Huang Ji-Qian, Ye Xiao-Hua, Yang Kang-Kang, Shangguan Yao-Yao, Dong Yi-Wei, Zheng Wen-Jie
Department of Pediatric Rheumatology, Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2021 Feb;23(2):143-147. doi: 10.7499/j.issn.1008-8830.2008097.
To study the clinical features of children with periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome, a polygenic and multifactorial autoinflammatory disease with unknown pathogenesis.
A retrospective analysis was performed on the medical data of 13 children with PFAPA syndrome.
All 13 children had disease onset within the age of 3 years, with a mean age of onset of (14±10) months. They all had periodic fever, with 8-18 attacks each year. The mean interictal period of fever was (30±5) days. Pharyngitis, cervical adenitis, and aphthous stomatitis were the three cardinal symptoms, with incidence rates of 100% (13/13), 85% (11/13), and 38% (5/13) respectively. There were increases in white blood cells, C-reactive protein, and erythrocyte sedimentation rate during fever. Of all the 13 children, 6 underwent whole exome sequencing and 7 underwent panel gene detection for autoinflammatory disease, and the results showed single heterozygous mutations in the gene in 6 children (46%). Recurrent fever in all children gradually returned to normal without antibiotics. Ten children were treated with a single dose of glucocorticoids, and fever was relieved after treatment. Of all the children, 4 were treated with cimetidine, among whom 2 had response; 4 children were treated with colchicine, among whom 2 had response and 2 were withdrawn from the drug due to adverse reactions. Tonsillectomy was performed for 2 children, among whom 1 was followed up for 3 years without recurrence and 1 still had recurrence.
For children with unexplained periodic fever with early onset accompanied by pharyngitis, cervical adenitis, aphthous stomatitis, elevated inflammatory indices, and good response to glucocorticoids, PFAPA syndrome should be considered. This disorder has good prognosis, and early diagnosis can avoid the long-term repeated use of antibiotics.
研究周期性发热、口疮性口炎、咽炎和腺炎(PFAPA)综合征患儿的临床特征,这是一种发病机制不明的多基因和多因素自身炎症性疾病。
对13例PFAPA综合征患儿的医疗数据进行回顾性分析。
13例患儿均在3岁内发病,平均发病年龄为(14±10)个月。均有周期性发热,每年发作8 - 18次。发热的平均间歇期为(30±5)天。咽炎、颈淋巴结炎和口疮性口炎为三大主要症状,发生率分别为100%(13/13)、85%(11/13)和38%(5/13)。发热时白细胞、C反应蛋白和红细胞沉降率升高。13例患儿中,6例进行了全外显子测序,7例进行了自身炎症性疾病的基因panel检测,结果显示6例患儿(46%)该基因存在单杂合突变。所有患儿的反复发热在未使用抗生素的情况下逐渐恢复正常。10例患儿接受单剂量糖皮质激素治疗,治疗后发热缓解。所有患儿中,4例使用西咪替丁治疗,其中2例有反应;4例使用秋水仙碱治疗,其中2例有反应,2例因不良反应停药。2例患儿行扁桃体切除术,其中1例随访3年无复发,1例仍有复发。
对于不明原因的早发性周期性发热,伴有咽炎、颈淋巴结炎、口疮性口炎、炎症指标升高且对糖皮质激素反应良好的患儿,应考虑PFAPA综合征。该疾病预后良好,早期诊断可避免长期反复使用抗生素。