摘要
The t(1;22)(p13;q13) is a nonrandom chromosomal abnormality in acute leukemia with the fusion oncogene, RBM15-MKL1 (OTT-MAL), identified recently. However, this abnormality has been described only in infants and young children with acute megakaryoblastic leukemia (AMKL). We report a 59-year-old male patient with the diagnosis of acute myeloid leukemia, subtype M1, who harbors an abnormal chromosome +der(1)t(1;22)(p13;q13). The RBM15-MKL1 (OTT-MAL) fusion transcript was also confirmed by the reverse transcriptase-polymerase chain reaction. This unusual abnormality is rare in adult cases of leukemia, and in children it is restricted to AMKL. This report is accompanied by a review of the literature on the t(1;22)(p13;q13).
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 43-45 |
| 頁數 | 3 |
| 期刊 | American Journal of Hematology |
| 卷 | 79 |
| 發行號 | 1 |
| DOIs | |
| 出版狀態 | 已出版 - 05 2005 |
| 對外發佈 | 是 |
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