Primary thrombocythemia is the overproduction of platelets without a known cause. Platelets are essential for blood clotting.
Essential thrombocythemia; Essential thrombocytosis
Primary thrombocythemia is a disorder that slowly progresses. It is caused by too much growth of a type of cell that is used to make blood cells. Although the platelets are mostly affected, the red blood cells and white blood cells may also be involved.
The disease is in the same family of disorders as:
Usually it affects people in middle age. It can also be seen in younger patients, especially females under age 40.
People with this condition make too many platelets and may have a problem with blood clots (thrombosis). Because these platelets do not work well, bleeding is also a common problem.
- Bleeding from the gastrointestinal tract, respiratory system, urinary tract, or skin
- Bleeding from the gums
- Easy bruising
Enlarged lymph nodes (rare)
- Nosebleeds (epistaxis)
- Numbness of the hands or feet
- Prolonged bleeding from surgical procedures or tooth extraction
- Ulcers on the fingers or toes
The condition may even cause strokes in some people.
This condition is often detected on blood tests done for other reasons, before there are any symptoms.
A physical exam may show an enlarged spleen or liver.
Other tests may include:
The outcome varies. Most people go long periods of time without complications and have a normal life expectancy. In a very small minority of patients, complications from hemorrhage and thrombosis lead to death.
Call your health care provider:
If a patient has life-threatening complications, a procedure to remove platelets directly from the blood (platelet pheresis) can rapidly decrease the platelet count.
Long-term use of medications to decrease the platelet count can reduce both bleeding and clotting complications. The most commonly used medications include hydroxyurea, interferon-alpha, or anagrelide. In patients who have a tendency to clot, aspirin may help decrease clotting episodes.
Many patients do not need any treatment. However, the health care provider should monitor their condition.
Tefferi A. Myeloproliferative disorders: Essential thrombocythemia and primary myelofibrosis. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier;2007:chap 177.
Review Date: 3/2/2009
Reviewed By: David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; and Yi-Bin Chen, MD, Leukemia/Bone Marrow Transplant Program, Massachusetts General Hospital. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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