IDIOPATIK TROMBOSITOPENIA PURPURA PDF

1 Feb Read our article and learn more on MedlinePlus: Idiopathic thrombocytopenic purpura (ITP). Idiopathic thrombocytopenic purpura (ITP) is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. Idiopathic thrombocytopenic purpura (ITP) or immune thrombocytopenic purpura is a disease .. Purwanto I. Purpura trombositopenia idiopatik. In: Sudoyo AW.

Author: Kanris Kazilkis
Country: Dominica
Language: English (Spanish)
Genre: Finance
Published (Last): 24 September 2018
Pages: 249
PDF File Size: 2.66 Mb
ePub File Size: 16.33 Mb
ISBN: 689-7-98888-873-7
Downloads: 21024
Price: Free* [*Free Regsitration Required]
Uploader: Gugul

Immune thrombocytopenic purpura – Wikipedia

Idiopatik trombositopenia purpura the disease does not get better with prednisone, other treatments may hrombositopenia Bleeding complications in immune thrombocytopenia. Bleeding into the brain may also occur. Rituximab chimeric anti-CD20 monoclonal antibody treatment for adult refractory idiopathic thrombocytopenic purpura.

A prospective, randomized trial of high-dose intravenous immune globulin G therapy, oral prednisone therapy, and no idiopatik trombositopenia purpura in childhood acute immune thrombocytopenic purpura. Cellular isiopatik mechanisms in autoimmune thrombocytopenic purpura: Side effects of thrombopoietin receptor agonists include headache, joint or muscle pain, dizziness, nausea or vomiting, and an increased risk of idiopatik trombositopenia purpura clots.

Peripheral blood smear from a patient with immune thrombocytopenic purpura ITP shows a decreased number of platelets, a normal-appearing neutrophil, and normal-appearing erythrocytes.

Idiopathic Thrombocytopenic Purpura (ITP) in Emergency Medicine

Relative marrow failure may contribute to this condition, since studies show that most patients have either normal or diminished platelet production. Idiopathic thrombocytopenic purpura Idiopatik trombositopenia purpura is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause.

Aphthous stomatitis oral candidiasis lichen planus leukoplakia pemphigus vulgaris mucous membrane pemphigoid cicatricial pemphigoid herpesvirus coxsackievirus syphilis systemic histoplasmosis squamous-cell carcinoma.

On complete blood cell count, isolated thrombocytopenia is the hallmark of ITP. Foreign Hemolytic disease of the newborn. In adults, the peak prevalence is from years of age. High-dose intravenous gammaglobulin for idiopathic thrombocytopenic purpura in childhood.

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 bone marrow to make more platelets People idiopatik trombositopenia purpura ITP should not take aspirin, ibuprofen, or warfarin, because these drugs idiopatik trombositopenia purpura with platelet function or blood clotting, and bleeding may occur.

In adults, it is more often a long-term chronic disease and can occur after a viral infection, with use of certain idiopatik trombositopenia purpura, during pregnancy, or as part of an immune disorder. Novel approaches to refractory immune thrombocytopenic purpura.

/INSERT}

{INSERT-2-3}

However, other drug treatments are usually recommended instead. It is more common in children than adults. If bone marrow megakaryocytes cannot increase production and idiopatik trombositopenia purpura a normal number of circulating platelets, thrombocytopenia and purpura develop. In children, the disease usually goes away without treatment. Diabetes mellitus type 1 Hashimoto’s thyroiditis Multiple sclerosis Coeliac disease Giant-cell arteritis Postorgasmic illness syndrome Reactive arthritis.

Findings on peripheral blood smear are as follows:. Thrombocytopenia idiopatik trombositopenia purpura HIV infection: Platelet antibody testing in idiopathic idiopatik trombositopenia purpura purpura.

Platelets help your blood clot by clumping together to plug small holes in damaged blood vessels. Hemorrhage represents the most serious complication; intracranial hemorrhage is the most significant. Introduction Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic. Share Email Print Feedback Close. Share cases and questions with Physicians on Medscape consult.

The major causes of accelerated platelet consumption include immune thrombocytopenia, decreased bone marrow production, and increased splenic sequestration. Frederiksen H, Schmidt K. Medeiros D, Buchanan GR.

Adults are usually started on a steroid medicine called prednisone.

Idiopathic thrombocytopenic purpura

International consensus idipoatik on the investigation idiopatik trombositopenia purpura management of primary immune thrombocytopenia. ITP affects women idiopatik trombositopenia purpura often than men. In persons with ITP, platelets are coated with autoantibodies to platelet membrane antigens, resulting in splenic sequestration and phagocytosis by mononuclear macrophages.

This is because the underlying autoimmune mechanism that destroyed the patient’s platelets to begin with will also destroy donor platelets.

Health Topics A-Z Read more.

/INSERT}

{INSERT-2-3}

idiopatik trombositopenia purpura N Engl J Med. Treating immune thrombocytopenic purpura and preventing Rh alloimmunization using intravenous rho D immune globulin. Therefore, the former designation of reticuloendothelial system is considered imprecise. SlideShare Explore Search You.

/INSERT}

{INSERT-2-3}

J Pediatr Hematol Oncol. Anti-D immunoglobulin treatment for thrombocytopenia associated with primary antibody deficiency. With treatment, the idiopatik trombositopenia purpura of remission a symptom-free period is good. All the petechial lesions were completely resolved over the neck, arm, and forearms.