Clonal evolution from trisomy into tetrasomy of chromosome 8 associated with the development of acute myeloid leukemia from myelodysplastic syndrome

Tetrasomy 8, though rare, is usually associated with trisomy 8, a far more common chromosomal abnormality in acute myeloid leukemia (AML). Yet the clonal relationship between trisomy 8 and tetrasomy 8 in the cases with these chromosomal abnormalities has been unclear. Here, we report a case of a 17-...

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Veröffentlicht in:Cancer genetics and cytogenetics 2001-01, Vol.124 (2), p.159-164
Hauptverfasser: Kameoka, Junichi, Funato, Tadao, Obara, Yasuhiko, Kadowaki, Ikuko, Yokoyama, Hisayuki, Kimura, Tomofumi, Tomiya, Yasuo, Yamada, Minami, Ishikawa, Izumi, Takagawa, Masanori, Sasaki, Osamu, Kimura, Jun, Harigae, Hideo, Miura, Ikuo, Meguro, Kuniaki, Kaku, Mitsuo, Sasaki, Takeshi
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Sprache:eng
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Zusammenfassung:Tetrasomy 8, though rare, is usually associated with trisomy 8, a far more common chromosomal abnormality in acute myeloid leukemia (AML). Yet the clonal relationship between trisomy 8 and tetrasomy 8 in the cases with these chromosomal abnormalities has been unclear. Here, we report a case of a 17-year-old male, diagnosed as having a myelodysplastic syndrome (MDS). Chromosome analysis showed the presence of trisomy 8. Five years later, he developed overt AML exhibiting tetrasomy 8 only. After chemotherapy, the blast cells in the bone marrow decreased to 3.4%, and the karyotype showed trisomy 8 alone. Fluorescence in situ hybridization using a probe specific for chromosome 8 showed that the percentages of cells exhibiting 2/ 3 /4 signals were 7.8/89.2/2.0 at the MDS stage, 20.5/36.1/41.0 when overt AML developed and 24.0/72.1/2.4 after chemotherapy. These results suggested that tetrasomy 8 is derived from the AML clone, possibly evolved from the MDS clone with trisomy 8. To our knowledge, this is the first detailed case report of clonal evolution from trisomy 8 into tetrasomy 8 associated with the development of AML from MDS.
ISSN:0165-4608
1873-4456
DOI:10.1016/S0165-4608(00)00347-2