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RBM15‐MKL1 (OTT‐MAL) fusion transcript in an adult acute myeloid leukemia patient
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...
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Published in: | American journal of hematology 2005-05, Vol.79 (1), p.43-45 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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). Am. J. Hematol. 79:43–45, 2005. © 2005 Wiley‐Liss, Inc. |
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ISSN: | 0361-8609 1096-8652 |
DOI: | 10.1002/ajh.20298 |