Raghavendra S, Ashalatha R, Thomas Sanjeev V, Kesavadas C
Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, 695011 Kerala, India.
Neuroradiology. 2007 Apr;49(4):299-305. doi: 10.1007/s00234-006-0189-6. Epub 2007 Jan 3.
Neuroimaging in seizures associated with nonketotic hyperglycemia (NKH) is considered normal. We report magnetic resonance imaging (MRI) abnormalities in four patients with NKH and seizures.
We prospectively evaluated clinical and radiological abnormalities in four patients with NKH during the period March 2004 to December 2005.
All patients presented with seizures, either simple or complex partial seizures or epilepsia partialis continua. Two of them had transient hemianopia. MRI showed subcortical T2 hypointensity in the occipital white matter and in or around the central sulcus (two patients each), T2 hyperintensity of the overlying cortex (two patients), focal overlying cortical enhancement (three patients) and bilateral striatal hyperintensity (one patient). Diffusion-weighted imaging (DWI) performed in three patients showed restricted diffusion. The ictal semiology and electroencephalographic (EEG) findings correlated with the MRI abnormalities. On clinical recovery, the subcortical T2 hypointensity and striatal hyperintensity reversed in all patients. The initial cortical change evolved to FLAIR hyperintensity suggestive of focal cortical gliosis. The radiological differential diagnosis considered initially included encephalitis, malignancy and hemorrhagic infarct rendering a diagnostic dilemma.
We identified subcortical T2 hypointensity rather than hyperintensity as a characteristic feature of seizures associated with NKH. Only very few similar reports exist in literature. Reversible bilateral striatal T2 hyperintensity in NKH has not been reported to the best of our knowledge.
与非酮症高血糖症(NKH)相关的癫痫发作的神经影像学表现被认为是正常的。我们报告了4例NKH合并癫痫发作患者的磁共振成像(MRI)异常情况。
我们前瞻性评估了2004年3月至2005年12月期间4例NKH患者的临床和放射学异常情况。
所有患者均出现癫痫发作,包括简单部分性发作、复杂部分性发作或持续性部分性癫痫。其中2例有短暂性偏盲。MRI显示枕叶白质、中央沟内或中央沟周围皮质下T2低信号(各2例),上方皮质T2高信号(2例),局部上方皮质强化(3例)及双侧纹状体高信号(1例)。3例行弥散加权成像(DWI)检查的患者显示弥散受限。发作期症状学和脑电图(EEG)结果与MRI异常相关。临床恢复时,所有患者的皮质下T2低信号和纹状体高信号均消失。最初的皮质改变演变为液体衰减反转恢复序列(FLAIR)高信号,提示局灶性皮质胶质增生。最初考虑的放射学鉴别诊断包括脑炎、恶性肿瘤和出血性梗死,这造成了诊断困境。
我们发现皮质下T2低信号而非高信号是NKH相关癫痫发作的特征性表现。文献中仅有极少数类似报道。据我们所知,尚未有关于NKH中可逆性双侧纹状体T2高信号的报道。