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红细胞增多

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Hemolysis can be caused by fetal anemia, cardiomegaly, liver, splenomegaly, edema of the fetus and placenta, blood erythrocytosis, severe fetal hypoxia, resulting in intrauterine fetal death.

溶血可致胎儿贫血、心脏扩大,肝、脾肿大,胎儿及胎盘水肿,血液中红细胞增多,严重时胎儿缺氧,造成胎死宫内。

All patients presented at a young age with elevated serum Epo. Mutations at Gly-537 account for 4 of 5 HIF2A mutations associated with erythrocytosis.

所有病人在年轻时血清红细胞生成素较高,5个与红细胞增多症相关的HIF2A突变有4个是在Gly-537发生突变。

Features of the related myeloproliferative disorder included isolated erythrocytosis, distinctive bone marrow morphology, and reduced serum erythropoietin levels.

相关骨髓增生碍的主要特征为:独立的红细胞增多,特征性的骨髓心态学以及血清中促红细胞生成素的减少。

Erythrocytosis can arise from deregulation of the erythropoietin axis resulting from defects in the oxygen-sensing pathway.

缺氧信号传导途径的缺陷导致的红细胞生成素轴调控异常会引起红细胞增多症的发生。

It is with printing and section contrast, 124 smear have nuclear cell to decrease in, 58.9% decrease with the 66.1% positive that it is a holiday, common by accident for; of bring down of aplastic anemia, hematopoiesis printing and section cell quantity increase examine disease in, smear still has 26% decrease with the 36% negative that it is a holiday, common disease or conclusion are grow in quantity of red blood cell of lienal function hyperfunction, true sex disease, special the; such as disease of grow in quantity of the plaque that send a gender printing and section cell bring down person in, smear is accorded with rate (91.2% with 97.9%), and in the person that smear cell increases, printing and section are accorded with rate (95% with 100%) all tall.

以印片和切片为对照,124例涂片有核细胞减少中,58.9%和66.1%为假阳性减少,常见误诊疾病为再生障碍性贫血、造血减低;而印片和切片细胞量增加中,涂片仍有26%和36%为假阴性减少,常见疾病或结论为脾功能亢进、真性红细胞增多症、特发性血小板增多症等;印片和切片细胞减低者中,涂片符合率(91.2%和97.9%),以及涂片细胞增加者中,印片和切片符合率(95%和100%)均高。

ObjectiveThe monge disease is chronic plateau sickness and common disease.This article is to discuss the clinical observation and nursing on monge disease.

目的 高原性红细胞增症是慢性高原病中的常见病本文探讨我院内科红细胞增多症患者的临床观察和护理。

Of myeloproliferative diseases which include 61 of polycythemia vera, 43 of essential thrombocythemia and 11 of primary myelofibrosis cases were tested and analyzed.

对115例MPD患者进行检测,包括61例真性红细胞增多症患者、43例原发性血小板增多症患者和11例原发性骨髓纤维化患者。

Abstract] AIM: To study the relationship between erythrocyte rheological properties and lipid peroxidation in patients with high altitude polycythemia.

研究表明,在低氧环境下,%26127;红细胞变形能力降低是导致高原红细胞增多症(high altitude polycythemia,HAPC)病理生理异常改变的主要原因之一[1]。

It was found that the membrane shear elastic modulus and membrane viscosity decreased in this process of changing. This finding may have some basic theoretical and clinical significance.

这对研究由于贫血等原因造成的网织红细胞增多情况下全血的微观流变学特性有重要的临床意义,同时对新生网织红细胞在转化过程中膜的剪切弹性模量和表面粘度的变化规律加以系统研究,具有重要的基础理论研究价值。

Smear diagnostic cell measures true sex to reduce disease or verdict (aplastic anemia and hematopoiesis bring down) false positive is respectively 29.0% with 37.1%, diagnose true sex to increase a disease (lienal function hyperfunction, special disease of disease of grow in quantity of the plaque that send a gender, grow in quantity of true sex red blood cell) false negative rate is 22.6% with 21.8%, diagnostic index performance is evaluated all not beautiful.

涂片诊断细胞量真性减少疾病或结论(再生障碍性贫血和造血减低)的假阳性分别为29.0%和37.1%,诊断真性增加疾病(脾功能亢进、特发性血小板增多症、真性红细胞增多症等)假阴性率为22.6%和21.8%,诊断指标性能评价均不佳。

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