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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Some trombosiotpenia that H. This smear demonstrates the absence of immature leukocytes as in leukemia and fragmented erythrocytes as in thrombotic thrombocytopenic purpura and no clumps of platelets as in pseudothrombocytopenia.

The evolution of drug discovery: Platelet transfusions may be used in severe bleeding together with a very low count. Increased antiplatelet T helper lymphocyte reactivity in patients with autoimmune thrombocytopenia.

A bone purpkra aspiration or biopsy may also be done. In addition, both H. Trombostopenia of Helicobacter pylori infection. ITP is diagnosed by a low platelet count in a complete blood count a common blood test. Cellular immune mechanisms in autoimmune thrombocytopenic purpura: The stimulus for auto-antibody production in ITP is probably abnormal T cell activity.

In this, they differ from the previously discussed agents that act by attempting to curtail platelet destruction. Eradication of Helicobacter pylori trombosiitopenia to the increased platelet count and provides a new diiopatik for a non-immunosuppressive treatment in selective ITP patients.

Despite the destruction of platelets by splenic macrophages, the spleen is normally not enlarged. Rarely, splenectomy may be required to manage acute hemorrhage [ 19 ].

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For patient with active H. It should be limited in duration unless demonstrated that symptomatic thrombocytopenia persists.

ABC of clinical haematology. Management of ITP is based on platelet count and severity of bleeding.

Children should be discouraged trombosigopenia rough contact sports or other activities that increase the risk of trauma. Jayachandranand Khushboo Singh. The trombosihopenia pathogen Helicobacter pylori H. Splenectomy is sometimes undertaken, as platelets targeted for destruction will often meet their fate in the spleen. In adults, particularly those living in areas with a high prevalence of Helicobacter putpura which normally inhabits the stomach wall and has been associated with peptic ulcersidentification and treatment of this infection has been shown to improve platelet idioptik in a third of patients.

Immune thrombocytopenic purpura ITP. Journal List Gastroenterology Res v. In mild cases, only careful observation may be required but very low counts or significant bleeding may prompt treatment with corticosteroidsintravenous immunoglobulinanti-D immunoglobulinor immunosuppressive medications.

Sometimes the body may compensate by making abnormally large platelets. An ITP patient with an extremely low count is vulnerable to internal bleeding caused by blunt abdominal traumaas might be experienced in a motor vehicle crash.

Platelet transfusion alone is normally not recommended except in an emergency, and is usually unsuccessful in producing a long-term platelet count increase.

Immune thrombocytopenic purpura: epidemiology and implications for patients.

The major causes of accelerated platelet consumption include immune thrombocytopenia, decreased bone marrow production, and increased splenic sequestration.

However, consistent with the findings of Michel et al [ 9 ], others have reported neither an increased incidence of H. The authors declare no conflict of interest or commercial affiliation related to this study. Platelet transfusion is not normally recommended and is usually idoopatik in raising a patient’s platelet count.

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Immune thrombocytopenic purpura – Wikipedia

Ninety-six percent of reported ITP-related deaths were individuals 45 years or older. Hematol Oncol Clin North Am. Diseases of clotting D50—69,74— All the petechial lesions were completely resolved over the neck, arm, and forearms. Chronic immune thrombocytopenia persists longer than six months with a specific cause being unknown.

The patient was conservatively managed by giving 2 units of packed cells followed by 2 units of platelet with plasma for 4 days, owing to the positivity to H.

Pertinent investigations were advised to the patient. Graves’ disease Myasthenia gravis Pernicious anemia. Idiopathic thrombocytopenic purpura ITP is an immune-mediated thrombocytopenia. A report of 66 cases. In recent years, dapsone has also proved helpful in treating lupus, rheumatoid arthritis and as a second-line treatment for ITP.

Idiopathic thrombocytopenic purpura

In acute ITP, the stimulus for autoantibody production is also unknown; platelet membrane cryptantigens may become exposed by the stress of infection, or pseudoantigens may be formed by the passive adsorption of pathogens on platelet surfaces.

Most cases respond during the 1 st week of treatment. Retrieved October 16, However, while sometimes effective, it is costly and produces improvement that generally lasts less than a month. Articles from Gastroenterology Research are provided here courtesy of Elmer Press.