My husband has just been diagnosed with CLL. We got the results from the FISH test and he has mostly good prognostic indicators: CD38-, Zap-70-, and mutated lgVH. The folowing deletions were identified:
13q14.3 loss of 935.70kb
14q32.33 loss of 660.68kb
Does anyone know how to interpret the "loss of" numbers? (Can that be translated into what % of the chromosone is missing?) Also, I have not found much information about the 14q.32.22 deletion and it's relationship when it's combined with a 13q14.3 deletion.
Thanks for your input!
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kreale
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This is the first discussion I have seen with regard to an additional chromosomal abnormality with a !3q-. I have 13.q- (Dleu1) and a 14q.32+ (assumed translocation, but not with 11q14 which I understand would be bad).
I Understand that FISH testing only tests for the probes provided and whatever partner this 14q+ has might not be anything probed for. In any case, FISH testing is not all that useful in watch and wait and prognosis is not a prediction.
However, having said that, I have had an ongoing curiosity about what this second error might indicate. It has resulted in my prognosis being "neutral" and not the "positive" that a solo 13q- would generate.
I have looked for any information on prognosis with a second chromosome error plus the 13q-. The ranking of prognosis always only has 13q- solo or ranks "more than one error". I also can't find much on the 14q32+ and what that might mean. in terms of numbers, I have many times more of the 14q+ than the 13q-. Just wondering. I am a curious person
Cilcanada -Thank you for your response. Do you know how to translate the deletion loss in kb to percentage of loss? For example, my husband has a deletion of 13q14.3 loss of 935.70.
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