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首页> 外文期刊>BMC Neurology >Wallerian degeneration of bilateral cerebral peduncles after acute carbon monoxide poisoning
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Wallerian degeneration of bilateral cerebral peduncles after acute carbon monoxide poisoning

机译:急性一氧化碳中毒后双侧脑梗死的Wallerian退化

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Cases of Wallerian degeneration of bilateral cerebral peduncles after acute carbon monoxide poisoning have not yet been reported. To date, most of the delayed encephalopathy after acute carbon monoxide poisoning (DEACMP) lesions captured in magnetic resonance imaging (MRI) has been located in the subcortical white matter and basal ganglia. Here we report two cases of DEACMP with abnormalities in the bilateral cerebral peduncles. The etiology of abnormalities, which were strictly confined to the bilateral cerebral peduncles, was Wallerian degeneration secondary to upstream nerve axonal damage, making this the first report on such bilateral cerebral peduncle abnormalities after DEACMP. In this report, we present two cases of DEACMP with abnormal signals in the bilateral cerebral peduncles captured during brain MRIs. Case 1 was of a 68-year-old man who presented with paroxysmal disturbance of the consciousness, left limb weakness for 16?days, and lagging responses for 2?days. Case 2 was of a 55-year-old man who was unconscious for 6?h. In addition to the above mentioned characteristics on the brain MRIs, the electroencephalography of case 1 indicated that his forehead scans had a mixture of wide sharp, sharp, and three-phase waves. Brain diffusion tensor imaging of case 2 further proved that the bilateral cerebral anomalies represented Wallerian degeneration secondary to upstream axonal damage. After the definitive diagnosis, the patients returned to the local hospital for hyperbaric oxygen therapy. Wallerian degeneration of the bilateral cerebral peduncles after acute carbon monoxide poisoning has never been reported before. The abnormal signals in the bilateral cerebral peduncles captured during brain MRIs indicated Wallerian degeneration secondary to upstream axonal damage; thus, these two cases may further our understanding of DEACMP imaging.
机译:尚未报道急性炭一氧化物中毒后双侧脑梗死的Wallerian退化案例。迄今为止,大多数延迟的脑病后,磁共振成像(MRI)中捕获的急性炭一氧化物中毒(DEACMP)病变已经位于皮质点白质和基底神经节。在这里,我们报告了两种患有双侧脑梗死异常的DEACMP病例。严格局限于双侧脑梗死的异常的病因,是次神经轴突损伤的Wallerian变性,使得第一份关于DEACP之后的双侧脑梗死异常的第一份报告。在本报告中,我们在脑部MRIS期间捕获的双侧脑梗死中的两种患者的DEACMP病例。案例1是一名68岁的男子,患有阵发性扰动的意识,留下肢体的弱点16?天,滞后2天。案例2是一个55岁的男人,6?h是无意识的。除了上述脑部MRIS的特征外,壳体1的脑电图表明他的额头扫描具有宽尖锐,尖锐和三相波的混合物。病例2的脑扩散张量成像进一步证明了双侧脑异常代表次级轴突损伤的次次次颅内变性。在明确的诊断后,患者返回当地医院进行高压氧疗。在急性炭一氧化物中毒后的双侧脑梗死的Wallerian退化从未报道过。在脑部MRIS期间捕获的双侧脑梗死的异常信号表明次级轴突造成的Wallerian变性;因此,这两种情况可能进一步了解DEACMP成像。

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