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患有 Parry-Romberg 综合征相关面部疼痛患者的皮肤神经支配和三叉神经通路功能。

Cutaneous innervation and trigeminal pathway function in a patient with facial pain associated with Parry-Romberg syndrome.

机构信息

Department of Neurology and Psychiatry, Sapienza University, Viale Università 30, 00185, Rome, Italy.

出版信息

J Headache Pain. 2012 Aug;13(6):497-9. doi: 10.1007/s10194-012-0459-0. Epub 2012 May 24.

DOI:10.1007/s10194-012-0459-0
PMID:22623073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3464465/
Abstract

Parry-Romberg syndrome (PRS) is a rare condition manifesting with progressive hemifacial atrophy. Although reported PRS clinical disturbances include facial pain and recent studies raised the possibility that PRS-related pain is a neuropathic pain condition due to the trigeminal nerve damage, no studies have directly investigated cutaneous innervation and trigeminal pathway function in patients with this rare condition. In a 50-year-old woman presenting with a 10-year history of slowly progressive hemifacial atrophy and facial pain, we investigated large myelinated fibres with masticatory muscle electromyography and trigeminal reflexes, and tested small myelinated and unmyelinated fibres with laser-evoked potentials. We also investigated cutaneous innervation by measuring the intraepidermal nerve fibre (IENF) density after skin biopsy of the supraorbital regions. We found that neurophysiological data and IENF density came within normal ranges, with no differences between normal and affected side. Our study showing that the standard reference techniques for assessing cutaneous innervation and trigeminal pathway function disclosed no abnormalities in this patient with PRS suggest that this rare and disabling condition is not associated with trigeminal system damage. These findings indicate that in this patient PRS-related pain is not a neuropathic pain condition, rather it probably arises from the musculoskeletal abnormalities.

摘要

进行性半面萎缩症(PRS)是一种罕见的疾病,表现为进行性半侧面部萎缩。尽管报道的PRS 临床障碍包括面部疼痛,最近的研究提出 PRS 相关疼痛是由于三叉神经损伤引起的神经病理性疼痛状况的可能性,但尚无研究直接调查这种罕见疾病患者的皮肤神经支配和三叉神经通路功能。在一位 50 岁女性中,我们发现进行性半面萎缩和面部疼痛已有 10 年的病史,我们用咀嚼肌肌电图和三叉神经反射检查大的有髓纤维,并通过激光诱发电位测试小的有髓和无髓纤维。我们还通过测量眶上区域皮肤活检后的表皮内神经纤维(IENF)密度来研究皮肤神经支配。我们发现神经生理学数据和 IENF 密度均在正常范围内,正常侧和受累侧之间无差异。我们的研究表明,用于评估皮肤神经支配和三叉神经通路功能的标准参考技术并未发现该 PRS 患者存在异常,这表明这种罕见且使人丧失能力的疾病与三叉神经系统损伤无关。这些发现表明,在该患者中,PRS 相关的疼痛不是神经病理性疼痛状况,而是可能源于肌肉骨骼异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5717/3464465/ac578f1a2e01/10194_2012_459_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5717/3464465/a84614d9ecdd/10194_2012_459_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5717/3464465/ac578f1a2e01/10194_2012_459_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5717/3464465/a84614d9ecdd/10194_2012_459_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5717/3464465/ac578f1a2e01/10194_2012_459_Fig2_HTML.jpg

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