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

Atopic eczema Allergic urticaria Allergic rhinitis Hay fever Allergic asthma Anaphylaxis Food allergy common allergies include: From Wikipedia, the free encyclopedia. Transfusion-associated graft versus host disease. Platelet transfusions may be performed in newborns, depending on the degree of thrombocytopenia. Nplate is an experimental treatment for stimulating platelet production.

Patient started treatment 7 years back and was on tablet isosorbide dinitrate 10 mg, tablet atenelol 25 mg, tablet envas 5 mg and patient had discontinued aspirin 6 months back. 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 less safe. Most cases respond during the 1 st purpurra of treatment.

The diagnosis of ITP is a diagnosis of exclusion. The patient was followed-up for 2 years and there was no re-occurence reported.

The mechanism of action of anti-D is not fully understood. Platelet transfusion is not normally recommended and is usually unsuccessful in raising a patient’s platelet count. However, while sometimes effective, it is costly and produces improvement that generally lasts less than a month.

Other biochemical examinations, liver function tests, and ultrasonography of abdomen were normal. Discussion There is marked variability in the clinical presentation of ITP. Children should be discouraged from rough contact sports or other activities that increase the risk of trauma. 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.

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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 ]. The major goal for treatment of ITP is to provide a safe platelet count to prevent major bleeding and avoid unnecessary treatment of asymptomatic patients with mild to moderate thrombocytopenia.

Bacterium eradication with antibiotics, in 12 of 13 infected patients The risk of neonatal tormbositopeni is increased with: A report of 66 cases. However, since the diagnosis depends on the exclusion of other causes of a low platelet count, additional investigations such as a bone marrow biopsy may be necessary in some cases.

At least 70 percent of childhood cases will end up in remission within six months, even without treatment. It is recommended that neonates be followed with serial platelet counts for the first few days after birth.

Patients are also advised to avoid using aspirin or ibuprofen as pain relievers because these drugs lengthen the clotting time of blood. Petechia, purpura, and easy bruising are expected in ITP. The clinical presentation may pyrpura acute with severe bleeding, or insidious with slow development with mild or no symptoms. Despite the destruction of platelets by splenic macrophages, the spleen is normally not enlarged. History of presenting illness revealed that patient noticed bleeding from his gums in lower front teeth region approximately 2 weeks before trombosiopeni to department and patient was having purpuric spots on body legs, hands, and neck since past 2 months.

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In adults, particularly those living in areas with a high prevalence trombositoleni 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. Later withdrawal of wysolone resulted in prupura relapse steroid dependant thrombocytopenia of another episode of melena.

Author information Copyright and Idkopatik information Disclaimer. Hypersensitivity and autoimmune diseases Endoscopy was performed again at the end of the treatment, which showed reduction in the fundal gastritis and absence of H.

Idiopathic thrombocytopenic purpura

ITP is usually chronic in adults [40] and the probability of durable remission is 20—40 percent. In a study conducted trombisitopeni Great Britainit was noted that ITP causes an approximately 60 percent higher rate of mortality compared to gender- and age-matched subjects without ITP.

A woman with symptomatic thrombocytopenia and an identifiable antiplatelet antibody should be started on therapy for their ITP which may include steroids or IVIG. CopyrightTiwari et al.

Hence one may be considered thrombocytopenic below that range, although the threshold for a diagnosis of ITP is not tied to any specific number. Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic. In conclusion, eradication of H. There is marked variability in the clinical presentation of ITP.