方法需行脾切除术的患者2 0例，包括肝硬化继发性脾亢4例，脾假性囊肿1例，遗传性球形细胞增多症1例，原发性血小板减少性紫癜14例。
Methods 20 cases underwent splenectomy, including 4 cases of hypersplenism secondary to hepatic cirrhosis, 1 case of pseudocyst of spleen, 14 cases of primary thrombocytopenic purpura.
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.
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.
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.
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).
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.
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.
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