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痣样基底细胞癌综合征患者视觉通路的电生理研究

Electrophysiological Study of Visual Pathways in Nevoid Basal Cell Carcinoma Syndrome Patients.

作者信息

Moramarco Antonietta, Alisi Ludovico, Lambiase Alessandro, Giustini Sandra, Lucchino Luca, Miraglia Emanuele, Roberti Vincenzo, Nebbioso Marcella

机构信息

Department of Sense Organs, Faculty of Medicine and Odontology, Sapienza University of Rome, Rome, 00161, Italy.

Department of Dermatology, Sapienza University of Rome, Rome, 00185, Italy.

出版信息

Eye Brain. 2021 Mar 29;13:71-78. doi: 10.2147/EB.S281135. eCollection 2021.

Abstract

INTRODUCTION

Gorlin-Goltz syndrome (GGS) also known as nevoid basal cell carcinoma syndrome (NBCCS) is a complex rare genetic disorder characterized by a wide range of clinical and radiological manifestations. Ophthalmological alterations have always been reported, but no study on the eventual pattern visual evoked potentials (pVEPs) abnormalities has yet been published.

PURPOSE

The purpose of the study was to evaluate the functionality of the optic pathways in a group of NBCCS patients through pattern reversal VEPs, after a thorough exclusion of subjects with preexisting ocular and optic pathways pathologies.

METHODS

Nineteen NBCCS patients (31 eyes) and 20 healthy controls (40 eyes) have been recruited for this study. All subjects underwent an evaluation of the functionality of the optic pathways through pVEPs with small (120'), medium (60'), and large (15') check size stimulation.

RESULTS

NBCCS patients showed a statistically significant alteration in the transmission of the macular pathway function when compared to controls. PVEPs analysis confirmed a reduced amplitude and an increased latency of the P100 component, suggesting an involvement of the visual pathway even in the absence of ocular clinical manifestations.

CONCLUSION

Visual pathways may have been affected both by a subclinical myelination deficit, determined directly by the genetic alteration, as well as by neurological abnormalities typical of this syndrome. Further studies are warranted.

摘要

引言

戈林-戈尔茨综合征(GGS)也称为痣样基底细胞癌综合征(NBCCS),是一种复杂的罕见遗传性疾病,具有广泛的临床和放射学表现。一直有眼科改变的报道,但尚未发表关于最终模式视觉诱发电位(pVEP)异常的研究。

目的

本研究的目的是在彻底排除已有眼部和视路病变的受试者后,通过模式反转VEP评估一组NBCCS患者视路的功能。

方法

本研究招募了19名NBCCS患者(31只眼)和20名健康对照者(40只眼)。所有受试者均通过小(120')、中(60')和大(15')检查尺寸刺激的pVEP对视路功能进行评估。

结果

与对照组相比,NBCCS患者黄斑通路功能的传递在统计学上有显著改变。PVEPs分析证实P100成分的振幅降低和潜伏期延长,表明即使在没有眼部临床表现的情况下,视觉通路也受到了影响。

结论

视觉通路可能受到了直接由基因改变决定的亚临床髓鞘形成缺陷以及该综合征典型的神经学异常的影响。有必要进行进一步的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ec/8018356/648a2f66a41a/EB-13-71-g0001.jpg

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