IDIOPATIK TROMBOSITOPENI PURPURA PDF

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Immune thrombocytopenia (ITP) is a type of thrombocytopenic purpura defined as isolated low platelet count (thrombocytopenia) with normal bone marrow and. Idiopathic thrombocytopenic purpura (ITP) is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. Eur J Haematol Suppl. Mar;(71) doi: /j x. Immune thrombocytopenic purpura: epidemiology and implications for.

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General care includes explaining ITP to the patient and advising him or her to watch for bruising, petechiae, or other signs of recurrence.

Immune thrombocytopenic purpura

Recent evidence suggests that the stimulus for autoantibody production in ITP is due to abnormal T helper cells reacting with platelet antigens on the surface of antigen presenting cells. On examination of the bone marrow, an increase in the production of megakaryotes is seen and can help in determining ITP. It causes a characteristic purpuric rash and an increased tendency to bleed.

Helicobacter pylori and autoimmune neutropenia. Most cases respond during the 1 st week of treatment. Several studies have proposed that H. Older patients have more severe and rare bleeding manifestations, such as GI idiopatii and possibly intracranial hemorrhage secondary to co-morbidities such as hypertension.

The dose and mode of administration is determined by platelet count and whether there is active bleeding: Initial laboratory findings useful for predicting the diagnosis of idiopathic thrombocytopenic purpura. Many hypotheses have suggested that correlate H.

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Immune thrombocytopenic purpura: epidemiology and implications for patients.

Cellular immune mechanisms in autoimmune thrombocytopenic purpura: The bleeding manifestations of thrombocytopenia are described as mucocutaneous to distinguish them from coagulation disorders like hemophilia.

Studies of similar type may also be helpful in assessing the long lasting effect of anti- Ourpura. Pertinent investigations were advised to the patient.

Diseases of clotting D50—69,74— Please review our privacy policy. Two distinct clinical syndromes manifest as an trobmositopeni condition in children and a chronic condition in adults.

Corticosteroids, typically prednisone, are the backbone of the initial treatment. An analysis for anti-platelet antibodies is a matter of clinician’s preference, as there is disagreement on whether the 80 percent specificity of this test is sufficient to be clinically useful. In one of the small study by Trombosifopeni et al [ 6 ], which consisted of 30 subjects, H.

Chemistry of Plants That Changed the World. Despite the idiopatkk of platelets pkrpura splenic macrophages, the spleen is normally not enlarged. Systemic lupus erythematosus Subacute bacterial endocarditis Rheumatoid arthritis. Nil Conflict of Interest: Sometimes the body may compensate by making abnormally large platelets.

In a fifth, the platelet count normalized completely; this response rate is similar to that found in treatment with rituximab, which is more expensive and tromgositopeni safe. Foreign Allergic contact dermatitis Mantoux test. Introduction Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic. Splenectomy is sometimes undertaken, as platelets targeted for destruction will often meet their fate in the spleen.

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Patient was admitted in Hematology Ward, Government General Hospital, Chennai on and treatment was started idiooatik described below:. The major causes of accelerated platelet consumption include immune thrombocytopenia, decreased bone marrow production, and increased splenic sequestration.

The IgG autoantibodies are also thought to damage megakaryocytesthe precursor cells to platelets, although this is believed to contribute only slightly to the decrease in platelet numbers.

Immune thrombocytopenic purpura – Wikipedia

Platelet transfusions may be performed in newborns, depending on the degree of thrombocytopenia. This page was last edited on 27 Septemberat Spontaneous remissions are unusual in adults.

The size and appearance of the platelets may be abnormal.

There is increasing use of immunosuppressants such as mycophenolate mofetil and azathioprine because of their effectiveness.