I have a question regarding my father's FISH results. They read:
An abnormal FISH signal pattern of 2R3G was observed in t(4;14) probe set. This finding is consistent with an IGH gene rearrangement to an unidentified gene that is not FGFR3.
An abnormal FISH signal pattern of 2R3G was observed in t(14;16). This finding is consistent with an IGH rearrangment to an unidentified gene that is not MAF.
Duplication of 1q in 72.3% of nuclei.
The 11;14 probe set showed an abnormal signal pattern (2R3G) displaying an extra copy of the IGH locus suggestive of trisomy/hyperdiploidy of chromosome 14 or IGH gene rearrangement with an unidentified chromosomal partner. This is an abnormal result but NEGATIVE for CCND1/IGH fusion.
Does this mean there is a translocation 4,14 and also a translocation 14,16 -- i.e., t(4;14) and t(14;16)?
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Helen521 - Who do you know with myeloma?: father (Smoldering)
- When were you/they diagnosed?: Sept 2016
- Age at diagnosis: 65
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