Mj. Macera et al., NEW TRANSLOCATIONS [T(6,15)(P25,Q22) AND T(6,19)(Q16,Q13.3)] WITH T(9,22)(Q34,Q11) IN A PH-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA, Cancer genetics and cytogenetics, 72(1), 1994, pp. 65-67
A case with typical features of chronic myelogenous leukemia (CML) wit
h two complex-aberrations in addition to the standard t(9;22) is repor
ted. Cytogenetic evaluation of the patient's bone marrow cells (BMC) s
howed 46,XX,t(6;19) (q16;p13.3),t(9;22)(q34;q11) in 60% of the mitotic
cells and 46,XX,idem, t(6;15)(p25;q22) in the remaining 40% dividing
cells. The patient's peripheral blood smear exhibited the usual differ
ential observed in chronic-phase CML and was clinically indistinguisha
ble from patients with the t(9;22) as the only translocation. We perfo
rmed Southern blotting on BgllI-digested DNA with the Trans-Probe (OSI
) and in addition to the 4.8-, 2.3-, and 1.1-kilobase (kb) germline fr
agments, we detected on additional fragment at 7 kb. This probe spans
the entire 5.8-kb M-breakpoint cluster region (BCR), and a single brea
kpoint in this region will appear as either one or two additional frag
ments. Because only one additional fragment was observed, both cell li
nes apparently share the same breakpoint in the ABL/BCR gene. Apparent
ly the second aberrant cell line with the additional t(6;15) represent
s clonal evolution of the original abnormal clone.