Hello
CLL fellows and Specialists, Hematologists
I want to share my experience here. We have been fortunate to meet Dr. Christen Chen at the Princes Margaret Cancer Hospital in Toronto. She is very kind and friendly. She has ordered several tests one of them is a FISH test and it is reported as trisomy 12,13q deletion. I want to hear about the results of my wife. I really want to know the following interpretation:
"The signal pattern observed for the chromosome 12 centromere probe showed trisomy 12 in 66.5% of nuclei.
Trisomy 12 is recurrently seen in
multiple lymphoid neoplasms including CLL, mantle cell lymphoma, and follicular lymphoma. In the setting of CLL it is associated with an intermediate prognosis.
The signal pattern observed for the D13S319/D13S25 probe showed a 13q deletion in 50% of nuclei.
The signal patterns observed for the remaining 2 probes (ATM and TP53) were within normal limits
"
I look forward to having comments on it!
Sagar