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视神经胶质瘤的临床病理学研究 被引量:2
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作者 周海林 陈荣家 《临床眼科杂志》 2003年第2期104-106,T001,共4页
目的 观察视神经胶质瘤的临床病理特征。方法 回顾性分析 10例视神经胶质瘤的临床和病理学检查资料。结果 经病理学检查证实的 10例视神经胶质瘤都是星形胶质细胞瘤 ,均无恶性。但在幼儿和年长的病例中则表现瘤细胞生长活跃 ,侵及视... 目的 观察视神经胶质瘤的临床病理特征。方法 回顾性分析 10例视神经胶质瘤的临床和病理学检查资料。结果 经病理学检查证实的 10例视神经胶质瘤都是星形胶质细胞瘤 ,均无恶性。但在幼儿和年长的病例中则表现瘤细胞生长活跃 ,侵及视神经鞘膜 (2例 )。结论 视神经胶质瘤是危害少年儿童视神经的良性肿瘤 。 展开更多
关键词 临床病理学 视神经胶质瘤 视神经鞘膜 漏诊 误诊 星形胶质细胞瘤
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视神经胶质瘤的临床研究进展 被引量:5
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作者 郭辉 常祥平 梁冶矢 《肿瘤防治杂志》 2005年第13期1030-1034,共5页
视神经胶质瘤(optic pathwayglioma,OPG)是一种自然病程多变的罕见肿瘤,以儿童多发。OPG与神经纤维瘤病1型(neurofibromatosis type1,NF-1)的关系密切,其中并发NF-1的以前路OPG多见,多侵犯视神经与视交叉,发病年龄较小,常表现为良性自... 视神经胶质瘤(optic pathwayglioma,OPG)是一种自然病程多变的罕见肿瘤,以儿童多发。OPG与神经纤维瘤病1型(neurofibromatosis type1,NF-1)的关系密切,其中并发NF-1的以前路OPG多见,多侵犯视神经与视交叉,发病年龄较小,常表现为良性自限性肿瘤,症状以视觉损害为主,预后较好;而不并发NF-1的OPG常侵犯视交叉及下丘脑,发病年龄较大,且更具侵袭性,症状除视觉损害外还可表现为内分泌异常,预后相对较差。OPG的病理多为低级别的毛细胞型星形胶质细胞瘤,恶性OPG极为罕见。CT和MRI等影像学检查是诊断和随访OPG的重要手段。对无进展的OPG患者一般只需定期进行眼科及影像学检查随访,进展性OPG可采用手术、放疗、化疗或联合治疗以提高无进展生存率,但关于各种治疗方法的疗效、不良反应和预后对比缺乏大宗病例研究结果,目前尚无公认的最佳方案。 展开更多
关键词 视神经胶质瘤/病理学 眼肿瘤/病理学 治疗 预后 综述文献
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Neuroretinal dysfunction in patients affected by neurofibromatosis type 1
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作者 Antonietta Moramarco Luca Lucchino +6 位作者 Fabiana Mallone Michela Marcelli Ludovico Alisi Vincenzo Roberti Sandra Giustini Alessandro Lambiase Marcella Nebbioso 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2022年第5期773-779,共7页
AIM:To examine neuroretinal function by using the multifocal electroretinography(mf ERG)test in patients with neurofibromatosis type 1(NF1)without optic pathway gliomas(OPGs).METHODS:This study was conducted on 35 pat... AIM:To examine neuroretinal function by using the multifocal electroretinography(mf ERG)test in patients with neurofibromatosis type 1(NF1)without optic pathway gliomas(OPGs).METHODS:This study was conducted on 35 patients(35 eyes)with NF1 and 30 healthy subjects(30 eyes)for the control group.Each subject underwent a complete ophthalmological examination including spectral domainoptical coherence tomography(SD-OCT)and mf ERG.The 1.5-Tesla magnetic resonance imaging(MRI)scan of the brain was performed in NF1 patients to assess the presence of OPGs.All participants were recruited having a best corrected visual acuity(BCVA)of no less than 20/20 in each eye.The amplitude and implicit time of the P1 wave(first-order Kernel component)were evaluated on mf ERG.Data analysis was carried out in the two central degrees and in the four quadrants from two to 25 degrees of visual field.RESULTS:Statistically significant results were obtained for the P1 wave amplitudes in the 4 quadrants in NF1 patients compared to healthy controls,while the reduction was not significant in the 2 central degrees between the groups.A statistically significant difference was observed among the P1 wave amplitudes as recorded in the 4 quadrants within the NF1 group,with lower amplitudes detected in the nasal quadrants.No differences in the implicit times were recorded in the 2 central degrees and in the 4 quadrants as compared between NF1 patients and controls.CONCLUSION:Impaired neuroretinal function in NF1 patients is expressed in a decreased amplitude of the P1-wave between 2 and 25 central retinal degrees on mf ERG.Altered intracellular signal transduction due to abnormal neurofibromin-mediated cyclic adenosine monophosphate(c AMP)generation,can be involved.The possible use of mf ERG as subclinical retinal damage indicator has a potential utility in clinical practice for the follow-up of NF1 patients. 展开更多
关键词 neurofibromatosis type 1 multifocal electroretinography neuroretinal function optic pathway gliomas NEUROFIBROMIN
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Pediatric neuro-ophthalmology:not simply neuro-ophthalmology for small adults
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作者 Stacy L.Pineles 《Annals of Eye Science》 2018年第1期92-107,共16页
Pediatric neuro-ophthalmology is a subspecialty within neuro-ophthalmology.Pediatric neuro-ophthalmic diseases must be considered separate from their adult counterparts,due to the distinctive nature of the examination... Pediatric neuro-ophthalmology is a subspecialty within neuro-ophthalmology.Pediatric neuro-ophthalmic diseases must be considered separate from their adult counterparts,due to the distinctive nature of the examination,clinical presentations,and management choices.This manuscript will highlight four common pediatric neuro-ophthalmic disorders by describing common clinical presentations,recommended management,and highlighting recent developments.Diseases discussed include pediatric idiopathic intracranial hypertension(IIH),pseudopapilledema,optic neuritis(ON)and optic pathway gliomas(OPG).The demographics,diagnosis and management of common pediatric neuro-ophthalmic disease require a working knowledge of the current research presented herein.Special attention should be placed on the differences between pediatric and adult entities such that children can be appropriately diagnosed and treated. 展开更多
关键词 Pediatric neuro-ophthalmology optic neuritis(ON) optic disk drusen(ODD) pseudopapilledema idiopathic intracranial hypertension(IIH) optic pathway glioma
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不同年龄阶段儿童视路胶质瘤眼部首发症状特征分析
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作者 古丽娜·米吉提 施维 +4 位作者 李莉 余继锋 葛明 晏红改 彭春霞 《中华眼科杂志》 CAS CSCD 北大核心 2023年第5期376-380,共5页
目的探讨不同年龄阶段儿童视路胶质瘤眼部首发症状的特征。方法回顾性病例系列研究。收集2017年4月至2021年7月就诊于首都医科大学附属北京儿童医院眼科的16例视路胶质瘤患儿的临床资料。分析首发症状、眼部及神经系统临床表现、影像学... 目的探讨不同年龄阶段儿童视路胶质瘤眼部首发症状的特征。方法回顾性病例系列研究。收集2017年4月至2021年7月就诊于首都医科大学附属北京儿童医院眼科的16例视路胶质瘤患儿的临床资料。分析首发症状、眼部及神经系统临床表现、影像学及组织病理学特点,并比较年龄≤36个月的婴幼儿和年龄>36个月的大龄儿童患儿眼部首发症状的区别。结果16例患儿中男性9例,女性7例;发病年龄为15.0(6.3,56.5)个月,确诊年龄为48.0(11.3,78.0)个月。其中婴幼儿患儿11例,大龄儿童患儿5例。因眼部为首发症状而被确诊11例,其中婴幼儿患儿8例(5例表现为不规则的眼球震颤,2例表现为斜视,1例表现为不追视),大龄儿童患儿3例(2例表现为视力下降,1例表现为视盘水肿)。影像学表现以累及视交叉的视路胶质瘤占比最高,大龄儿童患儿和婴幼儿患儿分别为3例(3/5)和8例(8/11)。8例累及视交叉的视路胶质瘤患儿行手术治疗,其中5例组织病理结果提示毛细胞型星形细胞瘤。7例预后保存了有用视力;1例眼部出现震颤4年后,因出现头痛、呕吐等神经系统症状而行手术治疗,预后视力丧失伴有认知障碍。结论儿童视路胶质瘤多以眼部异常为首发症状,婴幼儿以眼球不规则震颤多见,大龄儿童以视力下降为主。 展开更多
关键词 视神经胶质瘤 视通路 眼震 病理性 儿童
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