Polycythemia vera: 2024 update on diagnosis, risk‐stratification, and management
Mayo Clinic · Ospedale Papa Giovanni XXIII
Abstract
DISEASE OVERVIEW: Polycythemia vera (PV) is a JAK2-mutated myeloproliferative neoplasm characterized by clonal erythrocytosis; other features include leukocytosis, thrombocytosis, splenomegaly, pruritus, constitutional symptoms, microcirculatory disturbances, and increased risk of thrombosis and progression into myelofibrosis (post-PV MF) or acute myeloid leukemia (AML). DIAGNOSIS: A working diagnosis is considered in the presence of a JAK2 mutation associated with hemoglobin/hematocrit levels of >16.5 g/dL/49% in men or 16 g/dL/48% in women; morphologic confirmation by bone marrow examination is advised but not mandated. CYTOGENETICS: Abnormal karyotype is seen in 15%-20% of patients with the most frequent…
Citation impact
- FWCI
- 47.89
- Percentile
- 100%
- References
- 207
Authors
2Topics & keywords
- Medicine
- Leukocytosis
- Internal medicine
- Polycythemia vera
- Thrombocytosis
- Myelofibrosis
- Myeloproliferative neoplasm
- Gastroenterology
- Good health and well-being