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Thrombotic thrombocytopenic purpura

TTP

Thrombotic thrombocytopenic purpura (TTP) is a blood disorder in which platelet clumps form in small blood vessels. This leads to a low platelet count (thrombocytopenia).

Causes

This disease may be caused by problems with an enzyme (a type of protein) that is involved in blood clotting. This enzyme is called ADAMTS13. Absence of this enzyme results in platelet clumping. Platelets are particles in the blood that aid in blood clotting.

As the platelets clump together, fewer platelets are available in the blood in other parts of the body to help with clotting. This can lead to bleeding under the skin.

In some cases, the disorder is passed down through families (inherited). In these cases, people are born with naturally low levels of this enzyme.

This condition also may be caused by:

  • Cancer
  • Chemotherapy
  • Hematopoietic stem cell transplantation
  • HIV infection
  • Hormone replacement therapy and estrogens
  • Medicines (including ticlopidine, clopidogrel, quinine, and cyclosporine A)

Symptoms

Symptoms may include any of the following:

Exams and Tests

Tests that may be ordered include:

Treatment

You may have a treatment called plasma exchange. It removes your abnormal proteins in your plasma and replaces it with normal plasma from a healthy donor. Plasma is the liquid part of blood that contains blood cells and platelets. Plasma exchange also replaces the missing enzyme.

The procedure is done as follows:

  • First, you have your blood drawn as if donating blood.
  • As the blood is passed through a machine that separates blood into its different parts, the abnormal plasma is removed and your blood cells are saved.
  • Your blood cells are then combined with normal plasma from a donor, and then given back to you.

This treatment is repeated daily until blood tests show improvement.

People who do not respond to this treatment or whose condition often returns may need to:

  • Have surgery to remove their spleen
  • Get medicines that suppress the immune system, such as steroids or rituximab

Outlook (Prognosis)

Most people with TTP who undergo plasma exchange recover completely. But some people die of this disease, especially if it is not diagnosed right away. In people who do not recover, this condition can become long-term (chronic).

Possible Complications

Complications may include:

  • Kidney failure
  • Low platelet count (thrombocytopenia)
  • Low red blood cell count (caused by the premature breakdown of red blood cells)
  • Nervous system problems
  • Severe bleeding (hemorrhage)
  • Stroke

When to Contact a Medical Professional

Contact your health care provider if you have any unexplained bleeding.

Prevention

Because the cause is unknown, there is no known way to prevent this condition.

Open References

References

Abrams CS. Thrombocytopenia. In: Goldman L, Schafer AI, eds. Goldman-Cecil Medicine. 26th ed. Philadelphia, PA: Elsevier; 2020:chap 163.

George G, Friedman KD. Thrombotic thrombocytopenic purpura and the hemolytic uremic syndromes. In: Hoffman R, Benz EJ, Silberstein LE, Heslop HE, Weitz JI, Salama ME, et al, eds. Hematology: Basic Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 132.

National Heart, Lung, and Blood Institute website. Thrombotic thrombocytopenic purpura. www.nhlbi.nih.gov/health-topics/thrombotic-thrombocytopenic-purpura. Updated February 2023. Accessed March 9, 2023.

  • Blood cells

    Blood cells - illustration

    Blood is comprised of red blood cells, platelets, and various white blood cells.

    Blood cells

    illustration

  • Blood cells

    Blood cells - illustration

    Blood is comprised of red blood cells, platelets, and various white blood cells.

    Blood cells

    illustration

Tests for Thrombotic thrombocytopenic purpura

 
 

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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