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动脉自旋标记检测到的高灌注性急性脑病病例:扩展了具有双相性惊厥和后期弥散降低的急性脑病谱。

A case of acute encephalopathy with hyperperfusion detected by arterial spin labelling: Extending spectrum of acute encephalopathy with biphasic seizures and late reduced diffusion.

机构信息

Department of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Yachiyo, Japan.

Department of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Yachiyo, Japan.

出版信息

Brain Dev. 2024 Nov;46(10):388-391. doi: 10.1016/j.braindev.2024.09.007. Epub 2024 Sep 30.

DOI:10.1016/j.braindev.2024.09.007
Abstract

BACKGROUND

Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is the most common encephalopathy syndrome among Japanese children. We report, for the first time, a case of AESD, in which magnetic resonance imaging (MRI) showed no diffusion abnormalities, but hyperperfusion was detected by arterial spin labelling (ASL).

CASE REPORT

A previously healthy Japanese 1-year and 5-month-old boy was transferred to our hospital due to a consciousness disorder after >60 min of status epilepticus on the first day of fever. Brain MRI on the first day revealed no abnormal findings. On the fourth day, focal seizures of the left upper and lower limbs were observed. Thereafter, the patient's condition progressed without seizures. Diffusion-weighted imaging (DWI) on day 6 showed no abnormal findings, including a bright tree appearance. However, ASL showed hyperperfusion in the frontoparietal lobes. MRI scans on days 19 and 39 revealed that the hyperperfusion lesions on day 6 had transitioned to hypoperfusion on ASL and displayed high signal intensity on T2-weighted and fluid-attenuated inversion recovery imaging. Cerebral atrophy was also observed. Based on the clinical course and imaging findings during the chronic phase, a diagnosis of AESD was made.

CONCLUSION

ASL may be more sensitive than DWI for detecting AESD lesions and should be performed in children with suspected AESD.

摘要

背景

急性脑炎伴双相抽搐和后期弥散受限(AESD)是日本儿童中最常见的脑炎综合征。我们首次报告了一例 AESD 病例,磁共振成像(MRI)未显示弥散异常,但动脉自旋标记(ASL)显示高灌注。

病例报告

一名 1 岁零 5 个月大的既往健康的日本男孩,因发热第一天出现 60 多分钟的癫痫持续状态后出现意识障碍而转入我院。第一天的脑部 MRI 未见异常。第四天,观察到左上下肢局限性癫痫发作。此后,患者病情进展无癫痫发作。第 6 天的弥散加权成像(DWI)未见异常,包括亮树外观。然而,ASL 显示额顶叶高灌注。第 6 天的高灌注病变在第 19 天和第 39 天的 MRI 扫描中显示已转变为 ASL 低灌注,并在 T2 加权和液体衰减反转恢复成像上显示高信号强度。还观察到脑萎缩。根据慢性期的临床过程和影像学发现,诊断为 AESD。

结论

ASL 可能比 DWI 更敏感地检测 AESD 病变,对于疑似 AESD 的儿童应进行 ASL 检查。

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