Recurrent Chromosomal Abnormalities in Lymphomas in Fine Needle Aspirates of Lymph NodeReportar como inadecuado

Recurrent Chromosomal Abnormalities in Lymphomas in Fine Needle Aspirates of Lymph Node - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Collegium antropologicum, Vol.34 No.2 June 2010. -

The detection of specific chromosomal abnormalities is important in the diagnostic workup of aggressive lymphomas, giving its impact on the treatment strategies and prognosis. This has been accomplished by using the fluorescent in situ hybridisation method FISH performed on fine needle aspiration FNA specimens what is attractive in the diagnosis of lymphoma in the comparation with other methods for collecting samples. The cytogenetic analyses were performed in series of 80 patients with lymphoma 43 women and 37 men, median age 48, range 3–90 years. In our series 89.0% 71 of the specimens yield sufficient numbers of analysable metaphases, comprising 63 non-Hodgkin lymphomas NHL and 8 examples of Hodgkin disease HD. Among 71 successful karyotyped specimens 58 82.0% showed clonal karyotypic abnormalities. Numerical changes in 4, structural changes in 20 and both and numerical with structural changes in 30 of 54 NHL cases. Trisomies 3, 7, 8, 12, 18, X and monosomies 1 were most common numerical abnormalities. The NHL cases were typically characterised by structural rather than numerical aberrations with chromosome arms 1p-q, 3p-q, 6q, 11q, 17p and 14q most frequently involved. The expected translocation 14;18q32;q21 in 8 and t8;14q24;q34 in 6 cases, both translocations at the same time in three cases, complex rearrangement with chromosome 8, 14, and 18, namely t8;14;18q24;q32;q21 in one case, t11;14q13;q32 in three and one case with translocation 14q32 with chromosome 3q27, 6q and 14q32 were found. In 28 of 54 52% NHL cases t14;v was present. Four abnormal clones detected in Hodgkin disease were typically consisted of a small percentage of metaphases. The use of FISH method enable the detection of loss or gain of genetic material and reveal rearrangements unsuspected by conventional cytogenetics in 34 48.0% cases.

fine needle aspirate; lymphoma; cytogenetics

Autor: Ružica Lasan Trčić - Dunja Šusterčić - Maja Kuspilić - Biljana Jelić-Pupškarić - Iris Fabijanić - Ika Kardum-Skelin -



Documentos relacionados