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Thrombocytosis

Thrombocytosis is the presence of high platelet counts in the blood, and can be either reactive or primary (also termed essential and caused by a myeloproliferative disease). Although often symptomless (particularly when it is a secondary reaction), it can predispose to thrombosis in some patients. more...

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Generally, a normal platelet count ranges from 150,000 and 450,000 per mm3. These limits, however, are determined by the 2.5th lower and upper percentile, and a deviation does not necessary imply any form of disease. Nevertheless, counts over 750,000 (and especially over a million) are considered serious enough to warrant investigation and intervention.

Signs and symptoms

High platelet levels do not necessarily signal any clinical problems, and are picked up on a routine full blood count. However, it is important that a full medical history be elicited to ensure that the increased platelet count is not due to a secondary process. Often, it occurs in tandem with an inflammatory disease, as the principal stimulants of platelet production (e.g. thrombopoietin) are elevated in these clinical states as part of the acute phase reaction.

High platelet counts can occur in patients with polycythemia vera (high red blood cell counts), and is an additional risk factor for complications.

A very small segment of patients report symptoms of erythromelalgia, a burning sensation and redness of the extremities that resolves with cooling and/or aspirin use.

Diagnosis

Laboratory tests might include: full blood count, liver enzymes, renal function and erythrocyte sedimentation rate.

If the cause for the high platelet count remains unclear, bone marrow biopsy is often undertaken, to differentiate whether the high platelet count is reactive or essential.

Causes

Increase platelet counts can be due to a number of disease processes:

  • Essential (primary)
    • Essential thrombocytosis (a form of myeloproliferative disease)
    • Other myeloproliferative disorders such as chronic myelogenous leukemia, polycythemia vera, myelofibrosis
  • Reactive (secondary)
    • Inflammation
    • Surgery (which leads to an inflammatory state)
    • Hyposplenism (decreased breakdown due to decreased function of the spleen)
    • Iron deficiency

Treatment

Often, no treatment is required or necessary for reactive thrombocytosis.

However, in primary thrombocytosis, if platelet counts are over 750,000 or 1,000,000, and especially if there are other risk factors for thrombosis. Aspirin at low doses is thought to be protective, and extreme levels are treated with hydroxyurea (a cytoreducing agent). The new agent anagrelide (Agrylin®) has recently been introduced for the treatment of essential thrombocytosis. However, recent studies show that anegrilide is not significantly more effective than traditionally used hydroxyurea (Harrison et al 2005).

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Thrombocytosis
From Gale Encyclopedia of Medicine, 4/6/01 by Maureen Haggerty

Definition

Thrombocytosis is a blood disorder, in which the body produces a surplus of platelets (thrombocytes).

Description

Thrombocytosis is an abnormally increased number of platelets in the blood. Platelets are blood cells that stick together, helping blood clot. Thrombocytosis is a condition that may have many causes.

Throbocytosis is classified as one of two types. Secondary thrombocytosis can be traced to another cause, such as inflammation, severe bleeding, iron deficiency, or some cancers. Primary thrombocytosis (or essential thrombocythemia) is a single disease entity, with unique clinical characteristics.

Causes & symptoms

The cause of essential thrombocytosis is unknown.

Secondary thrombocytosis may develop as a result of:

  • Acute hemorrhage or infection
  • Anemia
  • Arthritis and other chronic inflammations
  • Cancer
  • Exercise
  • Iron deficiency
  • Medication
  • Osteoporosis
  • Removal of the spleen (splenectomy)
  • Polycythemia vera (a disorder affecting other red blood cells, as well as platelets)
  • Stress
  • Surgery.

Symptoms

Two of every three patients who have thrombocytosis do not have any symptoms of the disease at the time of diagnosis. Younger patients may remain symptom-free for years.

Enlargement of the spleen is detected in 60% of patients with thrombocytosis. The liver may also be enlarged. As many as half of all patients experience bleeding from the skin, gums, or nose, and 20-50% have some blockage of veins or arteries.

Other symptoms of thrombocytosis include:

  • Bloody stools
  • Bruising
  • Dizziness
  • Headache
  • Hemorrhage
  • Prolonged bleeding after having surgery or after having a tooth pulled
  • Redness or tingling of the hands and feet
  • Weakness. In rare instances, the lymph nodes become enlarged.

The highest platelet counts usually produce the most severe symptoms. Younger patients (especially women) may not have symptoms, even though their platelet counts are very high.

Complications

Complications of thrombocytosis include stroke, heart attack, and formation of blood clots in the arms and legs.

A doctor should be notified whenever bleeding is unexplained or prolonged or the patient develops:

  • Chest or leg pain
  • Confusion
  • Numbness
  • Weakness.

Diagnosis

The patient's symptoms suggest the presence of thrombocytosis. Blood tests confirm the diagnosis.

Bone marrow aspiration (removal of a tissue sample for microscopic examination) may also be performed.

Treatment

The key to treating secondary thrombocytosis is treating the underlying condition.

Any patient who has thrombocytosis should be encouraged not to smoke.

In young people who have no symptoms, this condition can remain stable for many years. These patients should be monitored by a physician, but may not require treatment.

Treatment for patients who do have symptoms focuses on controlling bleeding, preventing the formation of blood clots, and lowering platelet levels. Treatment for secondary thrombocytosis involves treating the condition or disease responsible for excess platelet production.

In 1997, the United States Food and Drug Administration (FDA) approved the use of anagrelide HCI (Agrylin) to reduce elevated platelet counts and decrease the risk of clot formation. Some patients have benefited from the use of hydroxyurea, an anti-cancer drug.

Low doses of aspirin may prevent clotting, but can cause serious hemorrhages.

If drug therapy does not bring platelet counts down to an acceptable level as rapidly as necessary, plateletpheresis may be performed. Usually combined with drug therapy and used primarily in medical emergencies, this procedure consists of:

  • Withdrawing blood from the patient's body
  • Removing platelets from the blood
  • Returning the platelet-depleted blood to the patient.

Prognosis

Many patients with thrombocytosis remain free of complications for long periods. However, some patients may die as a result of blood clots or uncontrolled bleeding.

Prevention

There is no known way to prevent thrombocytosis.

Further Reading

For Your Information

    Books

  • Berkow, Robert, ed. The Merck Manual of Medical Information: Home Edition. Whitehouse Station, NJ: Merck & Co., Inc., 1997.
  • Isselbacher, Kurt, J., et al, eds. Harrison's Principles of Internal Medicine. New York, NY: McGraw-Hill, Inc., 1994.

    Other

  • FDA Approves Marketing of Agrylin for Thrombocythemia. http://www.plsgroup.com.dg/2114a.htm (31 May 1998).
  • The Merck Manual: Primary Thrombocythemia. http://www.merck.com/!!ux1sK3PObux1sK3POb/pubs/mmanual/html/mjglmjdg.htm (3 June 1998).
  • Primary Thrombocythemia. http://www.healthanswers.com/database/ami/converted/000543.html (31 May 1998).

Gale Encyclopedia of Medicine. Gale Research, 1999.

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