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

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;p15), which...

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Bibliographic Details
Published in:Cancer genetics and cytogenetics 1996, Vol.86 (1), p.72-75
Main Authors: Inaba, Tohru, Shimazaki, Chihiro, Yoneyama, Satoshi, Hirai, Hideyo, Kikuta, Takehisa, Sumikuma, Toshiya, Sudo, Yoshikazu, Yamagata, Noboru, Ashihara, Eishi, Goto, Hideo, Fujita, Naohisa, Nakagawa, Masao
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Language:English
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Summary: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;p15), 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.
ISSN:0165-4608
1873-4456
DOI:10.1016/0165-4608(95)00160-3