Division of Pediatric Allergy and Asthma Unit, Department of Pediatrics, Faculty of Medicine, Hacettepe University, 06410, Sıhhiye, Ankara, Turkey.
Division of Pediatric Immunology, Department of Pediatrics, Faculty of Medicine, Hacettepe University, 06410, Sıhhiye, Ankara, Turkey.
Eur J Pediatr. 2023 Jun;182(6):2833-2842. doi: 10.1007/s00431-023-04961-x. Epub 2023 Apr 12.
Eosinophilia is common in children and may be caused by various disorders. Large-cohort studies, including mild cases, are limited in children. This study aimed to reveal underlying etiologies of childhood eosinophilia and to create a diagnostic algorithm. Children (< 18 years) with absolute eosinophil counts (AECs) ≥ 0.5 × 10/L were reviewed from medical files. Clinical characteristics and laboratory values were recorded. Patients were grouped based on the severity of eosinophilia as mild (0.5-1.5 × 10/L), moderate (≥ 1.5 × 10/L) and severe (≥ 5.0 × 10/L). An algorithm was formed to evaluate these patients. We included 1178 children with mild (80.8%), moderate (17.8%) and severe eosinophilia (1.4%). The most common reasons of eosinophilia were allergic diseases (80%), primary immunodeficiency (PID) (8.5%), infectious diseases (5.8%), malignancies (0.8%) and rheumatic diseases (0.7%). Only 0.3% of children presented with idiopatic hypereosinophilic syndrome. Allergic diseases and PIDs were the most common etiologies in mild/moderate and severe groups, respectively. The median duration of eosinophilia was 7.0 (3.0-17.0) months in the study population and was the shortest in severe cases (2.0 (2.0-5.0) months). Multiple logistic regression analysis demonstrated food allergy [OR:1.866, 95%CI:1.225-2.842, p = 0.004] and PIDs [OR:2.200, 95%CI:1.213-3.992, p = 0.009] as independent factors for childhood eosinophilia. A diagnostic algorithm including mild form was presented for childhood eosinophilia. Conclusion: Eosinophilia was frequently determined due to secondary causes; allergic diseases in mild/moderate eosinophilia, PIDs in severe group. Etiology of eosinophilia was diverse, and an algorithm concerning the severity of eosinophilia would be practical and rational. What is Known: • In children, eosinophilia is common, and mild eosinophilia occurs frequently. • Malignancies presents frequently with severe eosinophilia. What is New: • Primary immunodeficiencies were not a rare cause of eosinophilia, especially in countries such as the Middle East and eastern Mediterranean countries, where the countries consanguineous marriages are common, and should be investigated in children with eosinophilia who do not have allergic or infectious diseases. • In literature, there are many algorithms about childhood hypereosinophilia. However, mild eosinophilia is extremely important in children. Because all patients with malignancy and most of the patients with rheumatic diseases presented with mild eosinophilia. Therefore, we proposed an algorithm for childhood eosinophilia that includes mild eosinophilia besides moderate and severe cases.
嗜酸性粒细胞增多症在儿童中很常见,可能由各种疾病引起。包括轻度病例在内的大型队列研究在儿童中受到限制。本研究旨在揭示儿童嗜酸性粒细胞增多症的潜在病因,并制定诊断算法。从病历中回顾了嗜酸性粒细胞绝对计数(AEC)≥ 0.5×10/L 的儿童。记录了临床特征和实验室值。根据嗜酸性粒细胞增多的严重程度将患者分为轻度(0.5-1.5×10/L)、中度(≥1.5×10/L)和重度(≥5.0×10/L)组。制定了一个评估这些患者的算法。我们纳入了 1178 名嗜酸性粒细胞轻度(80.8%)、中度(17.8%)和重度(1.4%)的儿童。嗜酸性粒细胞增多最常见的原因是过敏疾病(80%)、原发性免疫缺陷(PID)(8.5%)、传染病(5.8%)、恶性肿瘤(0.8%)和风湿性疾病(0.7%)。只有 0.3%的儿童出现特发性嗜酸性粒细胞增多症。过敏疾病和 PID 是轻度/中度和重度组中最常见的病因。研究人群中嗜酸性粒细胞增多的中位持续时间为 7.0(3.0-17.0)个月,在重度病例中最短(2.0(2.0-5.0)个月)。多变量逻辑回归分析表明,食物过敏[OR:1.866,95%CI:1.225-2.842,p=0.004]和 PID[OR:2.200,95%CI:1.213-3.992,p=0.009]是儿童嗜酸性粒细胞增多的独立因素。提出了一个包括轻度形式的儿童嗜酸性粒细胞增多症的诊断算法。结论:嗜酸性粒细胞增多症常继发于其他原因;轻度/中度嗜酸性粒细胞增多症为过敏疾病,重度组为 PID。嗜酸性粒细胞增多症的病因多种多样,关于嗜酸性粒细胞增多严重程度的算法将是实用和合理的。已知情况:儿童嗜酸性粒细胞增多症常见,轻度嗜酸性粒细胞增多症常见。恶性肿瘤常伴有重度嗜酸性粒细胞增多。新情况:原发性免疫缺陷不是嗜酸性粒细胞增多症的罕见原因,尤其是在中东和东地中海国家等近亲婚配常见的国家,应在无过敏或感染性疾病的嗜酸性粒细胞增多症患儿中进行调查。文献中有许多关于儿童嗜酸性粒细胞增多症的算法。然而,轻度嗜酸性粒细胞增多症在儿童中非常重要。因为所有患有恶性肿瘤的患者和大多数患有风湿性疾病的患者都表现为轻度嗜酸性粒细胞增多症。因此,我们提出了一个包括轻度、中度和重度嗜酸性粒细胞增多症的儿童嗜酸性粒细胞增多症算法。