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溶血性疾病中的双重杂合因素及溶血系统分析的临床意义(附506例贫血黄疸病因分析) 被引量:6

Compound heterozygote factor and clinical significance of hemolysis system analysis in the diagnosis of congenital hemolytic anemia:Etiological analysis of 506 cases of anemia and jaundice
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摘要 目的:分析初诊为贫血或溶血患者的发病原因。方法:常规筛查506例贫血、黄疸溶血、脾大患者,经试验确定存在溶血后,针对性进行血红蛋白病、红细胞膜病、红细胞酶病和后天获得性溶血指标系统分析及家系调查。结果:506例患者中,确诊病因的溶血性疾病384例,病因不明的溶血性贫血21例,非溶血性血液病33例,非血液疾病24例,失访44例。在病因明确的384例溶血性疾病中,遗传性溶血病因356例,其他溶血病因28例。遗传性溶贫中血红蛋白病114例、红细胞膜病133例、红细胞酶病65例、双重杂合子44例。将双重杂合子中的各个病因出现次数与前3大类病因组合并,则先天溶贫病因百分比分别为血红蛋白病34.62%、红细胞膜病42.56%、红细胞酶病22.82%。红细胞缺陷酶的比例为葡萄糖-6-磷酸脱氢酶41.57%、丙酮酸激酶44.94%、嘧啶-5'核苷酸酶3.37%、磷酸果糖激酶3.37%、NADH-高铁血红蛋白还原酶4.49%、醛缩酶1.12%、谷胱甘肽还原酶1.12%。结论:双重杂合子红细胞存在两种遗传缺陷,易互相干扰诊断提示。溶血系统分析和家系调查可以提高溶血性贫血病因确诊率,尤其对红细胞酶病和双重杂合子具有鉴别诊断意义。 Objective:To analyze the etiology of 506 cases of anemia and jaundice. Method:On the basis of hemolytic screen tests confirming the existence of hemolysis, system analysis and family survey of hemoglobinopathy, erythrocyte membranopathy, erythrocyte enzymopathy and acquired hemolytic diseases were carried out. Result:Of the 506 cases, cause-confirmed hemolytic diseases were 384 cases, unknown-cause hemolytic diseases 21 cases, nonhemolytic hematologic diseases 33 cases, non-hematologic diseases 24 cases and follow-up-missing 44 cases. In the 384 cause-confirmed hemolytic cases, heredity hemolysis were 356, of whom hemoglobinopathy was 114, membranopathy 133, enzymopathy 65 and compound heterozygote 44 (12.36%). Combining the etiological factors with compound heterozygotes, the total percentage of hemoglobinopathy was 34.62%, membranopathy 42.56% and enzymopathy 22.82%. Of erythrocyte defected enzymes, glucose-6-phosphate dehydrogenase were 41.57%, pyruvate kinase 44.94%, pyrimidine 5'-nucleotidase 3.37%, phosphofructokinase 3.37%, NADH-Diaphorase 4.49%, aldolase 1.12%, glutathione reductase 1.12%. Conclusion:The diagnostic clues of double heterozygote could be interferenced by two kinds of abnormalities in erythrocyte. Hemolytic systemic analysis and family survey may improve the etiologically differential diagnosis of hemolytic anemia especially for enzymopathy and double heterozygote.
出处 《临床血液学杂志》 CAS 2005年第4期204-206,共3页 Journal of Clinical Hematology
关键词 贫血 溶血性 双重杂合子 系统分析 家系调查 Hemolytic anemia Double heterozygote Systemic analysis Family survey
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  • 1[1]Walensky LD,Shi ZT,Blackshaw S,et al.Neurobehavioral deficits in mice lacking the erythrocyte membrane cytoskeletal protein 4.1[J].Curr Biol,1998,8(23):1269-1272.
  • 2[2]Gallagher PG,Forget BG.The red cell membrane[A]. In: Beutler E, et al ed.Wiliams hematology[M].6th ed.北京:人民卫生出版社,2001.333-343.
  • 3李津婴,万树栋.戊二醛固定液用于红细胞形态观察[J].中华血液学杂志,1992,13(6):317.
  • 4[4]Gimm JA,An X,Nunomura W,Mohandas N.Functional characterization of spectrin-actin-binding domains in 4.1 family of proteins[J]. Biochemistry, 2002,41(23):7275-7282.
  • 5[5]Denker SP,Barber DL.Ion transport proteins anchor and regulate the cytoskeleton[J].Curr Opin Cell Biol,2002,14(2):214-220.
  • 6[7]Gallagher PG,Forget BG.Hereditary spherocytosis,elliptocytosis,and related disorders[A]. In: Beutler E, et al ed.Wiliams hematology[M].6th ed.北京:人民卫生出版社,2001.503-518.
  • 7[8]Yawata Y,Kanzaki A,Yawata A,et al.Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population[J].Int J Hematol,2000,71(2):118-135.

共引文献14

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  • 1邓燕艺,张华,李梅,刘勇,卢桂森.广西遗传性球形红细胞增多症一个家系调查[J].中国优生与遗传杂志,2005,13(3):120-120. 被引量:2
  • 2Stasiuk M,Kijanka G,Kozubek A.Transformations of erythrocytes shape and its regulation[J].Postepy Biochem,2009,55(4):425-433.
  • 3Guitton C,Garcon L,Cynober T,et al.Hereditary spherocytosis:guidelines for the diagnosis and management in children[J].Arch Pediatr,2009,16(6):556-558.
  • 4Bolton-Maggs PH,Stevens RF,Dodd NJ,et al.Guidelines for the diagnosis and management of hereditary spherocytosis[J].Br J Haematol,2004,126(4):455-474.
  • 5Radhakrishnan K,Tan C,Gallo J.Erythrophagocytosis in hemolytic disease of the newborn[J].Am J Hematol,2008,83(8):679.
  • 6Mamtani M,Sharma M,Amin M,et al.Erythrophagocytosis in sickle cell anemia:statistical evidence for a biological phenomenon[J].Med Hypotheses,2007,68 (5):1065-1070.
  • 7Islam MS,Chia L.Hyperhemolysis syndrome in a patient with sickle cell disease with erythrophagocytosis in peripheral blood[J].Eur J Haematol,2010,84(2):188.
  • 8Fendel R,Brandts C,Rudat A,et al.Hemolysis is associated with low reticulocyte production index and predicts blood transfusion in severe malarial anemia[J].PLoS One,2010,5(4):e10038.
  • 9An X,Mohandas N.Disorders of red cell membrane[J].Br J Haematol,2008,141 (3):367-375.
  • 10Tavazzi D,Taher A,Cappellini MD.Red blood cell enzyme disorders:an overview[J].Pediatr Ann,2008,37(5):303-310.

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