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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.

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。

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