It sounds like confirmation of what you already know. In the absence of an identified cause of reactive thrombocytosis, you will need to wait on the genetic tests to make the next set of decisions. If you are positive for a driver mutation, the answer would be more clear. If you are negative for driver mutations, then you are going to have to decide whether a BMB is warranted. I do not think there is a clear choice here. It may be more about your preference in how to handle the assessment process.
You would have to check the reference range being used by your lab to answer that question. The reference range varies by lab.
The 2016 WHO diagnostic criteria for PV include these criteria.
Hemoglobin > 16.5 g/dL in men and > 16 g/dL in women, or hematocrit > 49% in men and > 48% in women, or red cell mass > 25% above mean normal predicted value.
Your HGB and HCT fall below these levels. You would not meet criteria to consider a diagnosis of PV based on these numbers.
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