• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

起病时表现为髓鞘少突胶质细胞糖蛋白阳性视神经炎伪装的假性脑瘤。

Myelin oligodendrocyte glycoprotein-positive optic neuritis masquerading as pseudotumor cerebri at presentation.

机构信息

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Neuro-Immunology Service, Department of Neurology, Rabin Medical Center, Petah Tikva, Israel.

出版信息

J Neurol. 2018 Sep;265(9):1985-1988. doi: 10.1007/s00415-018-8956-y. Epub 2018 Jun 25.

DOI:10.1007/s00415-018-8956-y
PMID:29938337
Abstract

Optic neuritis (ON) is a common clinical manifestation in myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease. Other clinical manifestations include acute demyelinating encephalomyelitis, transverse myelitis and neuromyelitis optica spectrum disorders. Uncommon presentations of MOG-positive disease have recently been reported. ON in MOG-positive disease commonly involves the anterior portion of both optic nerves, leading to bilateral disc swelling. During the early stages of ON, in the setting of bilateral disc swelling and pain, patients may initially be suspected as pseudotumor cerebri (PTC). In this study, we report five cases presenting early in the course of MOG-IgG-related ON, which were misdiagnosed as PTC in the emergency department. MOG-IgG-positive ON requires timely treatment to prevent RNFL and vision loss secondary to the high relapse rate associated with these antibodies. Our aim is to increase the awareness of the unique findings of MOG-IgG-positive ON, which may initially mimic PTC, thereby delaying treatment.

摘要

视神经炎(ON)是髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病的常见临床表现。其他临床表现包括急性脱髓鞘性脑脊髓炎、横贯性脊髓炎和视神经脊髓炎谱系疾病。最近报道了 MOG 阳性疾病的不常见表现。MOG 阳性疾病中的 ON 常累及双侧视神经前部,导致双侧视盘肿胀。在 ON 的早期阶段,在双侧视盘肿胀和疼痛的情况下,患者最初可能被怀疑为假性脑瘤(PTC)。在本研究中,我们报告了 5 例在 MOG-IgG 相关性 ON 早期就诊的病例,这些病例在急诊科被误诊为 PTC。MOG-IgG 阳性 ON 需要及时治疗,以防止由于这些抗体相关的高复发率导致的 RNFL 和视力丧失。我们的目的是提高对 MOG-IgG 阳性 ON 的独特表现的认识,这些表现最初可能类似于 PTC,从而延迟治疗。

相似文献

1
Myelin oligodendrocyte glycoprotein-positive optic neuritis masquerading as pseudotumor cerebri at presentation.起病时表现为髓鞘少突胶质细胞糖蛋白阳性视神经炎伪装的假性脑瘤。
J Neurol. 2018 Sep;265(9):1985-1988. doi: 10.1007/s00415-018-8956-y. Epub 2018 Jun 25.
2
Clinical phenotype, radiological features, and treatment of myelin oligodendrocyte glycoprotein-immunoglobulin G (MOG-IgG) optic neuritis.髓鞘少突胶质细胞糖蛋白免疫球蛋白 G(MOG-IgG)视神经炎的临床表型、影像学特征和治疗。
Curr Opin Neurol. 2020 Feb;33(1):47-54. doi: 10.1097/WCO.0000000000000766.
3
Prevalence of Myelin Oligodendrocyte Glycoprotein and Aquaporin-4-IgG in Patients in the Optic Neuritis Treatment Trial.视神经炎治疗试验中患者的髓鞘少突胶质细胞糖蛋白和水通道蛋白4-IgG的患病率
JAMA Ophthalmol. 2018 Apr 1;136(4):419-422. doi: 10.1001/jamaophthalmol.2017.6757.
4
Myelin Oligodendrocyte Glycoprotein-IgG-positive Recurrent Bilateral Optic Papillitis with Serous Retinal Detachment.伴有浆液性视网膜脱离的髓鞘少突胶质细胞糖蛋白IgG阳性复发性双侧视神经乳头炎
Intern Med. 2018 Nov 15;57(22):3307-3312. doi: 10.2169/internalmedicine.9840-17. Epub 2018 May 18.
5
Aquaporin-4 and Myelin Oligodendrocyte Glycoprotein Autoantibody Status Predict Outcome of Recurrent Optic Neuritis.水通道蛋白-4 和髓鞘少突胶质细胞糖蛋白自身抗体状态预测复发性视神经炎的结局。
Ophthalmology. 2018 Oct;125(10):1628-1637. doi: 10.1016/j.ophtha.2018.03.041. Epub 2018 Apr 30.
6
Myelin Oligodendrocyte Glycoprotein Antibody-Positive Optic Neuritis: Clinical Characteristics, Radiologic Clues, and Outcome.髓鞘少突胶质细胞糖蛋白抗体阳性视神经炎:临床特征、放射学线索和结局。
Am J Ophthalmol. 2018 Nov;195:8-15. doi: 10.1016/j.ajo.2018.07.020. Epub 2018 Jul 26.
7
Atypical Anti-MOG syndrome with aseptic meningoencephalitis and pseudotumor cerebri-like presentations.抗 MOG 抗体综合征伴无菌性脑膜脑炎和类似颅内压增高表现
Mult Scler Relat Disord. 2019 Jan;27:30-33. doi: 10.1016/j.msard.2018.10.003. Epub 2018 Oct 3.
8
Clinical presentation of optic neuritis with autoantibodies anti-myelin oligodendrocyte glycoprotein.伴有抗髓鞘少突胶质细胞糖蛋白自身抗体的视神经炎的临床表现
Eur J Ophthalmol. 2019 Mar;29(2):257-261. doi: 10.1177/1120672118784797. Epub 2018 Jul 4.
9
Myelin oligodendrocyte glycoprotein-IgG-associated optic neuritis.髓鞘少突胶质细胞糖蛋白-IgG 相关视神经炎。
Curr Opin Ophthalmol. 2018 Nov;29(6):508-513. doi: 10.1097/ICU.0000000000000520.
10
Chronic relapsing inflammatory optic neuropathy (CRION): a manifestation of myelin oligodendrocyte glycoprotein antibodies.慢性复发性炎症性视神经病变(CRION):髓鞘少突胶质细胞糖蛋白抗体的一种表现。
J Neuroinflammation. 2018 Oct 31;15(1):302. doi: 10.1186/s12974-018-1335-x.

引用本文的文献

1
Bilateral optic neuritis in a patient with idiopathic intracranial hypertension: a case report.特发性颅内高压患者双侧视神经炎:一例报告
BMC Ophthalmol. 2025 Jul 16;25(1):414. doi: 10.1186/s12886-025-04233-2.
2
Isolated Intracranial Hypertensions as Onset of Myelin Oligodendrocyte Glycoprotein Antibody Disease.孤立性颅内高压作为髓鞘少突胶质细胞糖蛋白抗体病的首发表现。
J Clin Med. 2024 Jul 30;13(15):4468. doi: 10.3390/jcm13154468.
3
MOG antibody-associated optic neuritis.MOG 抗体相关性视神经炎。

本文引用的文献

1
Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease.髓鞘少突胶质细胞糖蛋白 IgG 疾病与水通道蛋白 4 IgG 疾病相关的癫痫发作和脑炎。
JAMA Neurol. 2018 Jan 1;75(1):65-71. doi: 10.1001/jamaneurol.2017.3196.
2
MOG antibody-related disorders: common features and uncommon presentations.MOG 抗体相关疾病:常见特征和不常见表现。
J Neurol. 2017 Sep;264(9):1945-1955. doi: 10.1007/s00415-017-8583-z. Epub 2017 Aug 2.
3
MOG antibody-positive, benign, unilateral, cerebral cortical encephalitis with epilepsy.
Eye (Lond). 2024 Aug;38(12):2289-2301. doi: 10.1038/s41433-024-03108-y. Epub 2024 May 23.
4
Myelin oligodendrocyte glycoprotein (MOG) associated optic neuritis in a patient with idiopathic intracranial hypertension (IIH) and compressive optic neuropathy case report.特发性颅内高压(IIH)合并压迫性视神经病变患者的髓鞘少突胶质细胞糖蛋白(MOG)相关性视神经炎病例报告。
BMC Ophthalmol. 2024 Feb 13;24(1):61. doi: 10.1186/s12886-023-03280-x.
5
Increased Intracranial Pressure in Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.小儿髓鞘少突胶质细胞糖蛋白抗体相关性疾病的颅内压增高。
Neurol Neuroimmunol Neuroinflamm. 2023 Nov 2;11(1). doi: 10.1212/NXI.0000000000200174. Print 2024 Jan.
6
Perplexing Initial Presentations of MOGAD in Two Children: Intracranial Hypertension and New-Onset Seizure.两名儿童MOGAD的复杂初始表现:颅内高压和新发癫痫。
Neurohospitalist. 2023 Oct;13(4):438-444. doi: 10.1177/19418744231192159. Epub 2023 Jul 25.
7
Pediatric myelin oligodendrocyte glycoprotein antibody associated disease-Asymmetric papilledema and elevated ICP are two of the chameleons: A case report.儿童髓鞘少突胶质细胞糖蛋白抗体相关性疾病-不对称性视盘水肿和颅内压升高是两个变色龙:病例报告。
Medicine (Baltimore). 2023 Feb 22;102(8):e32986. doi: 10.1097/MD.0000000000032986.
8
Obesity is associated with myelin oligodendrocyte glycoprotein antibody-associated disease in acute optic neuritis.肥胖与急性视神经炎中髓鞘少突胶质细胞糖蛋白抗体相关疾病有关。
Sci Rep. 2022 Dec 9;12(1):21312. doi: 10.1038/s41598-022-21592-8.
9
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Presenting as Intracranial Hypertension: A Case Report.髓鞘少突胶质细胞糖蛋白抗体相关性疾病表现为颅内压增高:病例报告。
Neurol Neuroimmunol Neuroinflamm. 2022 Oct 19;9(6). doi: 10.1212/NXI.0000000000200020. Print 2022 Nov.
10
Anti-MOG associated disease with intracranial hypertension after COVID-19 vaccination.新冠疫苗接种后出现颅内高压的抗髓鞘少突胶质细胞糖蛋白相关疾病
J Neurol. 2022 Oct;269(10):5647-5650. doi: 10.1007/s00415-022-11130-x. Epub 2022 Apr 23.
伴有癫痫发作的髓鞘少突胶质细胞糖蛋白(MOG)抗体阳性、良性、单侧大脑皮质脑炎
Neurol Neuroimmunol Neuroinflamm. 2017 Jan 16;4(2):e322. doi: 10.1212/NXI.0000000000000322. eCollection 2017 Mar.
4
MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 4: Afferent visual system damage after optic neuritis in MOG-IgG-seropositive versus AQP4-IgG-seropositive patients.视神经脊髓炎及相关疾病中的髓鞘少突胶质细胞糖蛋白免疫球蛋白G:50例患者的多中心研究。第4部分:髓鞘少突胶质细胞糖蛋白免疫球蛋白G血清阳性与水通道蛋白4免疫球蛋白G血清阳性患者视神经炎后传入视觉系统损伤
J Neuroinflammation. 2016 Nov 1;13(1):282. doi: 10.1186/s12974-016-0720-6.
5
MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 2: Epidemiology, clinical presentation, radiological and laboratory features, treatment responses, and long-term outcome.视神经脊髓炎及相关疾病中的髓鞘少突胶质细胞糖蛋白免疫球蛋白G:50例患者的多中心研究。第2部分:流行病学、临床表现、影像学和实验室特征、治疗反应及长期预后
J Neuroinflammation. 2016 Sep 27;13(1):280. doi: 10.1186/s12974-016-0718-0.
6
Anti-MOG antibody: The history, clinical phenotype, and pathogenicity of a serum biomarker for demyelination.抗髓鞘少突胶质细胞糖蛋白抗体:一种脱髓鞘疾病的血清生物标志物的历史、临床表型和致病性。
Autoimmun Rev. 2016 Apr;15(4):307-24. doi: 10.1016/j.autrev.2015.12.004. Epub 2015 Dec 17.
7
Anti-MOG antibodies are frequently associated with steroid-sensitive recurrent optic neuritis.抗髓鞘少突胶质细胞糖蛋白(MOG)抗体常与类固醇敏感的复发性视神经炎相关。
Neurol Neuroimmunol Neuroinflamm. 2015 Jul 2;2(4):e131. doi: 10.1212/NXI.0000000000000131. eCollection 2015 Aug.
8
Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis.伴有髓鞘少突胶质细胞糖蛋白抗体、水通道蛋白4抗体的视神经炎与多发性硬化症的影像学鉴别
Mult Scler. 2016 Apr;22(4):470-82. doi: 10.1177/1352458515593406. Epub 2015 Jul 10.
9
Histopathology and clinical course of MOG-antibody-associated encephalomyelitis.MOG 抗体相关性脑脊髓炎的组织病理学和临床病程。
Ann Clin Transl Neurol. 2015 Mar;2(3):295-301. doi: 10.1002/acn3.164. Epub 2015 Jan 14.
10
Does MOG Ig-positive AQP4-seronegative opticospinal inflammatory disease justify a diagnosis of NMO spectrum disorder?MOG 抗体阳性、AQP4 抗体阴性的视神经脊髓炎谱系疾病是否需要诊断为 NMOSD?
Neurol Neuroimmunol Neuroinflamm. 2015 Jan 22;2(1):e62. doi: 10.1212/NXI.0000000000000062. eCollection 2015 Feb.