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Ischemic strokes revealing neurosyphilis: Study of six (6) observations at the neurology Department of the University Hospital of Conakry 缺血性中风显示神经梅毒:在科纳克里大学医院神经内科进行的六(6)次观察研究
Q3 Neuroscience Pub Date : 2023-09-01 DOI: 10.1016/j.ensci.2023.100470
M.L. Touré , T.H. Baldé , M.S. Diallo , G. Carlos Othon , N. Camara , S.D. Barry , M.M. Konaté , F. Sakadi , E. Lamah , B. Diallo , M. Diakité , A. Sakho , D. Camara , S. Condé , H. Madandi , V. Millimono , A.K.T. Barry , M.T. Diallo , N. Traoré , F.D. Kassa , A. Cissé

Introduction

In sub-Saharan Africa (SSA), stroke is a major public health problem and the etiological aspects are poorly studied and documented because of under-medicalization; the syphilitic etiology is rarely mentioned.

Patients and methods

We performed a retrospective study of 472 patients hospitalized for ischemic stroke between 2016 and 2021 in the Neurology Department of the University Hospital of Conakry, confirmed by neuroradiological explorations (brain CT, MRI-Angio) and a biological workup including VDRL-TPHA serological reactions in blood and CSF.

Results

Syphilitic etiology was retained for six (6) patients (4 men and 2 women) with a mean age of 43 years (extremes 36 and 49 years). The clinical picture was dominated by carotid syndromes: superficial and deep sylvian syndrome, anterior cerebral artery syndrome and vertebro-basilar syndromes and one case of lacunar syndrome.

The diagnosis was based on the positivity of serological reactions (VDRL-TPHA) in blood and cerebrospinal fluid (CSF) and the presence of a predominantly lymphocytic hypercellularity and a hyperproteinorachy in the CSF in the absence of any other etiology.

Conclusion

These neurological vascular syndromes consecutive to a cerebral treponematous attack are often the result of a still poorly conducted management of primary and secondary syphilis in our country.

在撒哈拉以南非洲(SSA),中风是一个主要的公共卫生问题,由于医疗化程度低,其病因学方面的研究和记录很少;梅毒的病因很少被提及。患者和方法我们对2016年至2021年间在科纳克里大学医院神经内科住院的472例缺血性卒中患者进行了回顾性研究,并通过神经影像学检查(脑CT、mri血管造影)和包括血液和脑脊液中VDRL-TPHA血清学反应在内的生物学检查进行了证实。结果6例患者(男4例,女2例)保持梅毒病原学,平均年龄43岁(极端36岁和49岁)。临床表现以颈动脉综合征为主:浅、深颈动脉综合征、脑前动脉综合征、椎基底动脉综合征和1例腔隙综合征。诊断是基于血液和脑脊液(CSF)的血清学反应(VDRL-TPHA)阳性,以及在没有任何其他病因的情况下,脑脊液中主要存在淋巴细胞性高细胞性和高蛋白血症。结论这些神经血管综合征并发脑密螺旋体病发作,往往是由于我国对原发性和继发性梅毒管理不力所致。
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引用次数: 0
An adult progressive Langerhans cell histiocytosis with central nervous system involvement for 10 years: A case report 累及中枢神经系统10年的成人进行性朗格汉斯细胞组织细胞增多症1例报告
Q3 Neuroscience Pub Date : 2023-09-01 DOI: 10.1016/j.ensci.2023.100471
Hanxing Liu , Yumin Liu , Hong Cao , Yanping Liu

Introduction

Langerhans cell histiocytosis (LCH) is a rare disease that usually occurs in children <15 years of age. Adult-onset LCH is extremely rare. Previous published guidelines and studies mainly focused on pediatric patients. The rarity and also insufficient knowledge of LCH in adults, especially central neuvous system (CNS) involvement of LCH, often resulted in missed and delayed diagnosis.

Case presentation

A 35-year-old woman presented with cognitive impairment, anxietydepression, decreased eyesight, skin rash, hypernatremia, gonadal hormone deficiency and hypothyroidism. She had experienced menstrual disturbance and infertility since 10 years ago. MRI examination showed a mass lesion in the hypothalamic-pituitary region. Sighs of radiologic neurodegeneration were not found on brain MRI scans, however. Biopsy of skin rash confirmed the the diagnosis of multisystem LCH. BRAF V600E mutation was detected in the peripheral blood mononuclear cells. She accepted combination chemotherapy of vindesine and prednisone and accquired partial remission. The patient died of severe pneumonia during the second course of chemotherapy.

Conclusion

Given the complicated differential diagnoses of neuroendocrine disorders, it was essential to be aware of CNS involvement of LCH at first, especially in adults. BRAF V600E mutation may participated in disease progression.

朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的疾病,常见于15岁以下的儿童。成人发病的LCH极为罕见。以前发表的指南和研究主要集中在儿科患者。成人LCH的罕见性和对LCH的认识不足,特别是中枢神经系统(CNS)受累,经常导致漏诊和延误诊断。女性,35岁,主要表现为认知障碍、焦虑抑郁、视力下降、皮疹、高钠血症、性腺激素缺乏和甲状腺功能减退。从10年前开始,她就经历了月经紊乱和不孕。MRI检查显示下丘脑-垂体区肿块病变。然而,在脑部MRI扫描中未发现影像学神经退行性变的迹象。皮疹活检证实了多系统LCH的诊断。外周血单个核细胞检测到BRAF V600E突变。患者接受长春地西联合强的松化疗,病情部分缓解。病人在第二期化疗期间死于严重的肺炎。结论由于神经内分泌疾病的鉴别诊断复杂,LCH的早期诊断应注意中枢神经系统的受累,尤其是成人。BRAF V600E突变可能参与疾病进展。
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引用次数: 0
Headache advocacy 头痛的宣传
Q3 Neuroscience Pub Date : 2023-09-01 DOI: 10.1016/j.ensci.2023.100472
Wolfgang Grisold , David W. Dodick
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引用次数: 0
Secondary headaches - red and green flags and their significance for diagnostics 继发性头痛——红色和绿色标志及其诊断意义
Q3 Neuroscience Pub Date : 2023-09-01 DOI: 10.1016/j.ensci.2023.100473
Tissa Wijeratne , Chanith Wijeratne , Nadja Korajkic , Stefanie Bird , Carmela Sales , Franz Riederer

A small percentage of patients suffer from a secondary headache syndrome. It is imperative that clinicians are able to differentiate primary headache syndromes from secondary headache syndromes, as failure to do so significantly worsens morbidity and mortality. Recent advances in our understanding of pathobiological mechanisms offer useful information on these enigmatic disorders. We now understand that the causes of secondary headache syndromes can vary significantly – these may be infectious, inflammatory, vascular, traumatic or structural in origin.

A well-taken history and targeted physical examination coupled with appropriate investigations can enable these syndromes to be recognized consistently and thus allow their timely and appropriate treatment. Along with their epidemiology, some of their key characteristics shall thus be discussed in this review so as to aid the busy clinician at the bedside. Red flags including sudden onset, high pain intensity, pattern of change of a preexisting headache, focal neurological signs or seizure, systemic signs and precipitation by physical activity can guide the clinician to suspect a secondary headache. Importantly a preexisting headache is not an exclusion of a secondary headache – it might even be a predisposition in certain cases.

一小部分患者患有继发性头痛综合征。临床医生必须能够区分原发性头痛综合症和继发性头痛综合症,因为不能这样做会显著恶化发病率和死亡率。我们对病理生物学机制的理解的最新进展为这些神秘的疾病提供了有用的信息。我们现在了解到,继发性头痛综合征的病因可能有很大差异——这些病因可能是传染性的、炎症性的、血管性的、创伤性的或结构性的。良好的病史和有针对性的体检,再加上适当的调查,可以使这些综合征得到一致的识别,从而使其得到及时和适当的治疗。因此,在这篇综述中,除了他们的流行病学外,还将讨论他们的一些关键特征,以帮助床边忙碌的临床医生。危险信号包括突然发作、高疼痛强度、先前存在的头痛的变化模式、局灶性神经体征或癫痫发作、全身体征和身体活动引起的沉淀,可以引导临床医生怀疑是继发性头痛。重要的是,先前存在的头痛并不是继发性头痛的排除——在某些情况下,它甚至可能是一种易感性。
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引用次数: 1
Gender parity in high impact neurology journals 高影响力神经病学期刊中的性别平等
Q3 Neuroscience Pub Date : 2023-08-23 DOI: 10.1016/j.ensci.2023.100476
Dania Qaryouti , Omar Jibril , Floyd D. Silva , Priyanka Jain , Karthik Gangu , Abu Baker Sheikh

Background

Although female representation has been growing among physicians, women continue to be underrepresented in neurology, particularly regarding academic research in authorship and leadership. Analyzing recent trends in high-impact neurology journals highlights the underrepresentation of women and helps explore barriers to female representation in academic neurology.

Methods and results

Journal Citation Reports (JCR) for 2021 was used to screen neurology journals for selection. The first 15 journals with the highest impact factors (JIF) were included. 15,404 total articles in neurology were examined for gender distribution of editorial staff and authorship with the highest total citations from January 1st, 2018 to October 31st, 2021. Gender was classified using biographical information from public and personal media sources. Genderize.io was used in cases of ambiguity, predicting gender at probability of ≥95%. Our data demonstrated that these journals only had 13% female editor-in-chiefs and 35% female editorial staff. The data further demonstrated that females accounted for 39% of first authors and 26% for last authors. During the four years examined males continued to account for the vast majority of both first and last authors for publications accepted and journal editorial staff members.

Conclusion

Women are significantly under-represented in the field of neurological research in leadership positions as editor-in-chiefs, editorial board members as well as first or senior authors in top neurology medical journals. With continued underrepresentation of women occupying leading publishing roles, parity with men is still a work in progress. Additional work is needed to identify and address barriers to academic advancement for women physicians in academic neurology.

背景尽管女性在医生中的代表性一直在增加,但女性在神经病学领域的代表性仍然不足,尤其是在作者和领导力的学术研究方面。分析高影响力神经病学期刊的最新趋势,突出了女性代表性不足的问题,并有助于探索女性在学术神经病学中代表性的障碍。方法和结果2021年期刊引文报告(JCR)用于筛选神经病学期刊。收录了影响因子最高的前15种期刊。从2018年1月1日到2021年10月31日,对15404篇神经病学文章的编辑人员和作者的性别分布进行了检查,引用总数最高。根据公共和个人媒体提供的传记信息对性别进行分类。Genderize.io用于歧义情况,预测性别的概率≥95%。我们的数据显示,这些期刊只有13%的女性主编和35%的女性编辑人员。数据进一步表明,女性在第一作者中占39%,在最后作者中占26%。在接受检查的四年中,男性仍然占接受出版物的第一作者和最后作者以及期刊编辑人员的绝大多数。结论女性在神经病学研究领域担任主编、编委会成员以及顶级神经病学医学期刊的第一作者或高级作者等领导职务的人数明显不足。由于担任出版领导职务的妇女人数持续不足,与男子平等仍然是一项正在进行的工作。需要做更多的工作来确定和解决女性医生在学术神经病学领域学术进步的障碍。
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引用次数: 0
Wide symptom variability of cerebellar infarction and comparison with pons infarction 小脑梗死的广泛症状变异性及其与脑桥梗死的比较
Q3 Neuroscience Pub Date : 2023-06-01 DOI: 10.1016/j.ensci.2023.100459
Toralf Brüning, Tamara Beyrich, Mohamed Al-Khaled

Background and aim

Cerebellar infarction (CI) is a serious cerebrovascular disease that may present with non-focal neurological deficits, leading to delay of clinical recognition and treatment. The aim of this study is to investigate the variability of symptoms, diagnostic outcomes and early prognosis in patients with cerebellar infarction compared with pontine infarction (PI).

Methods

Between 2012 and 2014, a total of 79 patients (68 ± 14 years, female sex 42%, median NIHSS score: 5) with CI (43) and PI (36) were included and analyzed.

Results

CI patients were admitted to emergency department one hour earlier compared with patients with PI. The most common symptoms in CI were dysarthria (67%), impaired coordination (61%), limb weakness (54%), dizziness/vertigo (49%), gait and stance uncertainty (42%), nausea or/and vomiting (42%), nystagmus (37%), dysphagia (30%) and headache (26%). Nineteen patients (44%) had symptomatic stenosis and two patients had vertebral artery dissection on duplex sonography and MR angiography.

Four patients (9%) received a systemic intravenous thrombolysis with rt-PA and three patients received mechanical thrombectomy.

Three months after the event, five patients (12%) had died and 15 (40) had disability with mRS (3–5).

Conclusions

Cerebellar infarction occurs with a high variability of symptoms and should be considered when non-focal symptoms are present.

背景与目的小脑梗死是一种严重的脑血管疾病,可能表现为非局灶性神经功能缺损,导致临床认识和治疗的延误。本研究的目的是研究小脑梗死患者与桥脑梗死(PI)患者的症状、诊断结果和早期预后的可变性。方法在2012年至2014年间,共有79名患者(68±14岁,女性42%,中位NIHSS评分:5),CI(43)和PI(36)被纳入并分析。结果CI患者入院时间比PI患者提前1小时。CI最常见的症状是构音障碍(67%)、协调性受损(61%)、四肢无力(54%)、头晕/眩晕(49%)、步态和姿势不确定(42%)、恶心或/和呕吐(42%),眼球震颤(37%)、吞咽困难(30%)和头痛(26%)。19名患者(44%)出现症状性狭窄,2名患者在双功能超声和磁共振血管造影术中出现椎动脉夹层。4名患者(9%)接受了rt-PA全身静脉溶栓治疗,3名患者接受了机械血栓切除术。事件发生三个月后,5名患者(12%)死亡,15名(40)患有mRS残疾(3-5)。结论小脑梗死的症状变异性很高,当出现非局灶性症状时应予以考虑。
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引用次数: 0
Advocacy for patients with headache disorders 倡导头痛障碍患者
Q3 Neuroscience Pub Date : 2023-06-01 DOI: 10.1016/j.ensci.2023.100466
Riadh Gouider , Deborah Henscheid Lorenz , Audrey Craven , Wolfgang Grisold , David W. Dodick

Primary headache disorders are worldwide highly prevalent and burdensome and should be therefore considered as a global public health priority. However, too many patients with primary headache disorders still do not receive satisfying care. The most likely identified reasons for such a scenario - lack of public awareness, stigma, lack of trained professionals with inadequate healthcare systems and policies - are remediable. Despite the progresses that were made in headache advocacy, these efforts have not yielded substantial improvements in research funding or access to specialty care and even standards of care. The situation is more complex in Low and Middle Income Countries (LMICs) where headache advocacy is urgently needed given the magnitude of the difficulties that patients with primary headache disorders face in accessing care. The growing emergence of coordinated, collaborative, patient-centered advocacy efforts with improved patient-clinician partnership is an opportunity to enhance progress in advocacy for a satisfying life and optimal and equitable care for people with primary headache disorders. LMICs can benefit greatly from coordinating these efforts on a global scale. The recent organization of a training program on headache diagnosis and management for healthcare professionals in Africa is a concrete example.

原发性头痛疾病在世界范围内非常普遍,负担沉重,因此应被视为全球公共卫生的优先事项。然而,太多原发性头痛障碍患者仍然没有得到令人满意的护理。造成这种情况的最可能原因是缺乏公众意识、污名化、缺乏训练有素的专业人员、医疗系统和政策不足,这些都是可以补救的。尽管在头痛的宣传方面取得了进展,但这些努力并没有在研究资金或获得专业护理甚至护理标准方面产生实质性的改善。中低收入国家的情况更为复杂,考虑到原发性头痛障碍患者在获得护理方面面临的巨大困难,这些国家迫切需要头痛宣传。协调、协作、以患者为中心的宣传工作日益出现,患者与临床医生的合作关系得到改善,这是一个机会,可以在倡导原发性头痛障碍患者过上满意的生活和最佳、公平的护理方面取得进展。LMIC可以从全球范围内协调这些努力中受益匪浅。最近为非洲医疗保健专业人员组织的头痛诊断和管理培训项目就是一个具体的例子。
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引用次数: 0
Spinocerebellar Ataxia type 17 presenting with progressive myoclonic epilepsy 伴有进行性肌阵挛性癫痫的17型脊髓角性共济失调
Q3 Neuroscience Pub Date : 2023-06-01 DOI: 10.1016/j.ensci.2023.100463
Apisit Boongird, Pichet Termsarasab, Teeratorn Pulkes
{"title":"Spinocerebellar Ataxia type 17 presenting with progressive myoclonic epilepsy","authors":"Apisit Boongird,&nbsp;Pichet Termsarasab,&nbsp;Teeratorn Pulkes","doi":"10.1016/j.ensci.2023.100463","DOIUrl":"10.1016/j.ensci.2023.100463","url":null,"abstract":"","PeriodicalId":37974,"journal":{"name":"eNeurologicalSci","volume":"31 ","pages":"Article 100463"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/09/35/main.PMC10160684.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9798982","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Relapse of neuromyelitis optica spectrum disorder after BNT162b2 mRNA Covid-19 vaccination 接种BNT162b2mRNA新冠肺炎疫苗后视神经脊髓炎谱系障碍的复发
Q3 Neuroscience Pub Date : 2023-06-01 DOI: 10.1016/j.ensci.2023.100455
Qi Wang , Jin-Ju Kang , Yutong Bai , Sun-Young Oh
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引用次数: 0
Plasma exchange (PE) versus intravenous immunoglobulin (IVIG) for the treatment of Guillain-Barré syndrome (GBS) in patients with severe symptoms: A systematic review and meta-analysis 血浆置换(PE)与静脉注射免疫球蛋白(IVIG)治疗严重症状患者格林-巴利综合征(GBS)的系统综述和荟萃分析
Q3 Neuroscience Pub Date : 2023-06-01 DOI: 10.1016/j.ensci.2023.100468
Hany A. Zaki , Haris Iftikhar , Mavia Najam , Maarij Masood , Nood Dhafi R. Al-Marri , Mohamed Abdelgadir M. Elgassim , Mohamed Fayed , Eman E. Shaban

Background and purpose

Guillain- Barré syndrome (GBS) is a neuropathic condition that leads to the rapid development of impairments and is characterized by weakness and numbness or tingling sensation in the legs and arms and sometimes loss of movement and feeling in the legs, arms, upper body, and face. Currently, the cure for the disease is yet to be developed. However, treatment options such as intravenous immunoglobulin (IVIG) and plasma exchange (PE) have been used to minimize the symptoms and duration of the disease. Therefore, this systematic review and meta-analysis compared the efficacy of IVIG and PE in treating GBS patients with severe symptoms.

Methodology

Six electronic databases, including PubMed, Embase, Scopus, ScienceDirect, Medline, and Google scholar, were scoured for articles related and relevant to our research. Additionally, more studies were obtained through the reference lists of the studies retrieved from these electronic databases. Quality assessment and statistical data analysis were conducted using Review Manager software (RevMan 5.4.1).

Results

The search for relevant articles resulted in 3253 articles, of which only 20 were included for review in the current study. A sub-group analysis indicated no significant difference in the curative effect (Hughes score reduces by at least one score 4 weeks after GBS treatment; OR: 1.00; 95% CI: 0.66–1.52; p = 1.00 and Achieving grade 0 or 1 on Hughes scale; OR: 1.03; 95% CI: 0.27–3.94; p = 0.97). Similarly, the statistical showed that the difference in length of hospitalization and duration of mechanical ventilation was insignificant between the IVIG and PE group (Standard Mean Difference (SMD): -0.45; 95% CI: −0.92, 0.02; I2 = 91%; p = 0.06 and SMD: -0.54; 95% CI: −1.67, 0.59; I2 = 93%; p = 0.35, respectively). Moreover, the meta-analysis did not find any significant difference in the risk of GBS relapse (RR: 0.47; 95% CI: 0.20–1.14; p = 0.10) and risk of complications related to the treatment regimens (RR: 1.03; 95% CI: 0.71–1.48; p = 0.89). However, the statistical analysis of outcomes from 3 studies showed that the risk of discontinuation was significantly lower in the IVIG group than in the PE group (RR: 0.22; 95% CI: 0.06–0.88; p = 0.03).

Conclusion

Our study suggests that IVIG and PE have similar curative effects. Similarly, IVIG seems easier to use and thus can be preferred for treating GBS.

背景和目的格林-巴利综合征(GBS)是一种导致损伤快速发展的神经性疾病,其特征是腿部和手臂无力、麻木或刺痛感,有时腿部、手臂、上身和面部失去运动和感觉。目前,这种疾病的治疗方法尚待开发。然而,静脉注射免疫球蛋白(IVIG)和血浆置换(PE)等治疗方案已被用于尽量减少疾病的症状和持续时间。因此,本系统综述和荟萃分析比较了IVIG和PE治疗严重症状GBS患者的疗效。方法搜索了包括PubMed、Embase、Scopus、ScienceDirect、Medline和Google scholar在内的六个电子数据库,以查找与我们的研究相关的文章。此外,通过从这些电子数据库检索的研究参考文献列表,获得了更多的研究。使用Review Manager软件(RevMan 5.4.1)进行质量评估和统计数据分析。结果检索相关文章共3253篇,其中只有20篇纳入本研究进行审查。亚组分析表明,疗效无显著差异(GBS治疗4周后,Hughes评分至少降低一分;OR:1.00;95%CI:0.66–1.52;p=1.00;Hughes量表达到0或1级;OR:1.03;95%CI:0.27–3.94;p=0.97)。同样,统计显示IVIG组和PE组在住院时间和机械通气持续时间方面的差异不显著(SMD):-0.45;95%置信区间:-0.92,0.02;I2=91%;p=0.06,SMD:-0.54;95%置信区间:−1.67,0.59;I2=93%;p分别为0.35)。此外,荟萃分析未发现GBS复发风险(RR:0.47;95%CI:0.20-1.14;p=0.10)和与治疗方案相关的并发症风险(RR:1.03;95%CI:0.71–1.48;p=0.89)有任何显著差异。然而,对3项研究结果的统计分析显示,IVIG组的停药风险显著低于PE组(RR:0.22;95%CI:0.06–0.88;p=0.03)。结论我们的研究表明IVIG和PE具有相似的疗效。同样,IVIG似乎更容易使用,因此可以优先用于治疗GBS。
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引用次数: 0
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