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Fibroblasts:New players in the central nervous system? 被引量:1
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作者 Lihui Duan Xiang Yu 《Fundamental Research》 CAS CSCD 2024年第2期262-266,共5页
Fibroblasts are typically described as cells that produce extracellular matrix,contribute to the formation of connective tissue,and maintain the structural framework of tissues.Fibroblasts are the first cell type to b... Fibroblasts are typically described as cells that produce extracellular matrix,contribute to the formation of connective tissue,and maintain the structural framework of tissues.Fibroblasts are the first cell type to be transdifferentiated into inducible pluripotent stem cells(iPSCs),demonstrating their versatility and reprogrammability.Currently,there is relatively extensive characterization of the anatomical,molecular,and functional diversity of fibroblasts in different peripheral organs and tissues.With recent advances in single cell RNA sequencing,heterogeneity and diversity of fibroblasts in the central nervous system(CNS)have also begun to emerge.Based on their distinct anatomical locations in the meninges,perivascular space,and choroid plexus,as well as their molecular diversity,important roles for fibroblasts in the CNS have been proposed.Here,we draw inspirations from what is known about fibroblasts in peripheral tissues,in combination with their currently identified CNS locations and molecular characterizations,to propose potential functions of CNS fibroblasts in health and disease.Future studies,using a combination of technologies,will be needed to determine the bona fide in vivo functions of fibroblasts in the CNS. 展开更多
关键词 FIBROBLASTS central nervous system infection AGinG Neurodegenerative diseases inJURY
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Neurological complications of hematopoietic cell transplantation in children and adults 被引量:4
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作者 Adriana Octaviana Dulamea Ioana Gabriela Lupescu 《Neural Regeneration Research》 SCIE CAS CSCD 2018年第6期945-954,共10页
Hematopoietic cell transplantation(HCT) is widely performed for neoplastic and non-neoplastic diseases. HCT involves intravenous infusion of hematopoietic progenitor cells from human leukocyte antigen(HLA)-matched... Hematopoietic cell transplantation(HCT) is widely performed for neoplastic and non-neoplastic diseases. HCT involves intravenous infusion of hematopoietic progenitor cells from human leukocyte antigen(HLA)-matched donor(allogeneic) or from the patient(autologous). Before HCT, the patient is prepared with high dose chemotherapy and/or radiotherapy to destroy residual malignant cells and to reduce immunologic resistance. After HCT, chemotherapy is used to prevent graft rejection and graft versus host disease(Gv HD). Neurological complications are related to the type of HCT, underlying disease, toxicity of the conditioning regimens, immunosuppression caused by conditioning regimens, vascular complications generated by thrombocytopenia and/or coagulopathy, Gv HD and inappropriate immune response. In this review, neurological complications are presented according to time of onset after HCT:(1) early complications(in the first month)-related to harvesting of stem cells, during conditioning(drug toxicity, posterior reversible encephalopathy syndrome), related to pancytopenia,(2) intermediate phase complications(second to sixth month)-central nervous system infections caused by prolonged neutropenia and progressive multifocal leukoencephalopathy due to JC virus,(3) late phase complications(after sixth month)-neurological complications of Gv HD, second neoplasms and relapses of the original disease. 展开更多
关键词 neurological complications hematopoietic cell transplantation posterior reversible encephalopathy syndrome central nervous system infections progressive multifocal leukoencephalopathy graft versus host disease second neoplasm immune reconstitution inflammatory syndrome post-transplant acute limbic encephalitis drug reaction with eosinophiIia and systemic symptoms
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Endogenous Endophthalmitis as a Triggering Factor for Fatal Bacterial Meningitis Caused by Streptococcus pneumoniae: A Case Report
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作者 David Fernando Ortiz-Pérez Mario Enrique Montoya-Jaramillo +8 位作者 Juan Pablo de la Ossa Díaz Natalia Vanessa Benavides-Garzón Luis Augusto Martínez-Aguilera Luis Miguel Orozco-Pabón Santiago José González-Manzur Víctor Santiago Márquez-Camacho Miguel Gregorio Tordecilla-Castro Gustavo Alberto Gutiérrez Barros John Sebastián Osorio-Muñoz 《Journal of Biosciences and Medicines》 2024年第10期97-104,共8页
Endogenous endophthalmitis is a rare condition with a poor long-term visual prognosis and significant mortality, often associated with the hematogenous spread of intravitreal infections and subsequent disruption of th... Endogenous endophthalmitis is a rare condition with a poor long-term visual prognosis and significant mortality, often associated with the hematogenous spread of intravitreal infections and subsequent disruption of the blood-ocular barrier. Its anatomical proximity to the central nervous system (CNS) poses a high risk of infection dissemination, although cases documented in the literature are rare, and endogenous endophthalmitis is typically described as secondary to neuroinfections. We report the case of an 82-year-old female patient with a history of hypertension who presented with fever, decreased visual acuity, severe headache, chemosis, and conjunctival injection. Endogenous endophthalmitis was diagnosed, and antimicrobial treatment was initiated alongside surgical intervention by the ophthalmology service. However, the patient’s condition worsened neurologically, and Streptococcus pneumoniae was identified in cerebrospinal fluid cultures. Despite intensive medical treatment, the patient’s clinical course was poor, leading to death. 展开更多
关键词 central nervous system infections MENinGITIS infectious disease Medicine Endogenous Endophthalmitis
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Cauda equina arachnoiditis–a rare manifestation of West Nile virus neuroinvasive disease:A case report
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作者 Marija Santini Ivana Zupetic +11 位作者 Klaudija Viskovic Juraj Krznaric Marko Kutlesa Vladimir Krajinovic Vlatka Lovrakovic Polak Vladimir Savic Irena Tabain Ljubo Barbic Maja Bogdanic Vladimir Stevanovic Anna Mrzljak Tatjana Vilibic-Cavlek 《World Journal of Clinical Cases》 SCIE 2020年第17期3797-3803,共7页
BACKGROUND Data regarding the neuroradiology features of the West Nile virus neuroinvasive disease(WNV NID)is rather scarce.To contribute to the knowledge of the WNV NID,we present a patient with a combination of ence... BACKGROUND Data regarding the neuroradiology features of the West Nile virus neuroinvasive disease(WNV NID)is rather scarce.To contribute to the knowledge of the WNV NID,we present a patient with a combination of encephalitis and acute flaccid paresis,with cauda equina arachnoiditis as the main magnetic resonance(MR)finding.CASE SUMMARY A 72-year-old female patient was admitted due to fever,headache and gait instability.During the first several days she developed somnolence,aphasia,urinary incontinence,constipation,and asymmetric lower extremities weakness.Cerebrospinal fluid analysis indicated encephalitis.Native brain computed tomography and MR were unremarkable,while spinal MR demonstrated cauda equina enhancement without cord lesions.Virology testing revealed WNV IgM and IgG antibodies in serum and cerebrospinal fluid,which confirmed acute WNV NID.The treatment was supportive.After two months only a slight improvement was noticed but cognitive impairment,loss of sphincter control and asymmetric inferior extremities weakness remained.The patient died after a month on chronic rehabilitation.CONCLUSION Cauda equina arachnoiditis is a rare,but possible neuroradiological feature in acute flaccid paresis form of WNV NID. 展开更多
关键词 West Nile virus central nervous system infection Cauda equina Magnetic resonance Neuroinvasive disease Case report
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Long-term outcome of acute central nervous system infection in children 被引量:4
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作者 Tianming Chen Gang Liu 《Pediatric Investigation》 2018年第3期155-163,共9页
Importance:Central nervous system infection is a severe illness in children.Little is known about the long-term outcome in children with central nervous system infection of various etiologies.Objective:The aims of thi... Importance:Central nervous system infection is a severe illness in children.Little is known about the long-term outcome in children with central nervous system infection of various etiologies.Objective:The aims of this study were to investigate the long-term outcomes of childhood acute central nervous system infection and to examine possible prognostic factors.Methods:Of 172 children who were treated for acute central nervous system infection from January 2009 through December 2009,139 were eligible for follow-up evaluations.A structured interview was conducted with the parents 3.8-4.7 years after hospital discharge.The global outcome was determined in all patients using the Pediatric Version of the Glasgow Outcome Scale-Extended.Clinical features of the acute episode were retrieved from medical records.Results:The outcome was favorable in 109 of 139 patients (78%),38 (27%) were mildly impaired,six (4%) were moderately impaired,14 (10%) were severely impaired and two (1%) were in a vegetative state.There were eight deaths.The most frequent symptoms were difficulty concentrating (16%),epilepsy (12%),limb paralysis (12%),memory impairment (10%),speech disorders (9%),irritability (9%).Significant risk factors for epilepsy included the presence of recurrent seizures or status epilepticus,the existence of pure spikes in the electroencephalogram,brain parenchyma abnormalities on neuroimaging and herpes simplex virus encephalitis (HSVE).A multivariate analysis identified three factors that were independently associated with poor outcome:coma,brain parenchyma abnormalities on neuroimaging and HSVE.Interpretation:Most children with acute central nervous system infection experienced a favorable outcome 3.8-4.7 years after discharge from the hospital.Minor to severe disability persists in a high proportion of cases.Coma,brain parenchymal abnormalities on neuroimaging and HSVE may predict poor long-term outcome. 展开更多
关键词 central nervous system infection LONG-TERM OUTCOME PROGNOSIS children
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降钙素原、C反应蛋白及白细胞计数在儿童中枢神经系统感染性疾病诊断中的应用价值 被引量:19
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作者 林茂增 陈尔东 《中国实验诊断学》 2017年第4期610-613,共4页
目的探讨降钙素原(PCT)、C反应蛋白(CRP)及白细胞计数(WBC)在儿童中枢神经系统感染性疾病中的诊断价值。方法选取中枢神经系统感染患儿100例,根据感染致病菌不同分为化脓组和病毒组,每组各50例,观察两组患儿血清和脑脊液中白细胞计数、... 目的探讨降钙素原(PCT)、C反应蛋白(CRP)及白细胞计数(WBC)在儿童中枢神经系统感染性疾病中的诊断价值。方法选取中枢神经系统感染患儿100例,根据感染致病菌不同分为化脓组和病毒组,每组各50例,观察两组患儿血清和脑脊液中白细胞计数、C反应蛋白、降钙素原及乳酸脱氢酶(LHD)含量,同时观察比较两种检验标本阳性率。结果两组患儿入院时和恢复期脑脊液中CRP、PCT、LHD水平,明显低于同组血清中含量;化脓组患儿入院时和恢复期脑脊液中WBC水平,明显低于血清中水平,差异有统计学意义(P<0.05);化脓组患儿入院时和恢复期血清、脑脊液中WBC、CRP、PCT、LHD水平,均明显高于病毒组患儿水平,差异有统计学意义(P<0.05)。化脓组患儿入院时血清、脑脊液中WBC、CRP、PCT、LHD水平阳性率,均明显高于病毒组同样本阳性率,差异有统计学意义(P<0.05)。结论中枢神经系统感染性疾病患儿如血清CRP、PCT、LHD均为阳性,即可确诊为细菌感染,可避免腰穿,方便易行,值得推广应用。 展开更多
关键词 降钙素原 C反应蛋白 白细胞计数 乳酸脱氢酶 儿童中枢神经系统感染性疾病
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手足口病合并中枢神经系统损害54例临床分析 被引量:6
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作者 张燕君 白君 黄晓利 《中国急救医学》 CAS CSCD 北大核心 2010年第12期1090-1092,共3页
目的 分析手足口病合并中枢神经系统损害的典型临床表现,探讨危重症病例的早期识别、早期治疗的指征.方法 采用回顾性病例分析方法,对2010-05~2010-09在我院住院治疗的54例合并中枢神经系统损害的手足口病病例进行临床分析.结果 54例... 目的 分析手足口病合并中枢神经系统损害的典型临床表现,探讨危重症病例的早期识别、早期治疗的指征.方法 采用回顾性病例分析方法,对2010-05~2010-09在我院住院治疗的54例合并中枢神经系统损害的手足口病病例进行临床分析.结果 54例患儿平均年龄(2.7±1.1)岁,男:女为2.4∶ 1.均表现为发热、皮疹(占100%),伴有惊跳44例(81.5%),四肢抖动31例(57.4%),呕吐25例(占46.3%),精神差14例(占25.9%),烦躁5例(占9.3%),嗜睡5例(占9.3%),惊厥4例(7.4%),四肢弛缓性瘫痪2例(3.7%).血糖升高25例(占46.3%),外周血WBC升高26例(占48.1%).肠道病毒71型(EV71)检测阳性44例(占81.5%),柯萨奇A16型(CoxA16)检测阳性13例(占24.1%),二者混合感染3例(占9.3%).52例临床治愈(占96.3%),2例死亡(占3.7%).结论 EV71更易引起中枢神经系统合并症,四肢抖动及惊跳是危重症手足口病合并中枢神经系统损害的早期明显表现,尤其小于3岁儿童,在高热期出现四肢抖动、惊跳,应警惕合并中枢神经系统损害,早期诊断及治疗有助于提高治愈率. 展开更多
关键词 手足口病 中枢神经系统感染 儿童 危重症 肠道病毒71型
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儿童手足口病合并中枢神经系统感染的MRI表现(附36例分析) 被引量:5
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作者 聂磊 《医学影像学杂志》 2015年第1期31-33,共3页
目的探讨手足口病患儿合并中枢神经系统感染的MRI表现。方法回顾性分析本院36例手足口病患儿合并中枢神经系统感染的MRI表现特点。结果 MRI表现为脑干偏背侧片状等或稍长T1长T2信号7例,其中中脑受累2例,桥延交界区受累5例。MRI表现为脊... 目的探讨手足口病患儿合并中枢神经系统感染的MRI表现。方法回顾性分析本院36例手足口病患儿合并中枢神经系统感染的MRI表现特点。结果 MRI表现为脑干偏背侧片状等或稍长T1长T2信号7例,其中中脑受累2例,桥延交界区受累5例。MRI表现为脊髓前角等长T1长T2信号29例,其中颈段脊髓受累7例,上胸段受累1例,下胸段至腰骶段脊髓受累19例,累及多段脊髓3例;脊髓内双侧受累25例,单侧受累4例。结论 MRI能清晰显示手足口病患儿合并中枢神经系统感染的病变特点,是影像学首选检查方法,为临床诊断治疗、评价治疗效果提供了可靠依据。 展开更多
关键词 儿童 手足口病 中枢神经系统感染 磁共振成像
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