Acute Disseminated Encephalomyelitis Presenting as Bilateral Ptosis in a Sri Lankan Child.

IF 0.7 Q4 PEDIATRICS
Case Reports in Pediatrics Pub Date : 2022-02-08 eCollection Date: 2022-01-01 DOI:10.1155/2022/5492155
Ishara Kumarasiri, Ruwan Samararathna, Udara Sandakelum, Oshanie Muthukumarana, Reha Balasubramaniam, Sachith Mettananda
{"title":"Acute Disseminated Encephalomyelitis Presenting as Bilateral Ptosis in a Sri Lankan Child.","authors":"Ishara Kumarasiri,&nbsp;Ruwan Samararathna,&nbsp;Udara Sandakelum,&nbsp;Oshanie Muthukumarana,&nbsp;Reha Balasubramaniam,&nbsp;Sachith Mettananda","doi":"10.1155/2022/5492155","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Acute disseminated encephalomyelitis is a rare inflammatory demyelinating disease characterized by acute onset polyfocal neurological deficits associated with encephalopathy. It commonly presents with fever, meningism, seizures, ataxia, motor deficits, and bladder dysfunction. Although cranial neuropathies, including optic neuritis and facial nerve palsies, have previously been reported, children presenting with bilateral ptosis is extremely rare. Here, we report a 3-year-old child with acute disseminated encephalomyelitis presenting with acute onset bilateral ptosis due to involvement of the single central levator subnucleus of the oculomotor nerve. <i>Case Presentation</i>. A 3-year-old Sri Lankan boy presented with drooping of the upper eyelids for three days and unsteady gait for two days. He did not have seizures, blurring of vision, limb weakness, swallowing or breathing difficulties, or bladder dysfunction. On examination, he had bilateral ptosis, gait ataxia, and dysmetria. His vision, eye movements, and examination of other cranial nerves were normal. MRI brain revealed high signal intensities involving the subcortical white matter of parietal and occipital lobes, midbrain in the area of single central levator subnucleus of the oculomotor nerve, cerebellar vermis, and right cerebellar hemisphere. Based on the clinical features suggesting polyfocal neurological involvement of the midbrain and cerebellum and characteristic MRI findings, the diagnosis of acute disseminated encephalomyelitis was made. He responded well and rapidly to high-dose intravenous methylprednisolone and showed a complete clinical and radiological recovery.</p><p><strong>Conclusion: </strong>This case report describes a rare presentation of acute disseminated encephalomyelitis, bilateral ptosis due to involvement of the single central levator subnucleus of the oculomotor nerve. It highlights that the presenting manifestations of acute disseminated encephalomyelitis can be subtle and vary; however, timely diagnosis and treatment result in complete recovery.</p>","PeriodicalId":9623,"journal":{"name":"Case Reports in Pediatrics","volume":null,"pages":null},"PeriodicalIF":0.7000,"publicationDate":"2022-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847039/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2022/5492155","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Acute disseminated encephalomyelitis is a rare inflammatory demyelinating disease characterized by acute onset polyfocal neurological deficits associated with encephalopathy. It commonly presents with fever, meningism, seizures, ataxia, motor deficits, and bladder dysfunction. Although cranial neuropathies, including optic neuritis and facial nerve palsies, have previously been reported, children presenting with bilateral ptosis is extremely rare. Here, we report a 3-year-old child with acute disseminated encephalomyelitis presenting with acute onset bilateral ptosis due to involvement of the single central levator subnucleus of the oculomotor nerve. Case Presentation. A 3-year-old Sri Lankan boy presented with drooping of the upper eyelids for three days and unsteady gait for two days. He did not have seizures, blurring of vision, limb weakness, swallowing or breathing difficulties, or bladder dysfunction. On examination, he had bilateral ptosis, gait ataxia, and dysmetria. His vision, eye movements, and examination of other cranial nerves were normal. MRI brain revealed high signal intensities involving the subcortical white matter of parietal and occipital lobes, midbrain in the area of single central levator subnucleus of the oculomotor nerve, cerebellar vermis, and right cerebellar hemisphere. Based on the clinical features suggesting polyfocal neurological involvement of the midbrain and cerebellum and characteristic MRI findings, the diagnosis of acute disseminated encephalomyelitis was made. He responded well and rapidly to high-dose intravenous methylprednisolone and showed a complete clinical and radiological recovery.

Conclusion: This case report describes a rare presentation of acute disseminated encephalomyelitis, bilateral ptosis due to involvement of the single central levator subnucleus of the oculomotor nerve. It highlights that the presenting manifestations of acute disseminated encephalomyelitis can be subtle and vary; however, timely diagnosis and treatment result in complete recovery.

Abstract Image

Abstract Image

斯里兰卡儿童急性播散性脑脊髓炎表现为双侧上睑下垂。
简介:急性播散性脑脊髓炎是一种罕见的炎症性脱髓鞘疾病,其特征是急性发作的多灶性神经功能缺损与脑病相关。它通常表现为发热、脑膜炎、癫痫、共济失调、运动障碍和膀胱功能障碍。虽然颅神经病变,包括视神经炎和面神经麻痹,以前有报道,儿童表现为双侧上睑下垂是极其罕见的。在这里,我们报告了一个3岁的儿童急性播散性脑脊髓炎,表现为急性发作的双侧上睑下垂,由于单侧中央提肌亚核的动眼神经受累。案例演示。斯里兰卡3岁男童,上眼睑下垂3天,步态不稳2天。他没有癫痫发作、视力模糊、四肢无力、吞咽或呼吸困难,也没有膀胱功能障碍。经检查,他有双侧上睑下垂、步态共济失调和节律障碍。他的视力、眼球运动和其他脑神经检查正常。脑MRI显示高信号强度累及顶叶和枕叶皮质下白质、动眼神经单个中央提肌亚核区域中脑、小脑蚓部和右脑半球。根据中脑和小脑多局灶性神经系统受累的临床特征和特征性MRI表现,诊断为急性播散性脑脊髓炎。他对大剂量静脉注射甲基强的松龙反应良好,迅速,临床和放射学完全恢复。结论:这个病例报告描述了一个罕见的急性播散性脑脊髓炎,双侧上睑下垂,由于单侧中央提肌亚核的动眼神经受累。它强调急性播散性脑脊髓炎的表现可以是微妙的和多样的;然而,及时的诊断和治疗导致完全康复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
11.10%
发文量
48
审稿时长
13 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信