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Idiopathic Intracranial Hypertension: A Review of Nomenclature, Diagnostic Criteria and Management Strategies 特发性颅内高压:术语、诊断标准和治疗策略的综述
Pub Date : 2020-01-01 DOI: 10.17756/jnen.2020-071
Dhananjay Gupta, R. Pradeep, A. Mehta, M. Javali, P. T. Acharya, Srinivasa Rangasetty
Results and conclusion: Despite being a century old disease, the nomenclature and diagnostic criteria have undergone constant modifications. The most common symptoms are headache, visual disturbances and tinnitus. Treatment strategies include weight reduction, lifestyle modification, Acetazolamide, analgesics for headache, topiramate and surgical procedures like shunt diversion or optic nerve sheath fenestration.
结果与结论:尽管是一种有百年历史的疾病,但其命名和诊断标准经历了不断的修改。最常见的症状是头痛、视觉障碍和耳鸣。治疗策略包括减肥、改变生活方式、乙酰唑胺、头痛止痛药、托吡酯和外科手术,如分流术或视神经鞘开窗。
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引用次数: 0
Clinical, Laboratory and Neuroimaging Findings in Patients with Sarcoidosis Involving the CNS: Study of 29 Cases 29例结节病累及中枢神经系统的临床、实验室和神经影像学表现
Pub Date : 2020-01-01 DOI: 10.17756/jnen.2020-065
A. Mehta, J. Luo
Introduction: Sarcoidosis is a rare idiopathic systemic inflammatory disorder characterized by the formation of the non-caseating granulomas. Neurological complications involve approximately 5% of the patients with systemic sarcoidosis. Most literatures on neurosarcoidosis are anecdotal case reports. Studies of a series of cases of neurosarcoidosis are sparse. In this report, we studied clinical, laboratory and neuroimaging findings in patients with sarcoidosis involving the central nervous system (CNS). Methods: Clinical charts were retrospectively reviewed for the past 10 years to identify patients with a clinically conformed diagnosis of sarcoidosis, which was proven by a previously biopsied histological evaluation. Subjects with neurological presentation and clinically diagnosed neurosarcoidosis were collected. Subjects with identifiable etiologies causing a CNS structural lesion and/or dysfunction other than sarcoidosis, incomplete data, or sarcoidosis without nervous system complications were excluded. The collected data of clinical, laboratory and neuroimaging findings were analyzed. Results: Twenty-nine patients (age: 51.7 ± 9.0 years, range: 36 - 77, female / male = 21 / 8) were studied. Common clinical presentations were seizures (34.5%); Bell’s palsy (17.2%) with facial hypoesthesia (13.8%); limb weakness (13.8%) and/or numbness (6.9%); abducens nerve paresis (6.9%); hydrocephalus (6.9%), nystagmus (3.4%), and optical neuritis (3.4%). MRI showed abnormalities in discrete areas in the brain and spinal cord involving the parenchyma in different anatomic locations, leptomeninges and cranial nerves. Abnormal laboratory findings showed elevated ACE level in plasma and cerebrospinal fluid, impaired liver functions with reduced level of triglycerides, and elevated protein with decreased glucose and mild lymphocytosis in cerebrospinal fluid. Conclusion: Diagnosis of neurosarcoidosis remains a clinical challenge. Seizures were most frequently seen at presentation in patients with sarcoidosis involving the CNS. Laboratory studies of impaired liver function with reduced triglycerides, and CSF elevated levels of ACE and protein with decreased glucose and mild lymphocytosis may aid in differentiating neurosarcoidosis from other CNS inflammatory demyelinating disorders.
结节病是一种罕见的特发性全身性炎症性疾病,以非干酪化肉芽肿的形成为特征。神经系统并发症约占系统性结节病患者的5%。大多数关于神经结节病的文献都是轶事病例报告。对一系列神经结节病病例的研究很少。在本报告中,我们研究了结节病累及中枢神经系统(CNS)患者的临床、实验室和神经影像学表现。方法:回顾性回顾过去10年的临床图表,以确定临床符合结节病诊断的患者,这是由先前的活检组织学评估证实的。收集有神经学表现和临床诊断为神经结节病的受试者。除结节病、资料不完整或结节病无神经系统并发症外,有明确病因导致中枢神经系统结构病变和/或功能障碍的受试者被排除在外。对收集到的临床、实验室和神经影像学资料进行分析。结果:29例患者(年龄:51.7±9.0岁,范围:36 ~ 77岁,女/男= 21 / 8)。常见临床表现为癫痫发作(34.5%);贝尔氏麻痹(17.2%)伴面部感觉减退(13.8%);肢体无力(13.8%)和/或麻木(6.9%);展神经麻痹(6.9%);脑积水(6.9%),眼球震颤(3.4%),视神经炎(3.4%)。MRI显示脑和脊髓离散区异常,累及不同解剖部位的实质、脑膜和脑神经。异常实验室结果显示血浆和脑脊液中ACE水平升高,肝功能受损,甘油三酯水平降低,蛋白升高,葡萄糖降低,脑脊液中淋巴细胞轻度增多。结论:神经结节病的诊断仍是一个临床难题。发作最常见于结节病累及中枢神经系统的患者。肝功能受损,甘油三酯降低,脑脊液ACE和蛋白水平升高,葡萄糖降低,轻度淋巴细胞增多,可能有助于区分神经结节病与其他中枢神经系统炎症性脱髓鞘疾病。
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引用次数: 0
Global Virtual Conference on Alzheimer’s Disease and Dementia (GVCAD-2020) 全球阿尔茨海默病和痴呆症虚拟会议(GVCAD-2020)
Pub Date : 2020-01-01 DOI: 10.17756/jnen.2020-suppl2
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引用次数: 0
Online Meeting on Parkinson’s Disease (OMPD-2020) 帕金森病在线会议(OMPD-2020)
Pub Date : 2020-01-01 DOI: 10.17756/jnen.2020-suppl1
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引用次数: 0
Neurological Examination of Sheep (Ovis aries) with Unilateral and Bilateral Quinolinic Acid Lesions of the Striatum Assessed by Magnetic Resonance Imaging 磁共振成像对单侧和双侧纹状体喹啉酸病变羊的神经学检查的评价
Pub Date : 2019-08-06 DOI: 10.17756/jnen.2019-054
Adam B O'Connell, B. Sinnott, Timothy R. Kuchel, S. Perumal, Cara K Fraser, Kim M Hemsley, A. Jennifer Morton
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引用次数: 3
Neuromyelitis Optica as a Paraneoplastic Manifestation of Bronchogenic Carcinoma: A Case Report 视神经脊髓炎作为支气管源性癌的副肿瘤表现:1例报告
Pub Date : 2019-01-01 DOI: 10.17756/jnen.2019-058
W. Bahnasy, O. Ragab, Abdelmoneim Ahmed Nagy Eissa
Findings: This study reported a case of 65-year-old male patient with paraneoplastic NMOSD. The patient presented with quadriparesis due to acute cervical long segment myelitis not responsive to pulse steroid therapy; 18 months later he developed acute bilateral diminution of visual acuity due to bilateral optic neuritis with no response to either pulse steroid therapy or IVIG. Serological serum tests revealed that the patient was AQP–4–IgG positive, but after 22 months of the initial presentation, the patient showed widespread metastasis in bone and liver secondary to bronchogenic carcinoma.
结果:本研究报告1例65岁男性副肿瘤性NMOSD患者。患者因急性颈长段脊髓炎而出现四肢瘫,对脉冲类固醇治疗无反应;18个月后,由于双侧视神经炎,患者出现急性双侧视力下降,对脉冲类固醇治疗或IVIG均无反应。血清学血清检测显示患者AQP-4-IgG阳性,但在首次就诊22个月后,患者继发于支气管源性癌,出现骨和肝脏的广泛转移。
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引用次数: 2
Alzheimer’s Disease, is a Cure Possible? 阿尔茨海默病,有治愈的可能吗?
Pub Date : 2019-01-01 DOI: 10.17756/jnen.2019-050
B. Kakulas
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引用次数: 0
The Third Chinese American Neurological Association Annual Meeting 第三届中美神经学会年会
Pub Date : 2019-01-01 DOI: 10.17756/JNEN.2019-046
Kevin Xie, J. Luo
Published by United Scientific Group The 3rd Chinese American Neurological Association (CANA) Annual Meeting with CME credentials was successfully held in Houston, Texas on November 3, 2018. This CME meeting was combined with, and a part of, the Joint Annual Meeting of Alliance of North American Chinese Physicians (ANACP), CANA, and American Association of Chinese Rehabilitation Physicians (AACRP).
2018年11月3日,第三届中美神经病学协会(CANA) CME年会在美国德克萨斯州休斯顿成功召开。本次CME会议是北美中华医师联盟(ANACP)、CANA和美国中华康复医师协会(AACRP)联合年会的一部分。
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引用次数: 0
Idiopathic Focal Cerebritis Mimicking a Neoplasm 模拟肿瘤的特发性局灶性脑炎
Pub Date : 2019-01-01 DOI: 10.17756/jnen.2019-062
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引用次数: 1
Report on the 5th Neurological Disorders Summit (NDS-2019) 第五届神经系统疾病峰会(NDS-2019)报告
Pub Date : 2019-01-01 DOI: 10.17756/jnen.2019-055
J. Luo
5th Neurological Disorders Summit (NDS-2019) was held at Four Points by Sheraton, Los Angeles, CA, USA from July 18-20, 2019, organized by United Scientific Group, a nonprofit organization. This three-day conference had gathered 114 participants from 31 countries; had 64 oral presentations and 38 poster presentations on a wide variety of topics on Neurological Disorders and the related fields. Here are the highlights of some topics in the Summit.
第五届神经疾病峰会(NDS-2019)于2019年7月18日至20日在美国加利福尼亚州洛杉矶喜来登福点酒店举行,由非营利组织联合科学集团主办。这次为期三天的会议聚集了来自31个国家的114名与会者;有64个口头报告和38个海报报告,涉及神经疾病和相关领域的各种主题。以下是首脑会议部分议题的要点。
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引用次数: 0
期刊
Journal of neurology and experimental neuroscience
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