Title of article :
Clonal evolution of an immunoblastic type non-Hodgkinʹs lymphoma with der(6)t(1;6)(q11;p11) as its primary cytogenetic abnormality
Author/Authors :
Gagos، Mariusz نويسنده , , Sarantis and Iatridou-Kyrkou، نويسنده , , Kalliopi and Liosi، نويسنده , , Anna and Karakitsos، نويسنده , , Petros and Papageorgaki، نويسنده , , Pagona and Kyroudi، نويسنده , , Aspassia and Pathak، نويسنده , , Sen، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1995
Abstract :
Recurrent pleural effusions from a 45-year-old man who was diagnosed as having non-Hodgkinʹs lymphoma of immunoblastic type were studied cytogenetically. The majority of the metaphases were tetraploid, but there were also lymphoma cells observed with pseudodiploid chromosome constitutions. Cytogenetic analysis by G-banding revealed the existence of at least two cell populations. The karyotype of the minor pseudodiploid clone, which exhibited partial trisomy of 1q11qter and monosomy of 6p11pter as sole abnormalities, was 46,XY,der(6)t(1;6)(q11;p11). The karyotype of the major clone was 92,XXYY, −1,der(6)t(1;6)(q11;p11)x2, +9. The ancestral diploid clone, carrier of the balanced translocation involving chromosomes 1 and 6, was not observed even in the first pleural effusion harvest. The high proportion of tetraploid cells in the recurrent effusions was an indication that these cells were favorably selected in the environment of the somatic cavity. Our cytogenetic findings suggest that partial trisomy of 1q may be a crucial secondary chromosomal abnormality in highly malignant non-Hodgkinʹs lymphoma. This genetic imbalance was predetermined from the primary abnormality and may be responsible for further tumor progression, as suggested from the clonal evolution in this particular case and, therefore, may be associated with the aggressive biologic behavior of malignant cells.
Journal title :
Cancer Genetics and Cytogenetics
Journal title :
Cancer Genetics and Cytogenetics