Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room.

IF 0.8 Q4 CLINICAL NEUROLOGY
Iranian Journal of Child Neurology Pub Date : 2024-01-01 Epub Date: 2024-09-29 DOI:10.22037/ijcn.v18i4.43749
Sareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, Maryam Bemanalizadeh, Masood Ghahvechi Akbari, Sanaz Rezaei, Nima Parvaneh, Morteza Heidari, Mohammad Vafaee-Shahi, Firouzeh Hosseini, Sayna Bagheri, Ali Reza Tavasoli
{"title":"Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room.","authors":"Sareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, Maryam Bemanalizadeh, Masood Ghahvechi Akbari, Sanaz Rezaei, Nima Parvaneh, Morteza Heidari, Mohammad Vafaee-Shahi, Firouzeh Hosseini, Sayna Bagheri, Ali Reza Tavasoli","doi":"10.22037/ijcn.v18i4.43749","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Acute Flaccid Paralysis (AFP) in children can stem from a diverse array of potential diagnoses.</p><p><strong>Materials & methods: </strong>This retrospective study sought to diagnose children referred to a referral pediatric emergency unit with AFP between 2011 and 2016. The study gathered clinical observations, conducted stool and cerebrospinal fluid analyses, and assessed electrophysiological and imaging data.</p><p><strong>Results: </strong>The present study enrolled 118 fully immunized children with a mean age of 6.09 ± 3.60 years. The most prevalent diagnoses included Guillain-Barré Syndrome (GBS-80 cases), acute viral myositis (20 cases), Transverse Myelitis Syndrome (TMS) (TMS-6 cases), and Vaccine-Associated Paralytic Poliomyelitis (VAPP) (VAPP-6 cases). All these six patients had primary immunodeficiency. Notably, all patients tested negative for poliovirus in stool analyses. This study encountered a unique case of a 2.5-month-old male patient who presented with acute limb motor weakness, along with fever, irritability, new-onset hypotonia, and generalized decreased deep tendon reflexes. Notably, no signs of upper motor neuron involvement were found. The Cerebrospinal Fluid (CSF) analysis was compatible with the diagnosis of viral meningitis. Moreover, among the 60 brain and spinal imaging series performed, five were indicative of GBS, six cases showed evidence of TMS, and one revealed a spinal mass. Besides, clinical investigations pointed toward acute viral myositis as a secondary etiology of AFP in 20 patients in this study.</p><p><strong>Conclusion: </strong>In this hospital-based study, the most frequent diagnoses for children arriving at a third-level pediatric Emergency Room (ER) with acute flaccid paralysis AFP were GBS, acute viral myositis, TMS, and VAPP). These findings suggest a distinct pattern of AFP causes compared to those found in community-based epidemiological studies. Additionally, notably, unusual conditions, such as viral meningitis, can rarely present with AFP-like symptoms. Assessment for primary immune deficiency should be considered in cases of VAPP. Lastly, this research has implemented a pediatric AFP Management Protocol: A Local Practical Approach.</p>","PeriodicalId":14537,"journal":{"name":"Iranian Journal of Child Neurology","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520268/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Child Neurology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22037/ijcn.v18i4.43749","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/29 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Acute Flaccid Paralysis (AFP) in children can stem from a diverse array of potential diagnoses.

Materials & methods: This retrospective study sought to diagnose children referred to a referral pediatric emergency unit with AFP between 2011 and 2016. The study gathered clinical observations, conducted stool and cerebrospinal fluid analyses, and assessed electrophysiological and imaging data.

Results: The present study enrolled 118 fully immunized children with a mean age of 6.09 ± 3.60 years. The most prevalent diagnoses included Guillain-Barré Syndrome (GBS-80 cases), acute viral myositis (20 cases), Transverse Myelitis Syndrome (TMS) (TMS-6 cases), and Vaccine-Associated Paralytic Poliomyelitis (VAPP) (VAPP-6 cases). All these six patients had primary immunodeficiency. Notably, all patients tested negative for poliovirus in stool analyses. This study encountered a unique case of a 2.5-month-old male patient who presented with acute limb motor weakness, along with fever, irritability, new-onset hypotonia, and generalized decreased deep tendon reflexes. Notably, no signs of upper motor neuron involvement were found. The Cerebrospinal Fluid (CSF) analysis was compatible with the diagnosis of viral meningitis. Moreover, among the 60 brain and spinal imaging series performed, five were indicative of GBS, six cases showed evidence of TMS, and one revealed a spinal mass. Besides, clinical investigations pointed toward acute viral myositis as a secondary etiology of AFP in 20 patients in this study.

Conclusion: In this hospital-based study, the most frequent diagnoses for children arriving at a third-level pediatric Emergency Room (ER) with acute flaccid paralysis AFP were GBS, acute viral myositis, TMS, and VAPP). These findings suggest a distinct pattern of AFP causes compared to those found in community-based epidemiological studies. Additionally, notably, unusual conditions, such as viral meningitis, can rarely present with AFP-like symptoms. Assessment for primary immune deficiency should be considered in cases of VAPP. Lastly, this research has implemented a pediatric AFP Management Protocol: A Local Practical Approach.

探索急性弛缓性麻痹的表型特征:来自三级儿科急诊室的启示。
目的:儿童急性弛缓性麻痹(AFP)的潜在诊断多种多样:儿童急性弛缓性麻痹(AFP)的潜在诊断多种多样:这项回顾性研究旨在诊断2011年至2016年期间转诊至儿科急诊室的急性弛缓性麻痹患儿。研究收集了临床观察结果,进行了粪便和脑脊液分析,并评估了电生理学和影像学数据:本研究共纳入 118 名完全免疫的儿童,平均年龄为(6.09 ± 3.60)岁。最常见的诊断包括吉兰-巴雷综合征(GBS-80 例)、急性病毒性肌炎(20 例)、横贯性脊髓炎综合征(TMS)(TMS-6 例)和疫苗相关麻痹性脊髓灰质炎(VAPP)(VAPP-6 例)。这六名患者均患有原发性免疫缺陷。值得注意的是,所有患者的粪便分析结果均为阴性。本研究发现了一例特殊病例,一名 2.5 个月大的男性患者出现急性肢体运动无力,伴有发热、烦躁、新发肌张力低下和全身深腱反射减弱。值得注意的是,没有发现上运动神经元受累的迹象。脑脊液(CSF)分析符合病毒性脑膜炎的诊断。此外,在 60 例脑和脊柱造影检查中,5 例显示为 GBS,6 例显示为 TMS,1 例显示为脊柱肿块。此外,临床调查显示,本研究中有 20 例患者的急性病毒性肌炎是 AFP 的继发病因:在这项以医院为基础的研究中,因急性弛缓性麻痹(AFP)前往三级儿科急诊室就诊的儿童最常见的诊断是GBS、急性病毒性肌炎、TMS和VAPP)。这些发现表明,与社区流行病学研究中发现的病因相比,急性弛缓性麻痹的病因模式截然不同。此外,值得注意的是,病毒性脑膜炎等不常见疾病很少会出现类似 AFP 的症状。在 VAPP 病例中,应考虑对原发性免疫缺陷进行评估。最后,本研究实施了儿科 AFP 管理程序:本地实用方法》。
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
CiteScore
1.40
自引率
0.00%
发文量
35
×
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