Marching neuropathy of the nervus digitalis plantaris proprii medialis halluci among military personnel

IF 3.2 4区 医学 Q2 CLINICAL NEUROLOGY
S. N. Bardakov, N. Khromov-Borisov, A. Belskikh, I. Litvinenko, A. V. Slobodya
{"title":"Marching neuropathy of the nervus digitalis plantaris proprii medialis halluci among military personnel","authors":"S. N. Bardakov, N. Khromov-Borisov, A. Belskikh, I. Litvinenko, A. V. Slobodya","doi":"10.17650/2222-8721-2023-13-2-64-71","DOIUrl":null,"url":null,"abstract":"Background. Marcher’s digitalgia paresthetica is a neuropathy of the medial plantar proper digital nerve (nervus digita lis plantaris proprii medialis halluci) and in some cases is accompanied by the formation of Joplin’s neuroma. Despite the general population rarity, marcher’s digitalgia paresthetica is significantly common among the special military contingent, athletes and tourists.Aim. To assess the prevalence of medial digital nerve neuropathy among military personnel and to identify possible factors contributing to its development.Materials and methods. The study involved 125 male servicemen of the Russian Federation, with an average age 37 (37–40) years. A neurological examination was performed with a detailed assessment of sensory disorders in the lower extremities, electroneuromyography and ultrasound examination of the leg nerves.Results. In 83 cases, or 66 (55–76) %, of digitalgia paresthetica were identified. Among them asymptomatic – 51 people, or 61 (47–74) %. In 27 cases – 33 (21–47) % – violation of sensitivity was observed on one side. The maximum area of violation of the sensitivity of the innervation of the medial‑plantar surface of the big toes was determined in 57 cases – 68 (55–80) %. At the same time, in 14 (6–25) % of the examined, the distal part of the second toe was additionally involved.Conclusion. In our study, the hypothesis about the influence of the type of footwear, the average daily duration of wearing and the frequency of its forced removal on the likelihood of developing paresthetic digitalgia was not confirmed. It is important that doctors are informed about the possible development of this neuropathy and its benign course.","PeriodicalId":16536,"journal":{"name":"Journal of neuromuscular diseases","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2023-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of neuromuscular diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.17650/2222-8721-2023-13-2-64-71","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background. Marcher’s digitalgia paresthetica is a neuropathy of the medial plantar proper digital nerve (nervus digita lis plantaris proprii medialis halluci) and in some cases is accompanied by the formation of Joplin’s neuroma. Despite the general population rarity, marcher’s digitalgia paresthetica is significantly common among the special military contingent, athletes and tourists.Aim. To assess the prevalence of medial digital nerve neuropathy among military personnel and to identify possible factors contributing to its development.Materials and methods. The study involved 125 male servicemen of the Russian Federation, with an average age 37 (37–40) years. A neurological examination was performed with a detailed assessment of sensory disorders in the lower extremities, electroneuromyography and ultrasound examination of the leg nerves.Results. In 83 cases, or 66 (55–76) %, of digitalgia paresthetica were identified. Among them asymptomatic – 51 people, or 61 (47–74) %. In 27 cases – 33 (21–47) % – violation of sensitivity was observed on one side. The maximum area of violation of the sensitivity of the innervation of the medial‑plantar surface of the big toes was determined in 57 cases – 68 (55–80) %. At the same time, in 14 (6–25) % of the examined, the distal part of the second toe was additionally involved.Conclusion. In our study, the hypothesis about the influence of the type of footwear, the average daily duration of wearing and the frequency of its forced removal on the likelihood of developing paresthetic digitalgia was not confirmed. It is important that doctors are informed about the possible development of this neuropathy and its benign course.
军人跖地黄固有内侧神经的行进神经病
背景。Marcher 's指感异常是指内侧趾固有神经(指跖固有内侧幻觉神经)的神经病变,在某些情况下伴有乔普林神经瘤的形成。尽管在一般人群中很少见,但游行者的数字感觉异常在特殊的军事特遣队、运动员和游客中非常普遍。评估军事人员内侧指神经病变的患病率,并确定可能导致其发展的因素。材料和方法。这项研究涉及125名俄罗斯联邦男性军人,平均年龄37岁(37 - 40岁)。进行神经学检查,详细评估下肢感觉障碍,神经肌电图和腿部神经超声检查。在83例中,66例(55-76)%被确诊为数字感觉异常。其中无症状者51例,占61(47-74)%。在27例(33(21-47)%)病例中,一侧观察到敏感性破坏。57例(68(55-80)%)测定了大趾内侧足底面神经支配敏感性的最大侵犯面积。同时,在14(6-25)%的检查中,第二趾远端部分额外受累。在我们的研究中,关于鞋类类型、平均每日穿着时间和强制脱鞋频率对发生数字感觉异常的可能性的影响的假设尚未得到证实。重要的是,医生被告知这种神经病变的可能发展及其良性进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信