Molecular implications of Ph (+) myelodysplastic syndrome.

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Abstract

We report a case of 62-year-old Japanese male with a myelodysplastic syndrome (MDS) with a Philadelphia (Ph) chromosome. Cytogenetic analysis revealed the bone marrow cells to contain a Ph chromosome due to t(?;11;22) (?;q11;q11), as well as -5, -7, +8, -12 and an extra Ph, in addition to cells with a normal karyotype. Molecular analysis using breakpoint cluster region probes (5' bcr and 3' bcr) did not detect a rearrangement within the bcr DNA sequences, indicating that the breakpoint at 22q11 occurred outside the bcr. Furthermore, the bone marrow cells from this patient did not express an 8.5 kb c-abl mRNA. Thus, the Ph translocation in this case differs from that of Ph-positive chronic myelogenous leukemia.

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Toyama, K., Ohyashiki, K., & Ohyashiki, J. H. (1988). Molecular implications of Ph (+) myelodysplastic syndrome. Advances in Experimental Medicine and Biology, 241, 67–71. https://doi.org/10.1007/978-1-4684-5571-7_10

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