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脑干磁共振病灶特征对脑干临床孤立综合征转归的预测价值

杨宁 龙友明 范永祥 单福兰 解龙昌 殷建瑞 蒲蜀湘 高庆春 高聪

广东医学Issue(16):2491-2494,4.
广东医学Issue(16):2491-2494,4.

脑干磁共振病灶特征对脑干临床孤立综合征转归的预测价值

Magnetic resonance imaging feature predicts the conversion in clinically isolated syndrome with pure brainstem lesions

杨宁 1龙友明 2范永祥 2单福兰 2解龙昌 2殷建瑞 2蒲蜀湘 2高庆春 2高聪2

作者信息

  • 1. 广州医科大学附属第五医院神经内科 广州510700
  • 2. 广州医科大学附属第二医院神经内科 广州510260
  • 折叠

摘要

Abstract

Objective To explore the MRI features of brainstem lesions in clinically isolated syndromes ( CIS) and evaluated their association with clinical conversion .Methods Patients with brainstem CIS were prospectively fol-lowed-up and brain MRI features were retrospectively analyzed .Results A total of 25 patients were followed -up for a median of 65 months.Neuromyelitis optica ( NMO), NMO spectrum disorder ( NMOSD) and multiple sclerosis ( MS) were observed in 5, 4 and 4 cases, respectively.According to MRI,"Fog-like"lesions were significantly more abundant in NMO+NMOSD patients than in MS patients (P=0.001) or stable patients (P<0.000 1).Extensive lesions were on-ly found in 5 (55.6%) patients with NMO+NMOSD.Aqueduct lesions were also significantly more frequently found in NMO+NMOSD patients than in MS patients (P=0.021) or stable patients (P=0.002).The sensitivity and specificity of"Fog-like"lesions in T2 -weight image for diagnosis of NMO +NMOSD were 100% and 93.75%, respectively;while the sensitivity and specificity of extensive lesions for diagnosis of NMO +NMOSD were 55.56%and 100%, respec-tively.The sensitivity and specificity of aqueduct lesions for diagnosis of NMO +NMOSD were 77.78%and 93.75%, re-spectively.Conclusion The "Fog-like", extensive and aqueduct lesions in the brainstem in MRI are important early markers for future NMO and NMOSD .

关键词

临床孤立综合征/视神经脊髓炎/多发性硬化/磁共振

Key words

MRI/clinically isolated syndrome/neuromyelitis optica

引用本文复制引用

杨宁,龙友明,范永祥,单福兰,解龙昌,殷建瑞,蒲蜀湘,高庆春,高聪..脑干磁共振病灶特征对脑干临床孤立综合征转归的预测价值[J].广东医学,2014,(16):2491-2494,4.

基金项目

广东省自然科学基金资助项目(编号S2013010016262),广东省科技计划项目 ()

广东医学

OA北大核心CSTPCD

1001-9448

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