曾帆 1 , 劉云 1 , 周鵬 2 , 謝雪 1 , 常紅 1
  • 四川大學華西醫院(成都, 610041) 1 血液內科, 2 耳鼻喉/頭頸外科;
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【摘要】 目的  探討t(8;21)急性髓系白血病(acute myeloid leukemia,AML)的臨床特點及預后,提高對t(8;21)AML的認識。 方法  2010年5月收治1例t(8;21)AML患者,對其臨床資料并復習相關文獻進行分析。患者因乏力、皮下瘀斑入院,查體發現患者有胸骨壓痛,脾肋下3 cm觸及,血常規:白細胞80.37×109/L,異常細胞 23%,取患者骨髓液行形態學、流式細胞術檢測及染色體核型檢測。 結果  患者診斷為急性粒細胞白血病部分分化型(AML-M2b),AML1/ETO融合基因陽性,染色體核型分析t(8;21)(q22;q22)。 結論  t(8;21)AML是一類較為特殊的急性髓系白血病,在診斷時需尋找疾病的預后因素并進行分層,實施個體化治療。
【Abstract】 Objective  To obsrve the clinical features and prognosis of acute myeloid leukemia (AML) with t(8;21). Methods  The clinical data of one patient with t (8; 21) AML diagnosed in May 2010 was retrospectively analyzed. The chief complaints of the patient were malaise and ecchymosis. The physical examinations revealed sternum pain and splenomegaly; blood routine examination showed that the peripheral WBC count was 80.37×109/L, and the abnormal cells were 23%. Bone marrow samples were collected to perform the morphologic test, flow cytometry analysis and chromosome analysis. Results  The patient was diagnosed as AML with maturation (AML-M2) with positive AML1/ETO fusion gene and translocation (8; 21) (q22; q22). Conclusion  AML with t (8; 21) is different with other types of AML; patients with AML with t (8; 21) need individualized treatment.

引用本文: 曾帆,劉云,周鵬,謝雪,常紅. 急性髓系白血病伴t(8;21)的臨床特點及預后. 華西醫學, 2010, 25(11): 2004-2006. doi: 復制