Thalassemia and Hemoglobinopathy Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Neurosurgery, Central Clinical Hospital of the Ministry of the Interior and Administration, Warsaw, Poland.
Mol Biol Rep. 2022 Aug;49(8):8061-8069. doi: 10.1007/s11033-022-07352-x. Epub 2022 Mar 23.
As a recurrent disease, periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome is characterized by episodes of febrile attacks and is often prominent in children under five years of age. However, the etiology of this condition has not been fully understood yet.
The search in the extensive literature of peer-reviewed articles published from the inception to December 2021 was conducted to identify the relevant studies, using the electronic databases of MEDLINE/PubMed, Embase, Scopus, the Cochrane Library, and the Web of Science.
The analysis of complex relationships indicates that inflammatory factors, such as various cytokines and acute-phase proteins (APPs), play leading roles in the pathogenesis of this disease. Accordingly, this article summarizes the current state of knowledge to explain the mechanisms involved in inflammatory responses among patients with PFAPA syndrome and investigate its role in the pathogenesis of this disease. Moreover, the possibilities for further implementation of new therapeutic strategies are pointed out.
It is concluded that some pathophysiological processes are associated with immune dysregulation, which itself may be secondary to environmental factors, genetic background, and underlying diseases, including latent infections that multiply inflammatory mediators. elevated inflammatory markers similarly play a significant part in the clinical outcomes of this condition, whose pyrogenic nature is the reason for the development of episodes of febrile attacks in the population of patients suffering from PFAPA syndrome.
复发性周期性发热、口疮性口炎、咽炎和颈淋巴结炎(PFAPA)综合征是一种以发热性发作发作为特征的疾病,常发生于 5 岁以下儿童。然而,其病因尚未完全阐明。
通过检索 MEDLINE/PubMed、Embase、Scopus、Cochrane 图书馆和 Web of Science 等电子数据库,对截至 2021 年 12 月发表的同行评议文献进行广泛的文献检索,以确定相关研究。
对复杂关系的分析表明,炎症因子,如各种细胞因子和急性期蛋白(APPs),在该病的发病机制中起主导作用。因此,本文总结了目前的知识状况,以解释 PFAPA 综合征患者炎症反应的机制,并探讨其在该病发病机制中的作用。此外,还指出了进一步实施新治疗策略的可能性。
一些病理生理过程与免疫失调有关,而免疫失调本身可能继发于环境因素、遗传背景和潜在疾病,包括潜伏感染,这些因素会增加炎症介质。升高的炎症标志物同样在该病症的临床结果中起着重要作用,其发热性质是导致患有 PFAPA 综合征的患者发作发热性发作的原因。