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Magnetic resonance imaging features in seizures associated with nonketotic hyperglycemia

机译:非酮症高血糖发作的磁共振成像特征

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Sir,A 57-year-old female was admitted for episodic clonic jerks affecting her right face and arm, each episode lasting for approximately 2' of 10 days duration. There was no improvement of jerks with carbamazepine, instead there was increase in the frequency (every 5') and also developed right upper limb weakness. Past medical history was negative. Neurological examination revealed right hemiparesia. Admission serum glucose was 29.8 mmol/L with no ketone bodies in the urine; serum sodium was 133.8 mmol/L and potassium was 3.5 mmol/L; blood urea nitrogen was 6.0 mmol/L and calculated serum osmolality was 310.4 mmol/L. Admission computed tomography was normal. Electroencephalography (EEG) revealed inter-ictal epileptiform discharges around the left central sulcus [Figure la-c]. Brain magnetic resonance imaging (MRI) [Figure 2] done on day 2 of admission showed subcortical hypointensity signal changes in the left parietal region on T2-weighted (T2-W), fluid attenuated inversion recovery (FLAIR) and diffusion-weighted imaging (DWI). Apparent diffusion coefficient (ADC) map showed isointensity in the corresponding region. Overlying cortical showed hyperintensity on FLAIR, DWI sequences and hypointensity on ADC map. The ADC values in cortical and subcortical lesions were lower than contralateral normal regions, especially in cortical lesions. Tl-W sequences were normal. She was diagnosed as epileptia partialis continua (EPC) associated with nonketotic hyperglycemia (NKH). Carbamazepine was stopped and intravenous insulin therapy was started. She had good glycemic control and the jerking remitted completely within 72 h. Follow up MRI at 5 months showed complete resolution of cortical hyperintensity and subcortical hypointensity.
机译:主席先生,一名57岁的女性因发作性阵挛性抽搐而影响了她的右脸和手臂,每次发作持续10天,时间约2'。卡马西平对抽搐没有改善,反而频率增加(每5')并且右上肢无力。既往病史为阴性。神经系统检查发现右偏瘫。入院血糖为29.8 mmol / L,尿中无酮体。血清钠为133.8 mmol / L,钾为3.5 mmol / L;血尿素氮为6.0 mmol / L,计算的血清渗透压为310.4 mmol / L。入院的计算机体层摄影术正常。脑电图(EEG)显示左中央沟周围出现发作性癫痫样放电[图la-c]。入院第2天进行的脑磁共振成像(MRI)[图2]显示,在T2加权(T2-W),液体衰减反转恢复(FLAIR)和弥散加权成像( DWI)。表观扩散系数(ADC)图显示相应区域的等强度。上层皮层在FLAIR,DWI序列上显示高强度,在ADC图上显示低强度。皮质和皮质下病变的ADC值低于对侧正常区域,尤其是皮质病变。 T1-W序列是正常的。她被诊断为伴有非酮症高血糖症(NKH)的部分癫痫持续性发作(EPC)。停用卡马西平并开始静脉注射胰岛素治疗。她的血糖控制良好,抽搐在72小时内完全缓解。在5个月时进行的MRI扫描显示皮质高强度和皮质下低强度完全消失。

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