Pediatric Allergy and Immunology Unit, Children's Hospital, 68903Ain Shams University, Egypt.
Pediatric Nephrology Unit, Children's Hospital, 68903Ain Shams University, Egypt.
Sci Prog. 2021 Jul-Sep;104(3):368504211044042. doi: 10.1177/00368504211044042.
We sought to screen for clinical and laboratory features of hemophagocytic lymphohistiocytosis among pediatric patients with severe sepsis.
We conducted a retrospective study that analyzed the clinical and laboratory data of 70 pediatric patients who died of severe sepsis. Medical records were revised for the presence of fever, splenomegaly, pancytopenia, hyperferritinemia, hypertriglyceridemia, and hypofibrinogenemia. Soluble CD25 was measured in stored samples.
Patients' ages ranged between 0.5 and 11 years with median (interquartile range) 2 (1-5). All patients had fever (≥38.5 °C) and pancytopenia, 58 (82.9%) hepatosplenomegaly, 36 (51.4%) lymphadenopathy, 37 (52.9%) had ferritin >500 ng/ml, 20 (28.6%) had fibrinogen <1.5 mg/ml, 14 (20%) had fasting triglycerides >264 mg/dl while 5 (7.1%) had soluble CD25 >2400 U/ml. Twenty-five (35.7%) patients fulfilled at least 5/6 of the hemophagocytic lymphohistiocytosis-2004 diagnostic criteria. Multivariate backward binary logistic regression analysis revealed lymphadenopathy as an independent predictor for hemophagocytic lymphohistiocytosis criteria fulfilment with odds ratio of 23.9. Fibrinogen had the best performance in discriminating hemophagocytic lymphohistiocytosis fulfilling from non-fulfilling groups (cut-off value: <1.8 mg/ml), followed by ferritin/erythrocyte sedimentation rate ratio (cut-off value: >17).
There is a significant clinical and laboratory overlap between hemophagocytic lymphohistiocytosis and severe sepsis, making the syndromes difficult to distinguish. The use of current hemophagocytic lymphohistiocytosis-2004 diagnostic criteria should be applied cautiously in those patients.
我们试图在患有严重脓毒症的儿科患者中筛选噬血细胞性淋巴组织细胞增生症的临床和实验室特征。
我们进行了一项回顾性研究,分析了 70 名死于严重脓毒症的儿科患者的临床和实验室数据。修订了病历以确定发热、脾肿大、全血细胞减少、高铁蛋白血症、高三酰甘油血症和低纤维蛋白原血症的存在。在储存的样本中测量可溶性 CD25。
患者年龄在 0.5 至 11 岁之间,中位数(四分位距)为 2(1-5)。所有患者均有发热(≥38.5℃)和全血细胞减少,58 例(82.9%)肝脾肿大,36 例(51.4%)淋巴结病,37 例(52.9%)铁蛋白>500ng/ml,20 例(28.6%)纤维蛋白原<1.5mg/ml,14 例(20%)空腹甘油三酯>264mg/dl,5 例(7.1%)可溶性 CD25>2400U/ml。25 例(35.7%)患者至少满足噬血细胞性淋巴组织细胞增生症-2004 诊断标准的 5/6 项。多变量向后二元逻辑回归分析显示,淋巴结病是满足噬血细胞性淋巴组织细胞增生症标准的独立预测因子,优势比为 23.9。纤维蛋白原在区分满足和不满足噬血细胞性淋巴组织细胞增生症标准的组方面表现最佳(临界值:<1.8mg/ml),其次是铁蛋白/红细胞沉降率比值(临界值:>17)。
噬血细胞性淋巴组织细胞增生症和严重脓毒症之间存在显著的临床和实验室重叠,使这些综合征难以区分。在这些患者中,应谨慎使用现行的噬血细胞性淋巴组织细胞增生症-2004 诊断标准。