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.
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