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1.
为了解小儿感染性疾病红细胞内锌原卟淋(ZPP)值及其临床。方法:对61例小儿感染性疾病进行ZPP及血红蛋白(Hb),红细胞计数(RBC)及平均红细胞体积(MCV)的测定,以健康体检儿童作为对照,结果: 感染组儿童ZPP值明显高于对照组(P<0.05),Hb、MCV值明显低于对照组(P<0.05),RBC值无明显差异(P<0.05)。不同性别之间ZPP、Hb、RBC、MCV值无统计学差异(P<0.05)。肺炎、肺结核、肠炎的ZPP值较上呼吸道感染及皮肤感染患儿高,败血症患儿ZPP值最高,Hb、RBC、MCV值较低,但无统计学差异(P<0.05)。结论:小儿感染性疾病存在铁代谢紊乱。应用ZPP筛查铁缺乏症时,应避免感染因素的干扰,ZPP也可作为儿童感染及感染严重程度的观察指标。  相似文献   

2.
近年来的研究表明,锌原卟啉除了可以作为评价铁营养状况和辅助诊断铅中毒的重要实验指标外,还通过抑制血红素氧化酶的活性,参与血红蛋白的分解代谢,在控制新生儿胆红素形成,预防高胆红素血症方面具有潜在的治疗作用。本文主要介绍其基础研究方法和临床应用的研究进展。  相似文献   

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西宁市3—12岁儿童Hb—SFEP测定值的相关分析   总被引:1,自引:0,他引:1  
本文通过要市426名3 ̄12岁儿童Hb及FEP二项值的测定,发现用全国建议的西它折算标准来判断本组儿童的贫血患病率为51.70%,其中非缺铁性贫血竞高达44.4%。因此,建议为解决我国不同海拔高度地区血红蛋白低限值的标准制定,必须对所测样本作出严格的统一要求。  相似文献   

4.
铅污染区儿童血铅与锌原卟啉、红细胞参数相关性研究   总被引:3,自引:0,他引:3  
目的 探讨铅污染区儿童血铅与锌原卟啉、红细胞参数相关性。方法 对云南某县铅锌矿区和县城非铅锌矿区2~9岁儿童共464人进行血铅(BPb)水平、红细胞参数及锌原卟啉(ZPP)水平调查,按血铅水平分为高、低血铅组并进行血Pb与红细胞参数(RBC、HB、HCT、MCV、MCH、MCHC、RDW)及ZPP相关性分析。结果儿童血铅浓度均值154.4ug/L,铅中毒率79.1%,ZPP均值2.7ug/gHb。血铅〉250ug/L时,血铅与红细胞参数具有相关性(RR:0.637)。高铅组血铅水平与RBC、ZPP有较强相关性(r分别为:-0.975、0.957)。RBC随血铅水平增高呈高度负相关,血铅水平〈200ug/L时,与zPP无相关性。血铅水平达~250ug/L、~300u∥L、~350ug/L时,血铅与ZPP具有较强相关性(r分别为:0.567、0.93、0.886)并呈高度正相关。结论随血铅水平的增高,RBC与血铅呈高度负相关,当血铅水平〉250ug/L时,血铅与ZPP具有高度正相关性,而当血铅水平〈200ug/L时,与ZPP相关关系不密切,因此ZPP不能作为铅中毒筛查指标。  相似文献   

5.
目的探讨铅污染区儿童血铅与锌原卟啉、红细胞参数相关性。方法对云南某县铅锌矿区和县城非铅锌矿区2~9岁儿童共464人进行血铅(BPb)水平、红细胞参数及锌原卟啉(ZPP)水平调查,按血铅水平分为高、低血铅组并进行血Pb与红细胞参数(RBC、HB、HCT、MCV、MCH、MCHC、RDW)及ZPP相关性分析。结果儿童血铅浓度均值154.4ugL,铅中毒率79.1%,ZPP均值2.7uggHb。血铅>250ugL时,血铅与红细胞参数具有相关性(RR:0.637)。高铅组血铅水平与RBC、ZPP有较强相关性(r分别为:-0.975、0.957)。RBC随血铅水平增高呈高度负相关,血铅水平<200ugL时,与ZPP无相关性。血铅水平达~250ugL、~300ugL、~350ugL时,血铅与ZPP具有较强相关性(r分别为:0.567、0.93、0.886)并呈高度正相关。结论随血铅水平的增高,RBC与血铅呈高度负相关,当血铅水平>250ugL时,血铅与ZPP具有高度正相关性,而当血铅水平<200ugL时,与ZPP相关关系不密切,因此ZPP不能作为铅中毒筛查指标。  相似文献   

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血锌原卟啉对缺铁性贫血早期诊断及疗效观察的临床意义   总被引:2,自引:0,他引:2  
研究目的探讨血锌原卟啉(Zpp)测定对小儿缺铁性贫血早期诊断及疗效的临床意义。研究方法铁缺乏患儿232例(140例伴贫血,92例为非贫血铁缺乏),80例正常儿童为对照组,进行血Zpp测定研究。并对20例血清铁蛋白正常的贫血患儿进行铁试验治疗。结果缺铁性贫血组及非贫血缺铁组的Zpp值(分别为1.423±0.253μmol/L及1.040±0.133μmol/L)均明显高于对照组(0.566±0.121μmol/L)(P<0.01)。铁试验治疗显示,随治疗的继续,Zpp值逐渐下降,治疗8周后Zpp下降正常,贫血纠正。结论Zpp作为缺铁性贫血早期诊断及疗效观察的指标,具有很大的临床价值。  相似文献   

8.
目的 探讨感染性疾病患儿血清降钙素原(PCT)、前清蛋白(PA)和CRP测定的临床意义.方法 感染儿童78例被分为细菌感染组(35例)与病毒感染组(43例).2组患儿均检测血清PCT、CRP和PA水平,并与35例年龄、性别相匹配的健康儿童各检测值进行比较.结果 1.以血清PCT≥0.5μg/L为阳性标准,细菌感染组PCT阳性率为80%(28/35例),病毒感染组为18.6%(8/43例);以血清CRP≥8 mg/L为阳性标准,细菌感染组CRP阳性率为68.6%(24/35例),病毒感染组为23.2%(10/43例).2.与健康对照组比较,细菌感染组PCT、CRP均明显升高(Pa<0.01),PA明显降低(P<0.01);细菌感染组PCT、CRP均高于病毒感染组(Pa <0.05),PA明显低于病毒感染组(P<0.01).结论 PCT、PA和CRP的检测对于细菌性感染和病毒性感染的鉴别诊断有一定价值.  相似文献   

9.
反复呼吸道感染儿红细胞免疫粘附功能及锌治疗   总被引:6,自引:0,他引:6  
反复呼吸道感染儿红细胞免疫粘附功能及锌治疗(杭州市第一医院310006)何内华,张锦铭,张玉芳反复呼吸道感染儿童的低免疫状态,常使临床抗感染治疗变得颇为棘手。80年代后随着人类对红细胞免疫粘附(RCIA)功能的发现与认识,对疾病的免疫病理机制又有了新...  相似文献   

10.
反复呼吸道感染(RRI)是儿科常见病,发病率在20%以上。目前已公认免疫力低下是其主要致病因素,临床中发现小剂量补充锌剂能改善儿童的锌营养状况及免疫功能[1]。我们通过对42例低锌水平RRI患儿的红细胞锌及T细胞亚群进行动态观察、对照比较,以期进一步了解小剂量锌剂补充对RRI发病的干预机理与疗效。资料与方法一、对象按1987年全国小儿呼吸道会议制定的标准确诊为RRI患儿42例,年龄1~7岁,全部普查血清锌,低于正常水平11.47μmol/L者,按随机分配原则分为补锌组26例(男14例、女12例)及对照组16例(男9例、女7例)。二、方法补锌组采取常规…  相似文献   

11.
为探讨小儿急性白血病 (AL)多药耐药基因MDR1表达的临床价值 ,检测2 8例AL患者 4 8份标本的MDR1基因 ,并对其中 2 0例患儿进行了动态观察。结果 ,小儿急性白血病在治疗的不同阶段其MDR1的阳性率不同 :化疗前的阳性率为 2 5 % ,MDR1阳性与MDR1阴性患者的完全缓解率 (CR)分别为 33%和 92 % (P <0 .0 1) ,耐药组的阳性率为 80 % ,而非耐药组的阳性率为 16 % (P <0 .0 1)。复发组的MDR1阳性率为 75 % ,而持续缓解组的MDR1阳性率为 16 % (P <0 .0 5 )。正常人MDR1阳性率为零。结果表明检测MDR1对判断化疗效果和估计预后均有很重要的作用 ,同时可为临床合理选择化疗方案提供一个客观指标  相似文献   

12.
300 consecutive children admitted to hospital with infectious hepatitis were followed up until they had‘recovered’. One month after leaving hospital only 28% were fully recovered; the remainder still showed relevant symptoms and/or signs and/or biochemical abnormality. Symptoms and signs resolved quickly but abnormal levels of serum glutamic pyruvic transaminase persisted for up to 6 months, and an abnormal reaction to the zinc sulphate turbidity test (ZSTT) for much longer.  相似文献   

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为了探讨热应激蛋白(HSPs)与白血病化疗及分类的关系,应用Western斑点、印迹方法,检测了54例白血病患儿71份脑脊液HSP90、70、60、27水平。结果:(1)化疗后骨髓缓解期HSP90、7O、6O、27均明显高于危象期(P<0.01和P<0.05);(2)与非肿瘤组对比危象期HSP70、60、明显降低(P<0.01),缓解期HSP90、27明显增高(PMO.01);(3)从双份标本结果发现,HSPS总体水平由低向高发展预后好,而持续低水平或由高向低发展预后差;(4)急性淋巴细胞性白血病患JLHSP70、6O明显高于急性非淋巴细胞性白血病。提示:HSPS参与白血病的免疫防护,与白血病的分类有密切关系。HSPS水平的测定对指导白血病治疗及预后的评价具有重要意义。  相似文献   

16.
Immunosuppressive therapy (6-Mercaptopurine) has been used in 33 children with chronic renal diseases resistant to other therapeutic methods. Peripheral blood counts were done in all the children and in 18 of them bone marrow examinations were performed. The results of immunosuppressive therapy were encouraging; many compleie and partial remissions being obtained. Children with nephrotic syndrome showed low percentages of erythroblasts in bone marrow. This was not observed in children suffering from chronic glomerulo- and pyelonephritis. Immunosuppressive therapy provoked increase of erythroblasts in bone marrow of children with nephrotic syndrome.  相似文献   

17.
THE GROWTH OF THE KIDNEYS IN CHILDREN WITH VESICOURETERIC REFLUX   总被引:1,自引:0,他引:1  
Abstract. In a retrospective study, 69 kidneys with VUR were divided into 2 groups: One group (A) where VUR stopped within 1 year after operation or conservative treatment and a second group (B) where VUR continued for more than 1 year. Group A had somewhat more severe grades of reflux than group B. The number of infections were practically the same in the two groups. The length of the kidneys was measured at the time of diagnosis and compared with the length at the most recent urography after VUR stopped (group A) on average 2 years and 3 months later and with the most recent urography while VUR was still present (group B) on average 1 year and 9 months later. It was found that 85% in group A had increased in absolute length while the figure was 60% in group B. If the relative growth is calculated (the kidneys' length in relationship to L1 - L3 distance), 60% in group B had decreased while only 30% in group A had decreased.  相似文献   

18.
人细小病毒B19(HumanParvovirrusB19,HPVB19)与人类多种疾病密切相关,可通过接触和使用血液制品等在人群中传播[1],本文采用聚合酶链反应(PCR)技术检测45例血液病患儿血清HPVB19-DNA,结果总阳性率为26.6%,其中急性白血病占38.8%(7/18),ITP占40.0%(4/10),过敏性紫癜占8.3%(1/12),再障5例均为阴性;同时检测对照组10名正常儿童均为阴性。将病例组与对照组进行比较有显著意义(P<0.05)。  相似文献   

19.
Loss of chromosome 7 material, either as complete loss of one chromosome-monosomy 7 (-7)- or as deletion of the long arm (7q-), is the most common cytogenetic abnormality in childhood myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML), seen in approximately 30% of the cases. Only 4-5% of childhood acute myeloid leukemia (AML) cases show -7/7q-. Monosomy 7 in children has often been considered to represent a distinct hematologic disorder described as the monosomy 7 syndrome. Loss of chromosome 7 occurs in a heterogeneous group of myeloid disorders and recent data give no support to the concept of monosomy 7 as a distinct syndrome. Only patients with a diagnosis of JMML fit what previously has been referred to as the monosomy 7 syndrome. There are no major clinical differences between JMML with and without -7. Unlike what has been found in adults, monosomy 7 is not a poor prognostic factor in childhood MDS. However, -7 in AML is associated with a very poor prognosis. AML with 7q-, in contrast, has an outcome similar to AML with normal karyotype. Stem cell transplantation is the treatment of choice and should be performed as early as possible.  相似文献   

20.
本文应用放射配体结合法测定了30例ALL骨髓细胞GCR为7873±3002位点/细胞;17例ANLL为6113±1622位点/细胞(P<0.05)。形态学分型L1型17例,GCR为7267±3178位点/细胞;L2型13例,GCR为7650±3362位点/细胞(P>0.05)。临床分型标危型ALL14例,GCR为8998±1963位点/细胞;高危型9例为5847±3885位点/细胞(P<0.05)。对18例ALL经联合化疗完全缓解前后比较发现,GCR分别为8115±3258位/细胞和4669±2106位点/细胞(P<0.01)。本实验同时测定了ALL和ANLL患儿血浆皮质醇浓度,平均分别为112.20±41.14ng/mi和104.65±43.49ng/ml,相关系数分别为r=0.15和0.11,说明GCR表达水平不受皮质醇含量的影响。  相似文献   

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