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作 者:王颖超[1] 刘冬杰[1] 马丽娜[1] 刘满菊 盛光耀[1] 赵晓明[1]
机构地区:[1]郑州大学第一附属医院儿科/河南省高等学校临床医学重点学科开放实验室,河南郑州450052
出 处:《中国当代儿科杂志》2015年第1期26-30,共5页Chinese Journal of Contemporary Pediatrics
摘 要:目的探讨儿童噬血细胞综合征(HPS)与人微小病毒B19(HPVB19)感染可能存在的相关性,并对其临床特征进行分析。方法采用酶联免疫吸附试验(ELISA)和荧光定量PCR法对65例HPS患儿(HPS组)及65例健康体检儿童(对照组)进行HPVB19 Ig M、Ig G及HPVB19 DNA检测,并根据HPVB19DNA检测结果将HPS患儿分为HPVB19感染组(n=14)和非感染组(n=51),比较两组患儿临床资料。结果 HPS组HPVB19-Ig M阳性率(26%,17/65)显著高于对照组(9%,6/65)(P=0.011);而HPVB19-Ig G阳性率(38%,25/65)与对照组(29%,19/65)比较差异无统计学意义(P=0.266)。HPS组HPVB19感染率(22%,14/65)明显高于对照组(3%,2/65)(P=0.001)。与HPVB19非感染组HPS患儿比较,感染组患儿入院时血小板计数与血红蛋白水平显著降低,肝功能损伤更严重,发病时间更早,病程迁延时间更长(均P<0.05)。结论 HPVB19感染与HPS发病可能具有相关性。HPVB19感染的HPS患儿起病更急,临床表现更为严重,病程迁延时间更长。Objective To investigate the association of childhood hemophagocytic syndrome (HPS) with human parvovirus B19 (HPVB19) infection, and to analyze the clinical features of this disease. Methods ELISA and quantitative real-time PCR were used to detect HPVB19-IgM, HPVB19-IgG and HPVB19-DNA in 65 children with HPS (HPS group) and 65 healthy children (control group). The HPS group was divided into HPVB19-infected (n=14) and non-infected (n=51) groups according to the detection results of HPVB19-DNA. The clinical data of two groups were compared. Results The positive rate of HPVB19-IgM in the HPS group (26%, 17/65) was signiifcantly higher than that in the control group (9%, 6/65) (P=0.011), and there was no signiifcant difference in the positive rate of HPVB19-IgG between the HPS (38%, 25/65) and control groups (29%, 19/65) (P=0.266). The infection rate of HPVB19 in the HPS group (22%, 14/65) was signiifcantly higher than that in the control group (3%, 2/65) (P=0.001). Compared with the non-infected group, the HPVB19-infected group had signiifcantly lower platelet count and hemoglobin level on admission, signiifcantly more severe liver function damage, a signiifcantly earlier onset time, and a signiifcantly longer course of disease (P〈0.05). Conclusions The pathogenesis of HPS may be associated with HPVBl9 infection. HPVBl9-infected children with HPS have more acute onset, more severe clinical manifestations, and a longer disease duration.
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