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神经鞘瘤病中 C 纤维丧失可能是神经性疼痛的原因。

C-Fiber Loss as a Possible Cause of Neuropathic Pain in Schwannomatosis.

机构信息

Department of Neurology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Department of Neurology, Charité University Medicine, 10117 Berlin, Germany.

出版信息

Int J Mol Sci. 2020 May 18;21(10):3569. doi: 10.3390/ijms21103569.

DOI:10.3390/ijms21103569
PMID:32443592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7278954/
Abstract

Schwannomatosis is the third form of neurofibromatosis and characterized by the occurrence of multiple schwannomas. The most prominent symptom is chronic pain. We aimed to test whether pain in schwannomatosis might be caused by small-fiber neuropathy. Twenty patients with schwannomatosis underwent neurological examination and nerve conduction studies. Levels of pain perception as well as anxiety and depression were assessed by established questionnaires. Quantitative sensory testing (QST) and laser-evoked potentials (LEP) were performed on patients and controls. Whole-body magnetic resonance imaging (wbMRI) and magnetic resonance neurography (MRN) were performed to quantify tumors and fascicular nerve lesions; skin biopsies were performed to determine intra-epidermal nerve fiber density (IENFD). All patients suffered from chronic pain without further neurological deficits. The questionnaires indicated neuropathic symptoms with significant impact on quality of life. Peripheral nerve tumors were detected in all patients by wbMRI. MRN showed additional multiple fascicular nerve lesions in 16/18 patients. LEP showed significant faster latencies compared to normal controls. Finally, IENFD was significantly reduced in 13/14 patients. Our study therefore indicates the presence of small-fiber neuropathy, predominantly of unmyelinated C-fibers. Fascicular nerve lesions are characteristic disease features that are associated with faster LEP latencies and decreased IENFD. Together these methods may facilitate differential diagnosis of schwannomatosis.

摘要

神经鞘瘤病是神经纤维瘤病的第三种形式,其特征是多发性神经鞘瘤的发生。最突出的症状是慢性疼痛。我们旨在测试神经鞘瘤病患者的疼痛是否可能是由小纤维神经病引起的。20 名神经鞘瘤病患者接受了神经系统检查和神经传导研究。通过既定的问卷评估疼痛感知水平以及焦虑和抑郁程度。对患者和对照组进行定量感觉测试(QST)和激光诱发电位(LEP)。进行全身磁共振成像(wbMRI)和磁共振神经成像(MRN)以量化肿瘤和束状神经病变;进行皮肤活检以确定表皮内神经纤维密度(IENFD)。所有患者均患有慢性疼痛,无进一步的神经功能缺损。问卷表明存在有明显生活质量影响的神经病理性症状。wbMRI 在所有患者中均检测到周围神经肿瘤。MRN 在 16/18 名患者中显示出额外的多发性束状神经病变。LEP 与正常对照组相比潜伏期明显更快。最后,13/14 名患者的 IENFD 明显降低。因此,我们的研究表明存在小纤维神经病,主要是无髓鞘 C 纤维。束状神经病变是特征性疾病特征,与更快的 LEP 潜伏期和降低的 IENFD 相关。这些方法可以共同促进神经鞘瘤病的鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/3f9c67767cca/ijms-21-03569-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/9621ffedb58a/ijms-21-03569-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/8b035fc2d2d4/ijms-21-03569-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/9bf6f896579c/ijms-21-03569-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/3f9c67767cca/ijms-21-03569-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/9621ffedb58a/ijms-21-03569-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/8b035fc2d2d4/ijms-21-03569-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/9bf6f896579c/ijms-21-03569-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7278954/3f9c67767cca/ijms-21-03569-g004.jpg

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