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[孤立性视神经炎发作后多发性硬化症的发展。磁共振研究]

[The development of multiple sclerosis following an isolated episode of optic neuritis. Magnetic resonance study].

作者信息

Río J, Nos C, Rovira A, Tintoré M, Codina A, Montalbán X

机构信息

Unitat d'Esclerosi Múltiple, Hospital General Univérsitari Vall d'Hebron, Barcelona.

出版信息

Med Clin (Barc). 1997 Sep 27;109(10):370-2.

PMID:9379718
Abstract

BACKGROUND

An important controversy on the development of multiple sclerosis (MS) after an isolated episode of optic neuritis (ON) exists. Magnetic resonance imaging (MRI) is the method of election in order to detect demyelinated lesions in MS. The current study was designed to determine the prevalence of brain abnormalities on MRI and to asses the further development of MS after an isolated idiopathic ON in our population.

PATIENTS AND METHODS

From 1991 to 1995, 60 patients with decrease of visual acuity were studied, 35 (28 women, half age 31 +/- 10 years) completed criteria of idiopathic ON. A brain MRI was performed in all patients after the diagnosis of idiopathic ON and they subsequently were followed in the outpatient clinic from our center for a mean time of 29 +/- 16 months. 24 out of the 35 patients were treated with corticosteroids in different ways.

RESULTS

It has been found 43% of the patients with idiopathic ON to have brain lesions by MRI. During the follow-up 14% of the patients developed a clinically definite MS; all of them had a pathological brain MRI at the basal evaluation (p = 0.009). None of the patients that were treated with high-dose of intravenously corticosteroids developed MS.

CONCLUSIONS

The prevalence of silent cerebral lesions in the MRI after an idiopathic ON is elevated in our population although further development of MS is lower possibly due to the short follow-up carried out. The presence of lesions in the MRI confers a high risk for developing MS after an idiopathic ON.

摘要

背景

孤立性视神经炎(ON)发作后多发性硬化症(MS)的发展存在重要争议。磁共振成像(MRI)是检测MS中脱髓鞘病变的首选方法。本研究旨在确定MRI上脑异常的患病率,并评估我们人群中孤立性特发性ON后MS的进一步发展情况。

患者与方法

1991年至1995年,对60例视力下降患者进行了研究,其中35例(28例女性,平均年龄31±10岁)符合特发性ON标准。所有患者在诊断为特发性ON后均进行了脑部MRI检查,随后在我们中心的门诊随访,平均时间为29±16个月。35例患者中有24例接受了不同方式的皮质类固醇治疗。

结果

发现43%的特发性ON患者通过MRI检查有脑部病变。在随访期间,14%的患者发展为临床确诊的MS;所有这些患者在基线评估时脑部MRI均有异常(p = 0.009)。接受大剂量静脉注射皮质类固醇治疗的患者均未发生MS。

结论

在我们的人群中,特发性ON后MRI上无症状脑病变的患病率较高,尽管由于随访时间短,MS的进一步发展可能较低。MRI上有病变表明特发性ON后发生MS的风险很高。

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