Pradeep K, Sinha S, Saini J, Mahadevan A, Arivazhagan A, Bharath R D, Bindu P S, Jamuna R, Rao M B, Chandramouli B A, Shankar S K, Satishchandra P
Department of Neurology, National Institute of Mental Health and NeuroSciences (NIMHANS), Bangalore, India.
Acta Neurol Scand. 2014 Oct;130(4):253-9. doi: 10.1111/ane.12212. Epub 2013 Dec 17.
We studied the MRI findings in 16 patients with Rasmussen's encephalitis (RE), further analysed serial MRI changes in 11 of them and correlated it with clinical features.
The diagnosis of RE was based on the European consensus statement (Brain, 128, 2005, 454). Details related to demographical, clinical, MRI observations were analysed.
Forty MRIs of brain of 16 patients were reviewed. Eleven patients had undergone serial brain MRIs ranging from two to five occasions. All the patients had unihemispheric focal cortical atrophy, predominantly in the perisylvian region (n = 13). Other features were white matter signal changes (n = 14), and ipsilateral caudate (n = 6) and putamen (n = 4) atrophy. Signal alterations in putamen and caudate were noted in four each. In all the 11 patients with serial MRI, there was progression of cerebral atrophy and a trend towards increase in MRI staging. The MRI signal changes remained same in five patients, resolved in three patients, differential change in two patients and increased in one patient. Diffusion-weighted imaging showed facilitated diffusion (n = 5), and MR spectroscopy showed reduced N-acetyl-aspartate and elevated lactate (n = 2).
Pattern recognition of MRI findings and the changes in serial MRI might serve as a surrogate marker of disease viz. unihemispheric progressive focal cortical atrophy and signal changes predominantly in the perisylvian distribution and caudate followed by putamen involvement. This might assist in understanding and monitoring of the disease progression.
我们研究了16例拉斯穆森脑炎(RE)患者的MRI表现,进一步分析了其中11例患者的MRI序列变化,并将其与临床特征相关联。
RE的诊断基于欧洲共识声明(《大脑》,128卷,2005年,454页)。分析了与人口统计学、临床、MRI观察相关的详细信息。
回顾了16例患者的40次脑部MRI检查。11例患者接受了2至5次的脑部MRI序列检查。所有患者均有单半球局灶性皮质萎缩,主要位于外侧裂周围区域(n = 13)。其他特征包括白质信号改变(n = 14),以及同侧尾状核(n = 6)和壳核(n = 4)萎缩。壳核和尾状核的信号改变各有4例。在所有11例接受序列MRI检查的患者中,均存在脑萎缩进展,且MRI分期有增加趋势。5例患者的MRI信号改变保持不变,3例患者的信号改变消失,2例患者的信号改变有差异,1例患者的信号改变增加。弥散加权成像显示扩散加快(n = 5),磁共振波谱显示N - 乙酰天门冬氨酸降低和乳酸升高(n = 2)。
MRI表现的模式识别以及序列MRI的变化可能作为疾病的替代标志物,即单半球进行性局灶性皮质萎缩以及主要在外侧裂分布区域和尾状核随后累及壳核的信号改变。这可能有助于理解和监测疾病进展。