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潘纳约托普洛斯综合征中海马体的信号变化及棘波的电流源

Signal change in hippocampus and current source of spikes in Panayiotopoulos syndrome.

作者信息

Yeom Jung Sook, Kim Youngsoo, Park Ji Sook, Seo Ji Hyun, Park Eun Sil, Lim Jae Young, Park Chan-Hoo, Woo Hyang Ok, Youn Hee-Shang, Kwon Oh-Young

机构信息

Department of Pediatrics, Gyeongsang National University School of Medicine, Jinju, Korea.

出版信息

Korean J Pediatr. 2012 Feb;55(2):63-7. doi: 10.3345/kjp.2012.55.2.63. Epub 2012 Feb 14.

Abstract

A 4-year-old girl with Panayiotopoulos syndrome presented with a history of 4 prolonged autonomic seizures. The clinical features of her seizures included, in order of occurrence, blank staring, pallor, vomiting, hemi-clonic movement on the right side, and unresponsiveness. A brain magnetic resonance imaging (MRI) showed a slightly high T(2) signal in the left hippocampus. Interictal electoencephalogram revealed spikes in the occipital area of the left hemisphere. We analyzed the current-source distribution of the spikes to examine the relationship between the current source and the high T(2) signal. The current source of the occipital spikes was not only distributed in the occipital area of both cerebral hemispheres, but also extended to the posterior temporal area of the left hemisphere. These findings suggest that the left temporal lobe may be one of the hyperexcitable areas and form part of the epileptogenic area in this patient. We hypothesized that the high T(2) signal in the left hippocampus of our patient may not have been an incidental lesion, but instead may be related to the underlying electroclinical diagnosis of Panayiotopoulos syndrome, and particularly seizure. This notion is important because an abnormal T(2) signal in the hippocampus may represent an acute stage of hippocampal injury, although there is no previous report of hippocampal pathology in Panayiotopoulos syndrome. Therefore, long-term observation and serial follow-up MRIs may be needed to confirm the clinical significance of the T(2) signal change in the hippocampus of this patient.

摘要

一名患有潘纳约托普洛斯综合征的4岁女孩有4次长时间自主神经发作史。她发作的临床特征依次为发呆凝视、面色苍白、呕吐、右侧半身阵挛运动和无反应。脑部磁共振成像(MRI)显示左侧海马体T(2)信号略高。发作间期脑电图显示左半球枕区有棘波。我们分析了棘波的电流源分布,以研究电流源与高T(2)信号之间的关系。枕部棘波的电流源不仅分布在双侧大脑半球的枕区,还延伸至左半球颞叶后部。这些发现表明,左颞叶可能是该患者的高兴奋性区域之一,也是致痫区的一部分。我们推测,该患者左侧海马体的高T(2)信号可能并非偶然病变,而是可能与潘纳约托普洛斯综合征的潜在电临床诊断,尤其是发作有关。这一观点很重要,因为海马体中的异常T(2)信号可能代表海马体损伤的急性期,尽管之前没有关于潘纳约托普洛斯综合征中海马体病理学的报道。因此,可能需要长期观察和系列随访MRI来确认该患者海马体T(2)信号变化的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a6/3286765/564ab92311b5/kjped-55-63-g001.jpg

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