t(7;11) and Trilineage myelodysplasia in acute myelomonocytic leukemia

被引:8
作者
Inaba, T
Shimazaki, C
Yoneyama, S
Hirai, H
Kikuta, T
Sumikuma, T
Sudo, Y
Yamagata, N
Ashihara, E
Goto, H
Fujita, N
Nakagawa, M
机构
[1] Second Department of Medicine, Kyoto Pref. University of Medicine, Kyoto
[2] Second Department of Medicine, Kyoto Pref. University of Medicine, 602 Kyoto, Kawaramachi-hirokoji, Kamigyo-ku
关键词
D O I
10.1016/0165-4608(95)00160-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A 48-year-old Japanese man was admitted to our hospital because of general fatigue, nasal bleeding, and petechiae on his extremities. He was diagnosed with acute myelomonocytic leukemia with trilineage myelodysplasia (T-MDS). Chromosomal analysis of bone marrow cells revealed t(7;11)(p15;p25), which has been rarely reported but known to be characteristic of Japanese patients. Although t(7;11)(p15;p15) has been reported mainly in acute myelogenous leukemia (AML), it can be occasionally found in so-called stem cell diseases such as chronic myelogenous leukemia or chronic myeloproliferative disorders. Therefore, t(7;11)(p15;p15) might affect trilineage progenitors or stem cells as well as myeloid lineage cells, subsequently resulting in AML with T-MDS, as in our case reported here.
引用
收藏
页码:72 / 75
页数:4
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