Hosseinpour Sareh, Pazouki Roxana, Ashrafi Mahmoud Reza, Bemanalizadeh Maryam, Ghahvechi Akbari Masood, Rezaei Sanaz, Parvaneh Nima, Heidari Morteza, Vafaee-Shahi Mohammad, Hosseini Firouzeh, Bagheri Sayna, Tavasoli Ali Reza
Pediatric Neurologist, Myelin Disorders Clinic, Pediatric Neurology Division, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Pediatric Neurologist, Department of Pediatric Neurology, Vali-e-Asr Hospital, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Child Neurol. 2024 Fall;18(4):33-45. doi: 10.22037/ijcn.v18i4.43749. Epub 2024 Sep 29.
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.
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.
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.
儿童急性弛缓性麻痹(AFP)可能源于多种潜在诊断。
这项回顾性研究旨在诊断2011年至2016年间转诊至儿科急诊专科单位的患有AFP的儿童。该研究收集了临床观察资料,进行了粪便和脑脊液分析,并评估了电生理和影像学数据。
本研究纳入了118名完全免疫接种的儿童,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)(6例)和疫苗相关麻痹性脊髓灰质炎(VAPP)(6例)。这6例患者均有原发性免疫缺陷。值得注意的是,所有患者的粪便分析中脊髓灰质炎病毒检测均为阴性。本研究遇到一例独特病例,一名2.5个月大的男性患者,表现为急性肢体运动无力,伴有发热、易激惹、新发肌张力减退和全身腱反射减弱。值得注意的是,未发现上运动神经元受累的迹象。脑脊液(CSF)分析与病毒性脑膜炎的诊断相符。此外,在进行的60例脑和脊髓影像学检查中,5例提示GBS,6例显示TMS证据,1例显示脊髓肿块。此外,临床调查表明,急性病毒性肌炎是本研究中20例患者AFP的次要病因。
在这项基于医院的研究中,三级儿科急诊室(ER)中因急性弛缓性麻痹AFP就诊的儿童最常见的诊断为GBS、急性病毒性肌炎、TMS和VAPP。这些发现表明,与基于社区的流行病学研究相比AFP的病因模式有所不同。此外,值得注意的是,诸如病毒性脑膜炎等不寻常情况很少表现出类似AFP的症状。对于VAPP病例,应考虑评估原发性免疫缺陷。最后,本研究实施了儿科AFP管理方案:一种本地实用方法。