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Essential thrombocythemia

Blood cellsBlood cells

Primary thrombocythemia; Essential thrombocytosis

Definition

Essential thrombocythemia (ET) is a condition in which the bone marrow produces too many platelets. Platelets are particles in the blood that aid in blood clotting.

Causes

ET results from an overproduction of platelets. As these platelets do not work normally, blood clots and bleeding are common problems. Untreated, ET worsens over time.

ET is part of a group of conditions known as myeloproliferative disorders. Others include:

Chronic myelogenous leukemia (an overproduction of white blood cells that starts in the bone marrow)
Polycythemia vera (bone marrow disease that leads to an abnormal increase in the number of red blood cells)
Primary myelofibrosis (disorder of the bone marrow in which the marrow is replaced by fibrous scar tissue)

Many people with ET have a mutation of a gene (JAK2, CALR, or MPL).

ET is most common in middle-aged people. It can also sometimes be seen in younger people, especially women under age 40.

Symptoms

Symptoms may include any of the following:

Headache (most common)
Tingling, coldness, or blueness in the hands and feet
Feeling dizzy or lightheaded
Vision problems
Mini-strokes (transient ischemic attacks) or stroke

If bleeding is a problem, symptoms may include any of the following:

Easy bruising and nosebleeds
Bleeding from the gastrointestinal tract, respiratory system, urinary tract, or skin
Bleeding from the gums
Prolonged bleeding from surgical procedures or tooth removal

Exams and Tests

Most of the time, ET is found through blood tests done for other health problems before symptoms appear.

Other tests may include:

Bone marrow biopsy
Complete blood count (CBC)
Genetic tests (to look for a change in the JAK2, CALR, or MPL gene)

Treatment

If you have life-threatening complications, you may have a treatment called platelet pheresis. It quickly reduces the number of platelets in the blood.

Long-term, medicines are used to decrease the platelet count to avoid complications. The most common medicines used include hydroxyurea, interferon-alpha, or anagrelide.

Aspirin at a low dose (81 to 100 mg per day) may decrease clotting episodes.

Many people do not need any treatment, but they must be followed closely by their provider.

Outlook (Prognosis)

Outcomes may vary. Most people can go for long periods without complications and have a normal lifespan. In a small number of people, complications from bleeding and blood clots can cause serious problems.

In rare cases, the disease can change into acute leukemia or myelofibrosis.

Possible Complications

Complications may include:

Acute leukemia or myelofibrosis
Severe bleeding (hemorrhage)
Stroke, heart attack, or blood clots

When to Contact a Medical Professional

Contact your provider if:

You have unexplained bleeding that continues longer than it should.
You notice chest pain, leg pain, confusion, weakness, numbness, or other new symptoms.

References

Gotlib J. Polycythemia vera, essential thrombocythemia, and primary myelofibrosis. In: Goldman L, Schafer AI, eds. Goldman-Cecil Medicine. 26th ed. Philadelphia, PA: Elsevier; 2020:chap 157.

Marcellino BK, Mascarenhas J, Iancu-Rubin C, Kremyanskaya M, Najfeld V, Hoffman R. Essential thrombocythemia. In: Hoffman R, Benz EJ, Silberstein LE, et al, eds. Hematology: Basic Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 71.

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Review Date: 2/2/2023

Reviewed By: Mark Levin, MD, Hematologist and Oncologist, Monsey, NY. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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