A UNIQUE CASE OF T(15 17) ACUTE PROMYELOCYTIC LEUKEMIA (M3) DEVELOPING INTO ACUTE MYELOBLASTIC-LEUKEMIA (M1) WITH T(7 21) AT RELAPSE

被引:31
作者
JUBASHI, T
NAGAI, K
MIYAZAKI, Y
NAKAMURA, H
MATSUO, T
KURIYAMA, K
TOMONAGA, M
机构
[1] Department of Haematology, Atomic Disease Institute, Nagasaki University School of Medicine
关键词
D O I
10.1111/j.1365-2141.1993.tb04709.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This report describes a case of t(15;1 7) acute promyelcytic leukaemia (APL, FAB subtype M3) with dysgranulopoiesis at diagnosis in a patient who developed myelodysplasia (MDS) and then a second phenotype of t(7;21) acute myeloblastic leukaemia (AML, FAB subtype M 1) at the time of relapse. To our knowledge, there is no report of a second phenotype of AML occurring after complete remission (CR) of APL. Furthermore, this is the first report of chromosomal abnormality t(7;2 1) in a case of AML. Several hypotheses for this unusual course of APL are discussed.
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页码:665 / 668
页数:4
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