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髓鞘少突胶质细胞糖蛋白抗体相关疾病中的颅内压升高

Increased Intracranial Pressure in Myelin-Oligodendrocyte Glycoprotein Antibody-Associated Disease.

作者信息

Rempe Torge, Elfasi Aisha, Alkabie Samir, Christy Alison, Rodriguez Elsa, Castrodad-Molina Rhaisa, Buchowicz Bryce, Cuascut Fernando X, Hutton George, Kinkel Revere, Graves Jennifer

机构信息

Department of Neurology, College of Medicine, University of Florida, Gainesville, FL.

Department of Neurology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Lenox Hill Hospital, New York, NY.

出版信息

Neurologist. 2025 Jan 1;30(1):17-22. doi: 10.1097/NRL.0000000000000577.

Abstract

OBJECTIVES

To assess characteristics of increased intracranial pressure (ICP) in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD).

METHODS

This is a multicenter retrospective review of 84 MOGAD cases at the University of Florida, Baylor College of Medicine, the University of California San Diego, and Providence Health and Services, Portland, Oregon, to identify cases with a documented increased opening pressure >25 cm H2O. A literature review was conducted to identify previously reported MOGAD cases with an opening pressure >25 cm H2O.

RESULTS

Of 28 MOGAD cases with available opening pressures, 6 (21.4%) patients (age: 5 to 36 y; 2/6 females) had documented increased ICP with an opening pressure of 26 to 46 cm H2O and optic nerve head edema on funduscopic examination. The increased ICP occurred in the setting of bilateral optic neuritis in all cases. In 5/6 patients, this was the initial presentation of the disorder. Anti-MOG titers were 1:40 (n = 1), 1:100 (n = 4), and 1:1000 (n = 1). In our literature review, we identified 13 additional MOGAD cases with ICP elevations in the setting of meningo-cortical presentations (n = 10), as well as bilateral optic neuritis (n = 3).

CONCLUSIONS

Increased ICP may occur in MOGAD and may be more common in patients with optic neuritis or meningoencephalitis.

摘要

目的

评估髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)中颅内压升高(ICP)的特征。

方法

这是一项对佛罗里达大学、贝勒医学院、加利福尼亚大学圣地亚哥分校以及俄勒冈州波特兰市普罗维登斯健康与服务中心的84例MOGAD病例进行的多中心回顾性研究,以确定记录的初压>25 cm H₂O升高的病例。进行文献回顾以确定先前报道的初压>25 cm H₂O的MOGAD病例。

结果

在28例有可用初压的MOGAD病例中,6例(21.4%)患者(年龄:5至36岁;2/6为女性)记录有ICP升高,初压为26至46 cm H₂O,眼底检查可见视神经乳头水肿。所有病例中ICP升高均发生在双侧视神经炎的情况下。5/6的患者中,这是该疾病的初始表现。抗MOG滴度为1:40(n = 1)、1:100(n = 4)和1:1000(n = 1)。在我们的文献回顾中,我们又发现了13例MOGAD病例,其ICP升高发生在脑膜-皮质表现(n = 10)以及双侧视神经炎(n = 3)的情况下。

结论

MOGAD中可能发生ICP升高,在视神经炎或脑膜脑炎患者中可能更常见。

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