IDIOPATIK TROMBOSITOPENI PURPURA PDF

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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Immune thrombocytopenic purpura – Wikipedia

Retrieved from ” https: Semple JW, Freedman J. Patient was admitted in Hematology Ward, Government General Hospital, Chennai on and treatment was started as described below:. The dose and mode of administration is determined by platelet count and whether there is active bleeding: Intraorally there was complete resolution of hematoma anteriorly on gingiva [ Figure 6 ], hematoma in lower anterior lingual region [ Figure 7 ], and petechiae over dorsum of tongue.

D ICD – This increased risk of death with ITP is largely concentrated in the middle-aged and elderly. Extraoral examination revealed petechial spots over the neck on right side [ Figure 1 ], petechial spots over the forearms, and petechial spots over the right arm [ Figure 2 ]. Refractory ITP not responsive to conventional treatment may require splenectomythe surgical removal of the spleen. The first case of association of H. Endoscopy was performed again at the end of the treatment, which showed reduction in the fundal gastritis and absence of H.

Autoimmune thrombocytopenic Purpura and Helicobacter pylori infection. A woman with symptomatic thrombocytopenia and an identifiable antiplatelet antibody should be started on therapy for their ITP which may include steroids or IVIG. The platelet count of the patient was monitored every fortnight and was found to be normal after completion of one-week anti- H. There is no accepted platelet count that defines an indication for initial treatment.

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Patient was also the known case of ischemic heart disease for past 7 years. In adults, particularly those living in areas with a high prevalence of Helicobacter pylori which normally inhabits the stomach wall and has been associated with peptic ulcersidentification and treatment of this infection has been shown to improve platelet counts in a third of patients.

There is no specific treatment for ITP. 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. Idiopathic thrombocytopenic purpura ITP is an immune-mediated thrombocytopenia. The bleeding manifestations of thrombocytopenia are described as mucocutaneous to distinguish them from coagulation disorders like hemophilia.

This is trombosiropeni open-access article puprura under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Allergic contact dermatitis Mantoux test.

Chronic immune thrombocytopenia persists longer than six months with a specific cause being unknown. First, it has to be determined that there are no blood abnormalities other than a low platelet count, and no physical signs other than bleeding. The risk of neonatal thrombocytopenia is increased with: The clinical presentation may be acute with severe bleeding, or insidious with slow development with mild or no symptoms.

Infobox medical condition new All articles lacking reliable references Articles lacking reliable references from July Patients are also advised to avoid using aspirin or ibuprofen as pain relievers because these drugs lengthen the clotting time of blood. Many hypotheses have suggested that correlate H.

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Immune thrombocytopenic purpura: epidemiology and implications for patients.

Intraoral examination revealed bleeding from gingiva in lower anterior region, which was inflamed, reddish, tender on palpation, soft in consistency [ Figure 3 ].

The mechanism of action of anti-D is not fully understood.

Pathogenesis of Helicobacter pylori infection. British Journal of Haematology.

Immune thrombocytopenic purpura: epidemiology and implications for patients.

The procedure is potentially risky in ITP cases due to the increased possibility of significant bleeding during surgery. This page was last edited on 27 Septemberat Secondary causes could be leukemia, medications e. Treatment should be restricted to those patients with moderate or iddiopatik thrombocytopenia who are bleeding or at risk of bleeding. Uncommon findings are gastrointestinal GI bleeding, gross hematuria and intracranial hemorrhage.

After several weeks of prednisone therapy, the dose is gradually reduced. In fact, an enlarged spleen should lead to a search for other possible causes for the thrombocytopenia. ABC of clinical haematology.

Idiopathic thrombocytopenic purpura

Long-term responses seen with rituximab in patients with ITP. Ninety-six percent of reported ITP-related deaths were individuals 45 years or older. History of presenting illness revealed that patient noticed bleeding from his gums in lower front purura region approximately 2 weeks before reporting to department and patient was having purpuric spots on body legs, hands, and neck since past 2 months.

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