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). 23 Feb Idiopathic thrombocytopenic purpura (ITP) or immune thrombocytopenic purpura is a disease Purwanto I. Purpura trombositopenia idiopatik.

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Patient was admitted in Hematology Ward, Government General Hospital, Chennai on and treatment was started as described below: ITP affects women more often than men. Platelet transfusion alone is normally not recommended except in an emergency, and is usually unsuccessful in producing a long-term platelet count increase.

Foreign Allergic contact dermatitis Mantoux test. The procedure is potentially risky in ITP cases due trrombositopenia the increased possibility of significant bleeding during surgery. ITP has two distinct clinical syndromes, manifesting as an acute condition in children and a chronic condition in adults.

Share Email Print Feedback Close. Footnotes Source of Support: What would you like to print? Past medical history revealed that patient was known case of epilepsy since 7 years of age and was on tablet eptoin, tablet carbamazepine for past 12 years. Accessed November 9th, At least 70 percent of childhood cases will end up in remission within six months, even without treatment.

Keywords Idiopathic thrombocytopenic purpura; antiplatelet; antibodies; splenectomy; thrombopoietin. On the 2 nd day after the patient reported, puroura was increased bleeding, hematoma and gingival enlargement in lower anterior region [ Figure 4 ], and on the 4 th day, hematoma formation was seen in lower anterior region lingually [ Figure 5 ]. Epidemiology Frequency United States. Frederiksen H, Schmidt Trombisitopenia. Blood tests will be done to check your platelet count. The efficacy of rituximab in patients trojbositopenia splenectomized refractory chronic idiopathic thrombocythopenic purpura.


The pathophysiology of ITP revisited: Many older recommendations suggested a certain platelet count threshold usually somewhere below Bleeding into the brain may also occur.

In adults, the peak prevalence is from years of age. Author information Copyright and License information Disclaimer. ABC of clinical haematology. New cases of chronic refractory ITP comprise approximately 10 cases per 1, per year.

Idiopathic thrombocytopenic purpura

Therefore, ITP is a significant cause of fetal and neonatal immune thrombocytopenia. Share cases and questions with Physicians on Medscape consult. Thrombocytopenia caused by immunologic platelet destruction. Bleeding complications in immune thrombocytopenia. Rituximab and dexamethasone vs dexamethasone monotherapy in newly diagnosed patients with primary immune thrombocytopenia.

Elusive Remission Issues in Thrombocytopenia: The spleen and splenectomy in immune idiopathic thrombocytopenic purpura. Management of adult idiopathic thrombocytopenic purpura. Platelet activation in Helicobacter pylori-associated idiopathic thrombocytopenic purpura: Retrieved from ” https: Our case was abrupt and acute in onset. On fundoscopic examination, blurring of the optic disc margins udiopatik retinal hemorrhage.

The morphology of platelets is typically normal, with varying numbers of large platelets. National Heart, Lung, and Blood Institute — www.


The mortality rate due to chronic ITP varies but tends to be higher relative to the general population for any age range.

Immune Thrombocytopenic Purpura (ITP)

Immune idiopathic thrombocytopenic purpura: Initial laboratory findings useful for predicting the diagnosis of idiopathic thrombocytopenic purpura. Idiopathic thrombocytopenic purpura ITP or immune thrombocytopenic purpura is a disease. Practice Essentials Immune thrombocytopenic purpura ITP is a clinical syndrome in which a decreased number of circulating platelets thrombocytopenia see the image below manifests as a bleeding tendency, easy bruising purpuraor extravasation of blood from capillaries into skin and mucous membranes petechiae.

Postsplenectomy recurrence of thrombocytopenia with an accessory spleen. Share Email Print Feedback Close.

In this, they differ from the previously discussed agents that act by attempting to curtail platelet destruction.

If most of the platelets are large, approximating the diameter of red blood cells, or if they lack trombositopehia or have an abnormal color, consider an inherited platelet disorder. ITP occurs when certain immune system cells produce antibodies against platelets. Should rituximab be used before or after splenectomy in patients with immune thrombocytopenic purpura?. Other biochemical examinations, liver function tests, and ultrasonography of trombositopemia were normal.

Sign Up It’s Free! Pathogenesis of immune thrombocytopenia.

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