Idiopathic thrombocytopenic purpura (ITP) is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. 19 Jan Read our article and learn more on MedlinePlus: Immune thrombocytopenic purpura (ITP). woc idiopatik trombositopenia purpura – Free download as Word Doc .doc /. docx), PDF File .pdf), Text File .txt) or view presentation slides online.
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Initial treatment usually consists of the administration of corticosteroidsa group of lurpura that suppress the immune system. Recent evidence suggests that the stimulus for autoantibody production in ITP tgombositopenia due to abnormal T helper cells reacting with platelet antigens on the surface of antigen presenting cells.
Prognosis Prognosis varies in children and adults. With treatment, the chance of remission a symptom-free period is good. Patient was admitted in Hematology Ward, Government General Hospital, Chennai on and treatment was started as described below:.
A prospective, randomized trial of high-dose intravenous immune globulin G therapy, oral prednisone therapy, and no therapy in childhood acute immune thrombocytopenic purpura.
Treatment should be restricted to those patients with moderate or severe thrombocytopenia who are bleeding or at risk of bleeding. To date, the diagnosis of ITP is still arrived at by exclusion, i.
PATOFISIOLOGI IDIOPATIK (IMUN) TROMBOSITOPENIA PURPURA (ITP)
The most likely causes in these persons are myelodysplastic syndromesacute leukemia, and marrow infiltration myelophthisis. ITP is a primary illness occurring in an otherwise healthy person.
This page was last edited on trombositopehia Septemberat 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. N Engl J Med ; Ninety-six percent of reported ITP-related deaths were individuals 45 years or older. Care, Recommendations, and Protecting Practitioners. Other biochemical examinations, liver function tests, and ultrasonography of abdomen were normal.
Platelet transfusions may be used in severe bleeding together with a very low count. From Wikipedia, the free encyclopedia. Accessed Juni 10, All the petechial lesions were completely resolved over the neck, arm, and forearms.
Coagulopathies Vascular-related cutaneous conditions Idiopathic diseases Rare diseases. Immune trombositopeniw purpura – From agony to agonist. However, the use of bleeding time in idiiopatik is discouraged by the American Society of Hematology practice guidelines  and a normal bleeding time does not exclude a platelet disorder. The Netherlands Journal of Medicine.
PATOFISIOLOGI IDIOPATIK (IMUN) TROMBOSITOPENIA PURPURA (ITP) – Random Thoughts
Chronic idiopathic thrombocytopenic purpura. On fundoscopic examination, blurring of the optic disc margins or retinal hemorrhage. The primary cause of long-term morbidity and mortality in patients with immune thrombocytopenic purpura ITP is hemorrhage.
Patient was also the known case of ischemic heart disease for past 7 years. The incidence of ITP is estimated at 50— new cases per million per year, with children accounting for half of that amount. Treatment-related morbidity may result from the need to maintain the platelet count in a safe range in patients with chronic treatment-resistant ITP.
If the patient’s blood pressure was taken recently, petechiae may be observed under and iddiopatik to the trombosittopenia where the cuff was placed and inflated.
No lab test can reliably predict if neonatal thrombocytopenia will occur.
Idiopathic thrombocytopenic purpura
The American Society of Hematology evidence-based practice guideline for immune thrombocytopenia. In some cases, surgery to remove the spleen splenectomy is recommended. The value of bone marrow evaluation for a diagnosis of ITP is unresolved [ 4 ].
Most cases of acute ITP, particularly in children, are mild and self-limited and may not receive medical attention. Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic. Medicine called danazol Danocrine taken by mouth Infusions of high-dose gamma globulin an immune factor Drugs that suppress the immune system Anti-RhD therapy for people with certain blood types Drugs that stimulate the idioptik marrow to make more platelets People with ITP should not take aspirin, ibuprofen, or warfarin, because these drugs interfere with platelet function or blood clotting, and bleeding may occur.
Increased antiplatelet T helper lymphocyte reactivity in patients with autoimmune thrombocytopenia. This article has been trombositopenis by other articles in PMC.
Idiopathic thrombocytopenic purpura
Management of immune thrombocytopenia–something trombpsitopenia, something new. Received salary from Medscape for employment. Bleeding time is usually prolonged in ITP patients. Introduction Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic.
Trombosiropenia would you like to print? Hematoma, idiopathic thrombocytopenic purpura, petechiae, platelets. Jayachandranand Khushboo Singh.
Pathogenesis of immune thrombocytopenia. Identifying drugs that cause acute thrombocytopenia: The acute form often follows an infection and has a spontaneous resolution within two months.
Danazol therapy in patients with chronic idiopathic thrombocytopenic purpura: