Nonpainful Trigeminal Neuropathy Associated with a Solitary Pontine Lesion: A Case Series.

IF 2.1 4区 医学 Q3 CLINICAL NEUROLOGY European Neurology Pub Date : 2023-01-01 DOI:10.1159/000528470
Hüseyin Nezih Özdemir, Neşe Çelebisoy
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Abstract

A solitary pontine lesion (SPL) is a single brainstem lesion on the trigeminal nerve pathway without any other central nervous system lesion. This research aimed to investigate the demographic and clinical features of nonpainful TNO patients with SPL and identify the most frequently affected anatomical areas using lesion mapping techniques. Demographic and clinical features were retrospectively reviewed from the patients' charts. Brain lesions were mapped using MRIcroGL software. The study included 6 patients (three females and three males) with an SPL. The median age of the patients was 57 (range: 46-68) years. Cranial MRI displayed lesions in the dorsolateral pons and the cerebellar peduncle. The lesion mapping revealed that the lesions were on the trigeminal nerve pathway. SPL is an uncommon cause of TNO. Nonpainful SPL patients have demographic, clinical, and radiological features similar to those of painful SPL patients. The lesion mapping showed that the same brainstem areas are affected in painful and nonpainful SPL patients.

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非疼痛性三叉神经病变与孤立脑桥病变:一个病例系列。
孤立脑桥病变(SPL)是三叉神经通路上的单一脑干病变,没有任何其他中枢神经系统病变。本研究旨在探讨非疼痛性TNO伴SPL患者的人口学和临床特征,并利用病变作图技术确定最常受影响的解剖区域。从患者的病历中回顾了人口统计学和临床特征。使用MRIcroGL软件绘制脑病变图。本研究包括6例SPL患者(3女3男)。患者中位年龄为57岁(范围:46-68岁)。头颅MRI显示脑桥背外侧及小脑蒂病变。病变图显示病变位于三叉神经通路。SPL是一种罕见的TNO病因。非疼痛性SPL患者具有与疼痛性SPL患者相似的人口学、临床和放射学特征。病变映射显示,疼痛性和非疼痛性SPL患者的脑干区域受到相同的影响。
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来源期刊
European Neurology
European Neurology 医学-临床神经学
CiteScore
4.40
自引率
4.20%
发文量
51
审稿时长
4-8 weeks
期刊介绍: ''European Neurology'' publishes original papers, reviews and letters to the editor. Papers presented in this journal cover clinical aspects of diseases of the nervous system and muscles, as well as their neuropathological, biochemical, and electrophysiological basis. New diagnostic probes, pharmacological and surgical treatments are evaluated from clinical evidence and basic investigative studies. The journal also features original works and reviews on the history of neurology.
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