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1)  congenital idiopathic haemolytic anemia
特发性溶血性贫血
1.
Methods Allo-PBSCTs were performed on 3 patients with β-thalassemia major and 1 patient with congenital idiopathic haemolytic anemia by the HLA-identical siblings donors or 1 locus-mismatch parent.
方法 用 HL A相合或不全相合的 Allo- PBSCT分别治疗重型β地中海贫血 3例 ,特发性溶血性贫血 1例。
2)  Hemolytic anemia
溶血性贫血
1.
Autoimmune hemolytic anemia associated with systemic lupus erythematosus;
系统性红斑狼疮合并自身免疫性溶血性贫血
2.
Systemic lupus erythematosus with hemolytic anemia as an initial symptom;
以溶血性贫血为首发表现的系统性红斑狼疮
3.
Case report complicated the autoimmune hemolytic anemia with both warm and cold autoantibodies and cryoglobulinemia in chronic lymphocytic leukemia and literature review;
慢性淋巴细胞白血病并发温冷双抗体型自身免疫性溶血性贫血和高冷球蛋白血症1例及文献复习
3)  acute hemolytic anemia
急性溶血性贫血
1.
Objective To explore the expression of human telmerase reverase transcriptase (hTERT) in bone marrow of children with acute hemolytic anemia and agranulocytosis,and the relationship between the expression of hTERT and hemoglobin level.
目的探讨急性溶血性贫血患儿人类骨髓端粒酶催化亚单位(hTERT)的表达及其与外周静脉血Hb水平的关系。
2.
OBJECTIVE To analyse the characteristics of acute hemolytic anemia induced by puerarin injection.
目的:分析葛根素注射液致急性溶血性贫血的特点。
3.
Objectives: To summarize key points for the diagnosis of hemolytic cirisis by analyzing clinical data of children with acute hemolytic anemia(AHA) and to explore the significances of both LDH and soluable transferritin receptor (sTfR) in the diagnosis of AHA.
目的:以临床分析为基础,总结急性溶血性贫血(简称急性溶贫)特别是溶血危象的特征,为“溶血危象”诊断提供临床依据;同时探讨血清乳酸脱氢酶(Iactic dehydrogenase,LDH)及可溶性血清转铁蛋白受体(soluable transferritin receptor,sTfR)在急性溶贫诊断中意义。
4)  chronic hemolytic anemia
慢性溶血性贫血
5)  hemolytic anemia
溶血性贫血症
6)  microangiopathic hemolytic anemia
微血管病性溶血性贫血
补充资料:伯氨喳啉型药物溶血性贫血


伯氨喳啉型药物溶血性贫血


  红细胞 6-磷酸葡萄糖脱氢酶(G-6-PD)缺乏的特异质患者,由于服用伯氨喹啉型药物可诱发溶血性贫血。这是一种遗传性生化缺陷。由于G-6-PD缺乏,使*还原型辅酶Ⅱ(NADPH)生成减少。导致红细胞内还原型谷胱甘肽(GSH)缺乏,使红细胞失去了GSH的保护作用,就易遭受伯氨喹啉的代谢产物6-羟基衍化物的氧化,造成溶血现象,并可出现高铁血红蛋白血症。因此,临床除表现溶血症状外,还可出现紫绀。防治:停服诱发溶血的药物,输液、输血,并加用Vit.E;对已明确G-6-PD缺乏的患者应告知注意事项。
  
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