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Immune Thrombocytopenic Purpura



Introduction: Immune Thrombocytopenic Purpura

Immune Thrombocytopenic Purpura: Immune refers to the immune system's involvement in this disorder. Antibodies, part of the body's immunologic defense against infection, ... more about Immune Thrombocytopenic Purpura.

Immune Thrombocytopenic Purpura: Reduced blood platelets causing visible skin blemishes from bleeding or bruising. More detailed information about the symptoms, causes, and treatments of Immune Thrombocytopenic Purpura is available below.

Symptoms of Immune Thrombocytopenic Purpura

See full list of 11 symptoms of Immune Thrombocytopenic Purpura

Home Diagnostic Testing

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Medical Textbooks Online about Immune Thrombocytopenic Purpura

Medical Books Excerpts
  • "Algorithmic Diagnosis of Symptoms and Signs"
  • "Algorithmic Diagnosis of Symptoms and Signs"
  • "In a Page: Signs and Symptoms"
  • "In A Page: Pediatric Signs and Symptoms"
  • "In A Page: Pediatric Signs and Symptoms"
  • "Differential Diagnosis in Primary Care"
  • "Handbook of Signs & Symptoms (Third Edition)"
  • "A Pocket Manual of Differential Diagnosis"
  • "A Pocket Manual of Differential Diagnosis"
  • "Professional Guide to Diseases (Eighth Edition)"
  • "Professional Guide to Diseases (Eighth Edition)"
  • "Professional Guide to Diseases (Eighth Edition)"
  • "Professional Guide to Diseases (Eighth Edition)"
  • "Professional Guide to Signs & Symptoms (Fifth Edition)"
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter"
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter"
  • "Field Guide to Bedside Diagnosis"
  • "Handbook of Diseases"
  • "Handbook of Diseases"
  • "Handbook of Diseases"
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses"
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics"
  • "Nursing: Interpreting Signs and Symptoms"

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Diagnostic Tests for Immune Thrombocytopenic Purpura

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Wrongly Diagnosed with Immune Thrombocytopenic Purpura?

Misdiagnosis and Immune Thrombocytopenic Purpura

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Causes of Immune Thrombocytopenic Purpura

Read more about causes of Immune Thrombocytopenic Purpura

More information about causes of Immune Thrombocytopenic Purpura:

Treatments for Immune Thrombocytopenic Purpura

See full list of 14 treatments for Immune Thrombocytopenic Purpura

Videos for Immune Thrombocytopenic Purpura

Rituxan: NHL Treatment

Rituxan: NHL TreatmentIn recent years, the drug Rituxan has become a well-established option only for certain forms of non-Hodgkin's lymphoma (NHL) There are other...

 
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Patient Surveys for Immune Thrombocytopenic Purpura

Prognosis for Immune Thrombocytopenic Purpura

Prognosis for Immune Thrombocytopenic Purpura: Acute ITP: 85% of children recover within 1 year and have no remissions.

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Statistics for Immune Thrombocytopenic Purpura

Types of Immune Thrombocytopenic Purpura

  • Idiopathic Immune Thrombocytopenic Purpura - of unknown cause.
  • Secondary Immune Thrombocytopenic Purpura - caused by some other condition.
  • Acute thrombocytopenic purpura - usually temporary
  • Chronic thrombocytopenic purpura - lasting more than 6 months.

Read more about Types of Immune Thrombocytopenic Purpura

Stories from Users Related to Immune Thrombocytopenic Purpura

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Article Excerpts about Immune Thrombocytopenic Purpura

Immune refers to the immune system's involvement in this disorder. Antibodies, part of the body's immunologic defense against infection, attach to blood platelet, cells that help stop bleeding, and cause their destruction. Thrombocytopenia refers to decrease in blood platelet. Purpura refers to the purplish- looking areas of the skin and mucous membranes (such as the lining of the mouth) where bleeding has occurred as a result of decreased platelet. (Source: excerpt from Immune Thrombocytopenic Purpura (ITP): NIDDK)

Definitions of Immune Thrombocytopenic Purpura:

Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. - (Source - Diseases Database)

Immune Thrombocytopenic Purpura is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Immune Thrombocytopenic Purpura, or a subtype of Immune Thrombocytopenic Purpura, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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