ππ»π°πΌπ»π°πΉπππΆππ² π³πΆπ»π±πΆπ»π΄π
The bone marrow biopsy results indicate an expanded erythropoiesis and relatively reduced myelopoiesis. There are no clear abnormalities in megakaryopoiesis or an increase in myeloblasts, and the marrow is not notably cell-rich. Therefore, there are no definite indications of myeloproliferative neoplasia (MPN). The changes are primarily interpreted as reactive/secondary.
However, this interpretation was made with incorrect information stating that jak2 was negative; it is uncertain, meaning they have found a jak2 mutation. Combined with persistent HB above 18, hematocrit up to 54%, and EPO below normal values, it sounds to me like PV. What are your thoughts? It has also been investigated for secondary polycythemia with no findings. Age 37.
Dont get me wrong, the best would, of course, be that there was nothing. But when symptoms like red skin, high blood pressure, fatigue, tingling legs, gout, and blurred vision are present. In addition to most people with the JAK2 mutation having MPN, and both HB, Hematocrit, and EPO indicate MPN, I can't settle for that.
Anyone had results like this?