丛神经炎(LSP)或非糖尿病性腰骶神经根丛神经病(LRPN)是一种罕见的单相免疫介导性疾病。该疾病的特征是在无创伤、占位性病变或血糖升高的情况下,腰骶部多个神经根和神经受累。我们报告一名60岁男性,有4天急性发作的左侧髋部剧痛病史,疼痛向下放射至腿部,并伴有左足背外侧麻木。腰骶丛的MRI显示左侧主要为L5有钆增强。观察到对口服类固醇有显著反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8072/3991040/cd3b818ac57e/qmj-2012-084-g001.jpg

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