这是极少见的遗传性球形红细胞增多症。
There is a rare condition known as hereditary spherocytosis.
如真性红细胞增多症。
目的分析儿童遗传性球形红细胞增多症的临床特点。
Objective to analyze the clinical feature of children hereditary spherocytosis (HS).
目的探讨胎儿有核红细胞增多症胎盘的临床病理意义。
Objective: to study the clinicopathological significance of fetal nucleated erythrocytosis placenta.
本文24例红细胞增多症以围产期因素引起者占首位。
Fhis paper reports 24 newborns with erythrocythemia caused mainly by perinatal factors.
目的：探讨EPO在高原红细胞增多症发病机制中的作用。
Objective: To investigate the role of EPO in the pathogenesis of high altitude polycythemia (HAPC).
OSAS组的高血压和继发性红细胞增多症明显高于对照组。
There were more patients complicated with hypertension and secondary polycythemia inOSAS group than in control group.
目的探讨高原红细胞增多症(HAPC)患者鼻出血的临床特点。
Objective To characterize clinical feature of rhinorrhagia correlated with high altitude polycythemia (HAPC).
血液病患者，如贫血、白血病、真性红细胞增多症及各种出、凝血性疾病。
Blood, such as anemia, leukemia patients increased erythrocyte healthily, disease and various diseases, and clotting hemorrhagic.
新生儿低出生体质量、呼吸窘迫综合征及红细胞增多症是THP的危险因素。
Neonatal low birth weights, respiratory distress syndrome and polycythemia are risk factors for THP.
目的分析遗传性球形红细胞增多症(HS)误诊、漏诊原因，以提高其诊断率。
Objective to analyze the causes of misdiagnosis and missed diagnosis in hereditary spherocytosis (HS) and improve the diagnosis rate.
白血病动物虽然在骨髓充满原始红细胞却依然贫血，而真性红细胞增多症真的有很多红细胞。
Animals with erythroleukemia are anemic despite having a marrow filled with rubriblasts, where as those with polycythemia vera have erythrocytosis.
目的探讨高原红细胞增多症(HAPC)患者血清甲状腺激素的变化及其临床意义。
Objective To investigate the alteration of serum thyroid hormone level in the patients with high altitude polycythemia (HAPC) and its clinical significance.
目的研究伴发于真性红细胞增多症的红斑性肢痛症发病机制、临床表现、病理生理特点。
Objective To study the mechanism, clinical manifestations and pathophysiological characteristics of erythromelalgia accompanying polycythemia vera.
目的探讨腹腔镜巨脾切除术在小儿遗传性球形红细胞增多症治疗中的可行性及效果评价。
Objective to explore the feasibility and the efficacy of laparoscopic splenectomy of massive splenomegaly in the treatment of hereditary spherocytosis in children.
目的了解真性红细胞增多症(PV)患者内源性红系集落(EEC)生长情况及其临床意义。
Objective To investigate the growth of endogenous erythroid colony (EEC) in polycythemia vera (PV) patients and its clinical significance.
结果①青紫组合并红细胞增多症者心肌酶学改变较非红细胞增多者明显升高（P＜005）；
Results The changes of myocardial enzyme in cyanosis group with polycythemia were significantly higher than those in the group without polycythemia( P< 0 05);
目的了解真性红细胞增多症患者的血液流变学特性变化，研究其并发症的发病机理和寻找预防和治疗的方法。
Objective To understand the changes ofhemorheological factors in these patients with in Polycythemia Vera and study its pathology in order to find the preventive and treating methods.
遗传性球形红细胞增多症中，窦状隙被RBC塞满，球形红细胞的渗透性脆性增加，因为RBC每单位体积的表面积减少。
The sinusoids are packed with RBC's in this case of hereditary spherocytosis. The osmotic fragility of spherocytes is increased, because the RBC's have decreased surface area per unit volume.
结论：高原红细胞增多症患者存在纤溶抑制功能的亢进及凝血与纤溶系统的紊乱，溶栓胶囊对高原红细胞增多症具有明显的防治效果。
Conclusion: the study indicated that it was related to disturbance or fibrinolysis coagulation system in the patients with HAPC and plasmin capsules were valuable in prevention and treatment of HAPC.
结论：高原红细胞增多症患者存在纤溶抑制功能的亢进及凝血与纤溶系统的紊乱，溶栓胶囊对高原红细胞增多症具有明显的防治效果。
Conclusion: the study indicated that it was related to disturbance or fibrinolysis coagulation system in the patients with HAPC and plasmin capsules were valuable in prevention and treatment of HAPC.
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