Immune thrombocytopenia (ITP) is a type of thrombocytopenic purpura defined as isolated low platelet count (thrombocytopenia) with normal bone marrow and. Amaç: İdiopatik trombositopenik purpura (ITP); trombositopenî, trombosit ömründe kısalma, plazmada anti-trombosit antikorların varlığı ve kemik iliğinde. Immune thrombocytopenic purpura (ITP) is a bleeding disorder in which the immune system destroys platelets, which are necessary for normal.

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Views Read Edit View history. The acute form often follows an infection and has a spontaneous resolution within two months. Another option, suitable for Rh-positive patients with functional spleens is intravenous administration of Rho D immune globulin [Human; Anti-D]. Cellular immune mechanisms in autoimmune thrombocytopenic purpura: Refractory ITP not responsive to conventional treatment may require splenectomythe surgical removal of the spleen.

All the petechial lesions were completely resolved over the neck, arm, and forearms. Current guidelines recommend treatment only in cases of significant bleeding. The treatment begins with IV steroids methylprednisolone or prednisoneIVIg or their combination and sometimes platelet infusions in order to raise the count quickly.

At least 70 percent of childhood cases will end up in remission within six months, even without treatment.


Petechial spots on dorsum of tongue, petechial spot on left side hard palate and left maxillary tuberosity region. Open in a separate window.

National Heart, Lung, and Blood Institute — www. Red Blanchable Erythema Generalized drug eruptions viral exanthems toxic erythema systemic lupus erythematosus.

Immune thrombocytopenic purpura (ITP): MedlinePlus Medical Encyclopedia

Splenectomy is sometimes undertaken, as platelets iidiopatik for destruction will often meet their fate in the spleen. Eltrombopag for the treatment of chronic idiopathic thrombocytopenic purpura.

Chemistry of Plants That Changed the World. Diagnosis and treatment of idiopathic thrombocytopenic purpura: Retrieved from ” https: In children, the disease affects boys and girls equally. Many older recommendations suggested a certain platelet count threshold usually somewhere below Bleeding time is usually prolonged.

ITP occurs when certain immune system cells produce antibodies against platelets. The stimulus for auto-antibody production in ITP is probably abnormal T cell activity. From Wikipedia, the free encyclopedia. This article has been cited by other articles in PMC.

Idiopathic thrombocytopenic purpura

The procedure is potentially risky in ITP cases due to the increased possibility of idiiopatik bleeding during surgery. Older patients have more severe and rare bleeding manifestations, such as GI bleeding and possibly intracranial hemorrhage secondary to co-morbidities such as hypertension.


Petechiae, or small bruise-like markings, may ieiopatik in ITP. Side effects of thrombopoietin receptor agonists include headache, joint or muscle pain, dizziness, nausea or vomiting, and an increased risk of blood clots. Foreign Hemolytic disease of the newborn. ITP symptoms can include any of the following: The antibodies attach to the platelets.

The bleeding manifestations of thrombocytopenia are described as mucocutaneous to distinguish them from coagulation disorders like hemophilia.

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It is recommended that neonates be followed with serial platelet counts for the first few days after birth. Basic Principles and Practice. Freckles lentigo melasma trmbosit melanoma. Graves’ disease Myasthenia gravis Pernicious anemia. In this, they differ from the previously discussed agents that act by attempting to curtail platelet destruction.

Spontaneous remissions are unusual in adults. Goldman L, Schafer AI, eds.