MULTIPLE SCLEROSIS IN A CHILD. CLINICAL CASE

A.K. Mammadbəyli, S.E. Aliyeva
{"title":"MULTIPLE SCLEROSIS IN A CHILD. CLINICAL CASE","authors":"A.K. Mammadbəyli, S.E. Aliyeva","doi":"10.61788/njn.v1i23.20","DOIUrl":null,"url":null,"abstract":"Introduction. Pediatric-onset multiple sclerosis (POMS) is defined as MS with onset before 18 years of age, using the 2017 McDonald Criteria. 3-5% of all MS cases have pediatric onset. Mean age of onset in POMS is 11 years, however, most patients are older than 15. There is a known female predilection for MS, although not in the younger than 11 years age group. Materials and methods. Our article presents a clinical case of MS in children. We think that this information will be interesting for neurologists and pediatricians. Results. Our patient is a boy 13 years, born from the 3 pregnancy, 3 birth. His development was appropriate for his age. There is no patient with multiple sclerosis in the offspring. Symptoms started with blurred vision in one eye when he was 11 years old. He was under the supervision of a neurologist and received treatment. His condition has stabilized. Symptoms repeated after 6 months. In addition to the weakness of vision, there is also a difficulty in performing precise movements. In neurological status: Pupils reaction to light was preserved. Left-sided oculomotor deficiency is noted. Swallowing and hearing N. In the motor sphere: peripheral muscle tone D=S, hypotonia, reflexes D=S, hyperreflexia, muscle strength D=S, normal. Reflexogenic zones in the lower limbs have expanded. Sensory system without any changes. He is unstable in the Romberg state. In finger- nose test intentional tremor is seen. Brain MRI: active demyelinating lesions (largest 14x8) in supratentorial and infratentorial region. Spine MRI: contrast enhancing demyelinating lesions in C1 and C5. 3 months later, an increase of demyelinating lesions was noted in the MRI examination of the brain and spinal cord. Ophthalmologist's examination: retrobulbar neuritis. LP: Oligoclonal band was positive. General and biochemical analysis of blood was normal. Conclusion. There is quite a lot of information about multiple sclerosis in adults in the literature. However, it has not been adequately studied in children. Thus, we believe that studying the characteristics of the course of multiple sclerosis in the pediatric population is important and of social importance.","PeriodicalId":18831,"journal":{"name":"NATIONAL JOURNAL OF NEUROLOGY","volume":"54 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NATIONAL JOURNAL OF NEUROLOGY","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.61788/njn.v1i23.20","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction. Pediatric-onset multiple sclerosis (POMS) is defined as MS with onset before 18 years of age, using the 2017 McDonald Criteria. 3-5% of all MS cases have pediatric onset. Mean age of onset in POMS is 11 years, however, most patients are older than 15. There is a known female predilection for MS, although not in the younger than 11 years age group. Materials and methods. Our article presents a clinical case of MS in children. We think that this information will be interesting for neurologists and pediatricians. Results. Our patient is a boy 13 years, born from the 3 pregnancy, 3 birth. His development was appropriate for his age. There is no patient with multiple sclerosis in the offspring. Symptoms started with blurred vision in one eye when he was 11 years old. He was under the supervision of a neurologist and received treatment. His condition has stabilized. Symptoms repeated after 6 months. In addition to the weakness of vision, there is also a difficulty in performing precise movements. In neurological status: Pupils reaction to light was preserved. Left-sided oculomotor deficiency is noted. Swallowing and hearing N. In the motor sphere: peripheral muscle tone D=S, hypotonia, reflexes D=S, hyperreflexia, muscle strength D=S, normal. Reflexogenic zones in the lower limbs have expanded. Sensory system without any changes. He is unstable in the Romberg state. In finger- nose test intentional tremor is seen. Brain MRI: active demyelinating lesions (largest 14x8) in supratentorial and infratentorial region. Spine MRI: contrast enhancing demyelinating lesions in C1 and C5. 3 months later, an increase of demyelinating lesions was noted in the MRI examination of the brain and spinal cord. Ophthalmologist's examination: retrobulbar neuritis. LP: Oligoclonal band was positive. General and biochemical analysis of blood was normal. Conclusion. There is quite a lot of information about multiple sclerosis in adults in the literature. However, it has not been adequately studied in children. Thus, we believe that studying the characteristics of the course of multiple sclerosis in the pediatric population is important and of social importance.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
儿童多发性硬化症。临床病例
导言。根据 2017 年麦克唐纳标准,儿童发病型多发性硬化症(POMS)是指在 18 岁之前发病的多发性硬化症。在所有多发性硬化症病例中,3%-5%为儿童发病。POMS 的平均发病年龄为 11 岁,但大多数患者年龄超过 15 岁。众所周知,多发性硬化症有女性偏好,但在小于 11 岁的年龄组中没有女性偏好。材料和方法。本文介绍了一例儿童多发性硬化症的临床病例。我们认为,神经科医生和儿科医生会对这些信息感兴趣。结果。我们的患者是一名 13 岁男孩,3 胎 3 产。他的发育符合他的年龄。他的后代中没有多发性硬化症患者。症状始于 11 岁时的单眼视力模糊。他在神经科医生的指导下接受了治疗。他的病情已经稳定。6 个月后症状再次出现。除了视力减弱外,做精确的动作也有困难。在神经状况方面瞳孔对光的反应保持正常。左侧眼球运动障碍。运动方面:外周肌张力 D=S,肌张力低下,反射 D=S,反射亢进,肌力 D=S,正常。下肢反射区扩大。感觉系统无任何变化。朗伯格状态不稳定。指鼻试验中可见有意震颤。脑部核磁共振成像:脑室上部和脑室下部有活动性脱髓鞘病变(最大 14x8)。脊柱磁共振成像:C1和C5出现对比增强的脱髓鞘病变。3 个月后,大脑和脊髓的核磁共振检查发现脱髓鞘病变增加。眼科医生检查:球后神经炎。LP:少克隆带呈阳性。血液常规和生化分析正常。结论有关成人多发性硬化症的文献资料很多。然而,对儿童多发性硬化症的研究还不够充分。因此,我们认为研究多发性硬化症在儿童群体中的病程特点非常重要,具有重要的社会意义。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
SPINAL SURGERY: HISTORICAL ASPECTS AND CONTEMPORARY APPROACHES IN THE TREATMENT OF DEGENERATIVE DISORDERS MYELOPROLIFERATIVE DISEASES AS A CAUSE OF ACUTE CEREBROVASCULAR ACCIDENT NEUROFIBROMATOSIS TYPE 1. CLINICAL CASE EVALUATION OF OPTIC NERVE CHANGES IN PATIENTS WITH MULTIPLE SCLEROSIS USING OPTICAL COHERENCE TOMOGRAPHY METHODOLOGICAL BASIS FOR STUDYING THE MEDICOSOCIAL CONSEQUENCES OF THE FEMALE REPRODUCTIVE SYSTEM ON THE BACKGROUND OF MULTIPLE SCLEROSIS
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1