Progression from myelodysplastic syndrome to acute lymphoblastic leukaemia with Philadelphia chromosome and p190 BCR-ABL transcript

被引:24
作者
Kohno, T
Amenomori, T
Atogami, S
Sasagawa, I
Nakamura, H
Kuriyama, K
Tomonaga, M
机构
[1] Department of Haematology, Atomic Disease Institute, Nagasaki Univ. School of Medicine, Nagasaki
[2] Department of Haematology, Atomic Disease Institute, Nagasaki Univ. School of Medicine, Nagasaki 852
关键词
myelodysplastic syndrome; acute lymphoblastic leukaemia; common phenotype; Philadelphia chromosome; BCR-ABL;
D O I
10.1046/j.1365-2141.1996.4931034.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We describe a patient with Philadelphia chromosome (Ph(1))-positive acute lymphoblastic leukaemia (ALL) who developed it 2.5 years after being diagnosed with myelodysplastic syndrome (MDS). The patient initially had refractory anaemia (RA), but progressed to refractory anaemia with excess blasts (RAEB) 2 years later, that terminated in ALL, An immunophenotypic analysis of the lymphoblasts revealed CD10 and CD19 positive cells, The karyotype was normal 46,XY in RA phase, 46,XY,20q-during the RAEB phase, and 46,XY, t(9;22)(q34;q11), 20q-during the ALL phase. Furthermore, p190 BCR-ABL mRNA was detected in the ALL blasts, These findings indicate that this ALL arose from the MDS clone through multiple cytogenetic evolutions, the final event of which was the acquisition of p190 BCR-ABL type Ph(1).
引用
收藏
页码:389 / 391
页数:3
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