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) or immune thrombocytopenic purpura is a disease .. Purwanto I. Purpura trombositopenia idiopatik. In: Sudoyo AW. Idiopathic thrombocytopenic purpura (ITP) or immune thrombocytopenic purpura is a disease Purwanto I. Purpura trombositopenia idiopatik.

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The decision to treat ITP is based on the platelet count, degree of bleeding, and patient’s lifestyle. Acute primary ITP is more common in children years of age, with similar incidence between males and females, while the chronic form is usually encountered in adults with median age of years. Treatment should be restricted to those patients with moderate or severe thrombocytopenia who are bleeding or at risk of bleeding.


Immune thrombocytopenic purpura – From agony to agonist. Based on the clinical findings, provisional diagnosis was made as ITP.

Eur J Haematol ; Immune thrombocytopenic purpura ITP is a bleeding disorder in which the immune system destroys platelets, which are necessary for normal blood clotting.

In a fifth, the platelet count normalized completely; this response idioptik is similar to that found in treatment with rituximab, which is more expensive and less safe.


Br J Haematol ; With rare exceptions, there is usually no need to treat based on platelet counts. This website also contains material copyrighted by 3rd parties.

Identifying drugs that cause acute thrombocytopenia: Diseases of the skin and appendages by morphology. In chronic refractory cases, where immune pathogenesis has been confirmed, [15] the off-label use of the vinca alkaloid [16] [17] [18] and chemotherapy agent vincristine may be attempted. Current guidelines recommend treatment only in cases of significant bleeding. This is because the underlying autoimmune mechanism that is destroying the patient’s platelets will also destroy donor platelets, and so platelet transfusions are not considered a long-term treatment option.

Corticosteroids, typically prednisone, are the backbone of the initial treatment. The pathophysiology of ITP revisited: The treatment begins with IV steroids methylprednisolone or prednisoneIVIg or their combination and sometimes platelet infusions in order to raise the count quickly. 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.

Hematol Oncol Clin North Am. ITP is usually chronic in adults [40] and the probability of durable remission is 20—40 percent.

Immune thrombocytopenic purpura (ITP)

Dapsone also called diphenylsulfone, DDS, or avlosulfon is an anti-infective sulfone drug. There is marked variability in the clinical presentation of ITP. From Wikipedia, the free encyclopedia. Trombositkpenia mild cases, only careful observation may idiopatlk required but very low counts or significant bleeding may prompt treatment with corticosteroidsintravenous immunoglobulinanti-D immunoglobulinor immunosuppressive medications.


The major causes of accelerated platelet consumption include immune thrombocytopenia, decreased bone marrow production, and increased splenic sequestration. Please review our privacy policy. prupura

Idiopathic thrombocytopenic purpura

All the petechial lesions were completely resolved over the neck, arm, and forearms. ITP affects women more often than men. Thrombocytopenia caused by immunologic platelet destruction. Idiopathic thrombocytopenic purpura ITP is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. Bleeding time from minor lacerations or abrasions is usually prolonged. The clinical signs of ITP are purpura, ecchymosis, petechiae and gastrointestinal tract bleeding, gingival bleeding, epistaxis, and urinary tract bleeding.

Tromnositopenia older recommendations suggested a certain platelet count threshold usually somewhere below Infobox medical condition new All articles lacking reliable references Articles lacking reliable references from July This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.

Hemolytic disease of the newborn. J Thromb Haemost ;4: