A Case of Acute Hemolytic Anemia Induced by Intravenous High-Dose Immunoglobulin during the Treatment of Chronic Idiopathic Thrombocytopenic Purpura.
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概要
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A 4-year-old girl with chronic idiopathic thrombocytopenic purpura showed an acute hemolytic anemia after receiving intravenous high-dose immunoglobulin. The abnormalities were attributed to and-A antibody derived from the immunoglobulin products. The anemia accompanied with low haptoglobin (<10 mg/dl) returned to the normal level without blood transfusion within two weeks after the cessation of intravenous immunoglobulin therapy.
- 特定非営利活動法人 日本小児血液・がん学会の論文
特定非営利活動法人 日本小児血液・がん学会 | 論文
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