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使用角膜共焦显微镜和皮肤活检对结节病和慢性疼痛患者的小纤维病理进行定量分析。

Quantification of small fiber pathology in patients with sarcoidosis and chronic pain using cornea confocal microscopy and skin biopsies.

作者信息

Oudejans Linda Cj, Niesters Marieke, Brines Michael, Dahan Albert, van Velzen Monique

机构信息

Department of Anesthesiology, Leiden University Medical Center, Leiden, the Netherlands.

Araim Pharmaceuticals, Inc., Tarrytown, NY, USA.

出版信息

J Pain Res. 2017 Aug 26;10:2057-2065. doi: 10.2147/JPR.S142683. eCollection 2017.

DOI:10.2147/JPR.S142683
PMID:28894389
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5584894/
Abstract

Small fiber pathology with concomitant chronic neuropathic pain is a common complication of sarcoidosis. The gold standard of diagnosis of small fiber neuropathy (SFN) is the quantification of small nerve fibers in skin biopsies in combination with patient history and psychophysical tests; a new technique is the quantification of small nerve fibers in the cornea using cornea confocal microscopy (CCM). Here, we studied small fiber morphology in sarcoidosis patients with neuropathic pain using skin biopsies, CCM, and quantitative sensory testing (QST). Our aim was to construct specific phenotypes of neuropathic pain in sarcoidosis. Fifty-eight patients with a confirmed diagnosis of sarcoidosis and with moderate-to-severe neuropathic pain were tested. Decreased intraepidermal nerve fiber density (IENFD) from skin biopsies was found in 28% of patients, and CCM abnormalities were observed in 45% of patients. There was no correlation between CCM and IENFD abnormalities. Eighty-three percent of patients had abnormal thermal detection thresholds, a sign of small fiber dysfunction. Based on the presence or absence of abnormalities in IENFD and CCM, four distinct phenotypes were identified with a distinct homogeneous pattern of somatosensory symptoms. We argue that these distinct phenotypes have a similar mechanistic construct with specific phenotype-specific treatment options. Additionally, our data suggest the presence of patients with length- and nonlength-dependent SFN within this population of sarcoidosis patients.

摘要

小纤维病变伴发慢性神经性疼痛是结节病的常见并发症。小纤维神经病变(SFN)诊断的金标准是结合患者病史和心理物理测试对皮肤活检中的小神经纤维进行定量;一种新技术是使用角膜共聚焦显微镜(CCM)对角膜中的小神经纤维进行定量。在此,我们使用皮肤活检、CCM和定量感觉测试(QST)研究了患有神经性疼痛的结节病患者的小纤维形态。我们的目的是构建结节病中神经性疼痛的特定表型。对58例确诊为结节病且患有中度至重度神经性疼痛的患者进行了测试。28%的患者皮肤活检显示表皮内神经纤维密度(IENFD)降低,45%的患者观察到CCM异常。CCM与IENFD异常之间无相关性。83%的患者热觉阈值异常,这是小纤维功能障碍的迹象。根据IENFD和CCM是否存在异常,确定了四种不同的表型,具有明显的体感症状同质模式。我们认为这些不同的表型具有相似的机制结构以及特定的表型特异性治疗方案。此外,我们的数据表明在这群结节病患者中存在长度依赖性和非长度依赖性SFN患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/4bed9b216900/jpr-10-2057Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/9c230297cd15/jpr-10-2057Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/29ae49712679/jpr-10-2057Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/d7f248763fbf/jpr-10-2057Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/185dedf22031/jpr-10-2057Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/4bed9b216900/jpr-10-2057Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/9c230297cd15/jpr-10-2057Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/29ae49712679/jpr-10-2057Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/d7f248763fbf/jpr-10-2057Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/185dedf22031/jpr-10-2057Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2585/5584894/4bed9b216900/jpr-10-2057Fig5.jpg

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