眼科文献摘要

Cindy Cline, K. Fray, Bruce A. Furr, L. Pendarvis, C. Pritchard, Nicholas Strauss, K. Arnoldi
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引用次数: 0

摘要

眼科文献汇编:Cindy Cline、Katherine Fray、Bruce Furr博士、Lauren Pendarvis、Cindy Pritchard、Nicholas Strauss、Kyle Arnoldi、ARMANGUE T、SABATER L、TORRES-VEGA E、MARTiNEZ HERNANDEZ E、ARINO H、PETITPEDROL M、PLANAGUMA J、BATALLER L、DALMAU J,GRAUS F:神经元细胞表面抗体时代视锁索肌阵挛综合征的临床和免疫学特征。JAMAN欧洲2016;肌阵挛综合征(OMS)是一种罕见的疾病,其特征是不自主、心律失常、多向扫视,伴有四肢和躯干肌阵挛性抽搐、小脑共济失调、震颤和脑病。在一项对114名成年OMS患者的回顾性队列研究中,作者报告了特发性OMS(I-OMS)和副肿瘤性OMS的临床和免疫学特征。45例(39%)有P-O~S,69例(61%)有I-OMS。P-OMS中最常见的相关肿瘤是年轻病例中的肺癌(42%)和乳腺癌(22%)以及卵巢畸胎瘤(18%)。I-OMS患者比P-OMS患者年轻(中位年龄,38岁vs 54岁;P<0.001),更经常出现前驱症状或活动性感染(33%vs 13%;P=0.02),脑病发生率较低(10%对29%;p=O.Oll,预后较好(84%对39%;p<0.001),复发率较少(7%对24%;p=0.04)。这些结果表明,年龄较大和脑病与p-OMS显著相关,是提示潜在肿瘤的临床线索。I-OMS患者对治疗反应更好,复发更少。P-OMS和I-OMS之间的临床差异表明,每个触发剂的疾病机制不同。他们得出结论,未来旨在确定OMS免疫机制的研究应侧重于不同于自身免疫性脑炎和细胞表面抗原的方法。Francesco Graus,医学博士,博士,神经病学服务,医院诊所,Villarroel 170,巴塞罗那08036,西班牙电子邮件:fgraus@clinic.catASLAM T,TAHIR H,PARRY N,MURRAY I,KWAK K,REYES R,SALLER M,CZANNER G,ASHWORTH J:使用游戏设计原理和平板电脑自动测量儿童眼科患者的视觉敏锐度。美国眼科杂志2016;170:223-227。本研究的目的是通过交互式计算机对儿童视力的移动评估来确定触摸屏游戏型视力评估的有效性(MAVERIC-J。该研究包括112名年龄在4岁至16岁之间的儿童。如果儿童无法使用该设备,则不包括在内。在包括的112名儿童中,95%能够完成测试©2017威斯康星大学系统董事会,《美国骨科杂志》,2017年第67卷,ISSN 0065-955X,E-ISSN 1553-4448
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstracts of the Ophthalmic Literature
s of the Ophthalmic Literature Compiled by: Cindy Cline, C.O. Katherine Fray, C.O. Bruce Furr, Ph.D., C.O. Lauren Pendarvis, C.O. Cindy Pritchard, C.O. Nicholas Strauss, C.O. Kyle Arnoldi, C.O. ARMANGUE T, SABATER L, TORRES-VEGA E, MARTiNEZ-HERNANDEZ E, ARINO H, PETITPEDROL M, PLANAGUMA J, BATALLER L, DALMAU J, GRAUS F: Clinical and immunological features of opsoclonus-myoclonus syndrome in the era of neuronal cell surface antibodies. JAMANeurol2016; 73:417-421. Opsoclonus-myoclonus syndrome (OMS) is a rare condition characterized by involuntary, arrhythmic, multidirectional saccades accompanied by myoclonic jerks in the limbs and trunk, cerebellar ataxia, tremor and encephalopathy. In a retrospective cohort study of 114 adult patients with OMS, the authors report the clinical and immunological features of idiopathic OMS (I-OMS) and paraneoplastic OMS
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