Complex translocation involving chromosomes #1, #9, and #22 in a patient with chronic myelogenous leukemia

A case of Philadelphia chromosome positive chronic myelogenous leukemia with a complex translocation involving chromosomes #1, #9, and #22 is described. All cells in the bone marrow showed this rearrangement, and Q-banding analysis showed the predominant karyotype to be 46,XY, t(1;9;22)(p22;q34;q11).     

A novel translocation involving chromosomes 2, 9, 14, and 22 in chronic myeloid leukemia

A 46-year-old man with chronic myelogenous leukemia was found to have a new complex translocation. In chronic phase, all of the bone marrow cells had a rearrangement of a t(2;9;14;22) (p21;q34;q32;q11). Southern blot analysis of leukocyte DNA revealed rearrangement of the breakpoint cluster region (bcr) within the 5.8-Kb bcr. The patient eventually died in blast crisis 28 months later. The cytogenetic findings of bone marrow cells showed a 46,XY,t(2;9;14;22)(p21;q34;q32;qll),add(lp),del(3q) karyotype in blast crisis.     

Unusual translocations involving chromosomes 12;22 and 9;12 in a case of chronic myelogenous leukemia

A case of chronic myelogenous leukemia (CML) with highly unusual translocations involving both chromosomes #12 is reported. The origin of the Ph1 chromosome was due to a 12p/22q translocation. Chromosome #9 was involved in a translocation with the other chromosome #12. By critical examination of the "size" of the Philadelphia chromosome, it was noted that the breakpoints on 22q were different when compared with a previous case (see Verma and Dosik [16]), although the short arm of chromosome #12 (12p) was involved in both instances. So far, no apparent differences in the course of the disease have been attributed to the types of translocation observed in these cases.     

Ph-negative chronic myelocytic leukemia with a complex translocation involving chromosomes 7 and 11

A complex translocation t(7;11)(7qter----7p15::11q13----11qter;11pter ----11p15::11q13----11p15::7p15----7pter) was detected in the leukemic cells from a 67-year-old woman with Ph chromosome negative chronic myelocytic leukemia. This translocation has not been previously reported in Ph-negative CML.     

Complex translocation involving Ph chromosome in a patient with typical chronic myelogenous leukemia.

We report a cytogenetic study of a patient with chronic myelogenous leukemia (CML) who, while displaying a Philadelphia (Ph) chromosome, resulting from a standard t(9;22) at diagnosis, during the chronic phase (CP) showed disappearance of the Ph and occurrence of new chromosome changes, including a marker probably arising from a translocation involving chromosome 17 and the Ph. In situ hybridization confirmed the cytogenetic appearance and demonstrated that the breakpoint on the Ph marker occurred below the BCR-ABL fusion gene.     

Myxoid chondrosarcoma with a translocation involving chromosomes 9 and 22

Myxoid chondrosarcoma is an uncommon neoplasm thought to be derived from mesenchymal chondrocytic cells. Although cytogenetic abnormalities have been reported in sarcomas, too few cases have been studied to determine the frequency of nonrandom chromosomal changes in mesenchymal tumors. In this article, we describe a chondrosarcoma with a nonrandom reciprocal translocation t(9;22)(q22;q11). The cellular homologue to the retrovirus transforming gene of simian sarcoma virus is located on chromosome #22, and its possible significance in this case is discussed.     

Reciprocal translocation between chromosomes 8 and 9 in atypical chronic myeloid leukaemia.

A balanced translocation t(8;9) (p11;q34) was present in the peripheral blood, bone marrow, and spleen cells of a patient with Ph negative chronic myeloid leukaemia. Subsequent transformation into acute leukaemia was associated with the emergence of trisomy 8 and der(8)(8qter----cen----8p11::9q34----9qter). This is the third reported case of t(8;9) (p11;q34) and raises the question of the role of c-abl in the pathogenesis of this myeloproliferative disorder.     

Masked Ph chromosome due to a new type of translocation in a patient with chronic myelogenous leukemia

A chronic myelogenous leukemia patient with a masked Ph chromosome due to a new type of translocation, t(9;11;22)(q34;p11;q11), is reported.     

Philadelphia-positive thrombocythemia with a complex translocation involving chromosomes 9, 15, and 22

We report a case of Philadelphia chromosome (Ph) positive thrombocythemia with a complex translocation. G-banding analysis showed the predominant karyotype to be 46,XX,t(9;15;22). Southern blot analysis revealed a rearrangement within the breakpoint cluster region on chromosome 22 similar to findings in chronic myeloid leukemia. These data suggest the presence of a complex Ph translocation involving t(9;15;22)(q34.1 or q34.3;q26.1;q11 or q13).     

Juvenile chronic myelogenous leukemia with abnormalities of chromosomes 4 and 5

A case of a boy with juvenile chronic myelogenous leukemia (CML) and independent clonal abnormalities of chromosomes 4 and 5 is presented. The characteristics and cytogenetics of CML are discussed, as is the involvement of chromosomes 4 and 5 in hematologic malignancies. The significance of these karyotypic findings in juvenile CML is explored.     

Chronic myelogenous leukemia with a complex translocation

A case of Philadelphia chromosome (Ph¹)-positive chronic myelogenous leukemia (CML) with a complex translocation involving chromosomes #3, #9, and #22 is described. All cells in the bone marrow showed this rearrangement and Q-banding analysis showed the karyotype to be 46, XX, t(3;9;22) (p21;q34;q11). This is the third reported case of a 3/9/22 rearrangement in the Ph¹-positive CML in which the break points and direction of transposition of chromosome segments are identical.     

Chronic myelogenous leukemia (CML) with translocation (8;22): a new variant

A case of chronic myelogenous leukemia (CML) in a young woman with a new variant Ph1-translocation--i.e., t(8;22) (q24;q12)--is described. The clinical and biological aspects of the disease did not seem to differ from those of the usual cases of CML.