My hematologist said it was suspicious but he needed the biopsy to confirm the diagnosis. When he got a normal result back from the biopsy he said he called the head of the lab to find out how it could have come out with those results and was told that the gene test was probably a false positive but I just can't relax knowing it was "probably" a false positive. I don't take any medication other than vitamin d to account for the elevated WBC. I am going to have to ask him to rerun the gene test and see if it comes out positive again. Was hoping to see if anyone else has ever been through something similar and how it worked out for them. When I was first told of the positive gene test he said that CML was the best to hope for so getting worried that it is something that isn't as easily controlled with medication.
Hi, what you need to do is get a copy of that test which may talk about finding the Phila Chromosome. Maybe it's even online? If it does say that, then the next step would be to find out the odds of a false positive.
The word "suspicious" stands out in your account, being far from "conclusive".
On such an odd circumstance, I'd even wonder about a lab mixup or error.
A WBC of 18 is not necessarily a sign of a blood cancer. Other causes can get it that high, even taking corticosteroids.
AFAIK, a person can be Ph- and still have CML, Or be Ph+ and have some other leukemia. But your case doesn't makes sense. Maybe you can ask to be tested for the BCR protein that would be present if a person really has the Ph+. Or maybe tesed for tyrosine kinase. This is all just guesswork on my part.