l

FISH showing Trisomy 12 in chronic lymphocytic leukemia (CLL)

FISH showing Trisomy 12 in chronic lymphocytic leukemia (CLL)
#00061454
Author: Mr Anil Kumar Yadav, Dr Manorama Bhargava, India
Category: Lymphoma: Mature B-cell and Plasma cell Neoplasms > Low-grade B-cell lymphoma > Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Published Date: 05/29/2018

A 67-year-old man with chronic lymphocytic leukemia (CLL) having 61% lymphocyte on peripheral blood (PB). Fluorescence in situ hybridization (FISH) detected trisomy 12 in 15% of the cells analysed [30/200]. Trisomy 12 is found in 15-20%[cytogenetics-karyotyping] or 16-25 %[FISH] of CLL cases  [http://atlasgeneticsoncology.org/Anomalies/CLLID2034.html]. FISH analysis for TP53 gene deletion (DC-Dual colour) and IgH breakapart (DC, BA) shows negative for deletion and gene rearrangement respectively in all the cells analysed (100%).  

FISH with the CEN 12 Probe (Zytovision) on a peripheral blood cell sample, showing three interphase nuclei with two orange signal (in two cells- top and bottom nucei) and three orange signals (nuclei with trisomy 12- in centre).