Polycythaemia Vera (PV)

Polycythaemia Vera (PV): Symptoms, Causes, Diagnosis, Treatment, and Future Outlook.

Disclaimer:
This blog is for informational purposes only and should not be taken as medical advice. Content is sourced from third parties, and we do not guarantee accuracy or accept any liability for its use. Always consult a qualified healthcare professional for medical guidance.

What is Polycythaemia Vera (PV)?

Polycythaemia Vera (PV) is a chronic myeloproliferative neoplasm where the bone marrow overproduces red blood cells, often white cells and platelets, leading to blood thickening and complications. It’s driven by JAK2 mutation (95% of cases), classified as a slow-progressing cancer. In 2025, ~3,000 US cases annually, median age 60, more in men.

Symptoms

Symptoms include fatigue, headaches, dizziness, visual disturbances, itching (after hot baths), redness (ruddy complexion), burning pain in hands/feet (erythromelalgia), gout, abdominal fullness (splenomegaly), and bleeding/bruising. Many are asymptomatic. Complications include blood clots (stroke, heart attack) or transformation to myelofibrosis/AML (10-20%).

Causes

The primary cause is JAK2 V617F mutation (95%), with rare TET2/CALR mutations. Risk factors include age (over 60), male gender, and family history (rare). No strong environmental links, but radiation or benzene exposure suspected. In 2025, clonal hematopoiesis is a precursor.

Diagnosis

Diagnosis uses CBC showing high hemoglobin/hematocrit/red cells, bone marrow biopsy for hypercellularity, JAK2 testing, and EPO levels (low). Ultrasound assesses spleen. In 2025, NGS detects additional mutations for risk.

Treatment

Treatment reduces blood viscosity: phlebotomy (hematocrit <45%), low-dose aspirin for clotting prevention, and cytoreductive therapy (hydroxyurea, ruxolitinib for high-risk). Interferon-alpha for young patients. In 2025, ruxolitinib improves symptom control.

Future Outlook

In 2025, median survival is 20 years with treatment, but 20% progress to fibrosis/AML. JAK2 inhibitors extend disease-free survival. By 2030, gene therapies could cure PV.

Sources

The information is based on Mayo Clinic’s “Polycythemia vera – Symptoms & causes” for symptoms; Cleveland Clinic’s “Polycythemia Vera: What It Is, Symptoms & Treatment” for overview; NCBI’s “Polycythemia Vera – StatPearls” for diagnosis; WebMD’s “Polycythemia Vera (PV): Symptoms, Causes, Diagnosis” for causes; Healthline’s “Polycythemia Vera Outlook and Life Expectancy” for outlook; YouTube’s “Understanding polycythemia vera (PV): Diagnosis, treatments” for treatment; Pharmacy Times’s “The Evolving Landscape of Polycythemia Vera Treatment” for updates; The Oncology Nurse’s “Getting Closer to Disease Modification in Polycythemia Vera” for future; Johns Hopkins’s “Polycythemia Vera” for symptoms; Texas Oncology’s “Polycythemia Vera” for overview.