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一例患有可逆性胼胝体压部病变的轻度脑病/脑炎新生儿病例。

A Neonatal Case of Mild Encephalopathy/Encephalitis with a Reversible Splenial Lesion.

作者信息

Oki Yuzuki, Yoshida Tomohide, Yogi Akira, Kurokawa Shingo, Goya Hideki, Tsukayama Mayumi, Nakamura Sadao, Mekaru Keiko, Nakanishi Koichi

机构信息

Department of Child Health and Welfare, Graduate School of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan.

Maternity and Perinatal Care Center, University of the Ryukyus Hospital, Nishihara, Okinawa, Japan.

出版信息

Child Neurol Open. 2022 Aug 1;9:2329048X221111716. doi: 10.1177/2329048X221111716. eCollection 2022 Jan-Dec.

Abstract

The neurological symptoms of pediatric mild encephalopathy/encephalitis with a reversible splenial lesion (MERS) are mild and have a good prognosis. However, some aspects of neonatal MERS are unclear due to a lack of clinical knowledge. We present a neonatal case of MERS with features of poor activity and prolonged poor oxygenation after birth without asphyxia. He was diagnosed with MERS by brain magnetic resonance imaging (MRI) on day10, because the diffusion restriction of the splenium of the corpus callosum (SCC) seen on diffusion-weighted MRI on day 5 was attenuating. He was discharged due to good progress on day 26, but growth issues and developmental delay were observed in the follow up from 1-10 months. In rare neonatal cases, many aspects of the clinical course and prognosis are thus unclear. MERS should be considered in newborns who show unexplained non-neural or other encephalopathic symptoms.

摘要

小儿轻度脑病/伴有可逆性胼胝体压部病变的脑炎(MERS)的神经症状较轻,预后良好。然而,由于缺乏临床知识,新生儿MERS的一些方面尚不清楚。我们报告一例新生儿MERS病例,其特征为出生后活动不佳且无窒息情况下存在长时间低氧血症。出生第10天通过脑磁共振成像(MRI)诊断为MERS,因为出生第5天扩散加权MRI上所见胼胝体压部(SCC)的扩散受限情况正在减轻。患儿于第26天因病情好转出院,但在1至10个月的随访中观察到生长问题和发育迟缓。因此,在罕见的新生儿病例中,临床病程和预后的许多方面尚不清楚。对于出现无法解释的非神经或其他脑病症状的新生儿,应考虑MERS的可能。

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Two newly proposed infectious encephalitis/encephalopathy syndromes.两种新提出的感染性脑炎/脑病综合征。
Brain Dev. 2009 Aug;31(7):521-8. doi: 10.1016/j.braindev.2009.02.012. Epub 2009 Mar 31.
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Neonate showing reversible splenial lesion.新生儿出现可逆性胼胝体病变。
Arch Neurol. 2005 Sep;62(9):1481-2; author reply 1482. doi: 10.1001/archneur.62.9.1481.

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