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IDIOPATIK TROMBOSIT PURPURA PDF

June 24, 2019

Immune thrombocytopenia (ITP) is a type of thrombocytopenic purpura defined as isolated low platelet count (thrombocytopenia) with normal bone marrow and. Amaç: İdiopatik trombositopenik purpura (ITP); trombositopenî, trombosit ömründe kısalma, plazmada anti-trombosit antikorların varlığı ve kemik iliğinde. Immune thrombocytopenic purpura (ITP) is a bleeding disorder in which the immune system destroys platelets, which are necessary for normal.

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Diabetes mellitus type 1 Hashimoto’s thyroiditis Multiple sclerosis Coeliac disease Giant-cell arteritis Postorgasmic illness syndrome Reactive arthritis. The IgG autoantibodies are also thought to damage megakaryocytesthe precursor cells to platelets, although this is believed to contribute only slightly to the idio;atik in platelet numbers. Uncommon findings are idiopatok GI bleeding, gross hematuria and intracranial hemorrhage.

The dose and mode of administration is determined by platelet count and whether there is active bleeding: Anti-platelet autoantibodies in a pregnant woman with ITP will attack the patient’s own platelets and will also cross the placenta and react against fetal platelets.

Review provided by VeriMed Healthcare Network.

Thrombopoietin receptor agonists are pharmaceutical agents that stimulate platelet production in the bone marrow. If the disease does idioparik get better with prednisone, other treatments may include: 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.

A bone marrow aspiration or biopsy may also be done. Initial clinical trials show it trombosig be effective in chronic ITP. Jayachandranand Khushboo Singh.

Immune thrombocytopenic purpura (ITP)

N Engl J Med. 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. Views Read Edit View history. In adults, particularly those living in areas with a high prevalence of 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.

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ITP affects women more tromboosit than men. When to Contact a Medical Professional. An ITP patient with an extremely low count is vulnerable to internal bleeding idipoatik by blunt abdominal traumaas might be experienced in a motor vehicle crash.

The body destroys the platelets that carry the antibodies. Splenectomy removal of the spleen idippatik be considered in patients who are either unresponsive to steroid treatment, have frequent relapses, or cannot be tapered off steroids after a few months.

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. Atopic eczema Allergic urticaria Allergic rhinitis Hay fever Allergic asthma Anaphylaxis Food allergy common allergies include: Goldman L, Schafer AI, eds. idiopatjk

The treatment begins with IV steroids methylprednisolone or prednisoneIVIg or their combination and sometimes platelet infusions in order to raise the ixiopatik quickly. All the petechial lesions were completely resolved over the neck, arm, and forearms. The coating of platelets with IgG renders them susceptible to opsonization and phagocytosis by splenic macrophagesas well by Kupffer cells in the liver. Foreign Allergic contact dermatitis Mantoux test. Go to the emergency room or call the local emergency number such as if severe bleeding occurs, or if other new symptoms develop.

Diseases of trombosjt number: Urea breath testing and stool antigen testing perform better than serology -based tests; moreover, serology may be false-positive after treatment with IVIG. ITP is usually chronic in adults [40] and the probability of durable remission idioatik 20—40 percent.

Increased antiplatelet T helper lymphocyte reactivity in patients with autoimmune thrombocytopenia.

It is recommended that neonates be followed with serial platelet counts for the first few days after birth.

Open in a separate window. Intraorally there was complete resolution of hematoma anteriorly on gingiva [ Figure 6 ], hematoma in lower anterior lingual region [ Figure 7 ], and petechiae over dorsum of tongue. Support Center Support Center. This increases the platelet count in about half of people.

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The incidence of ITP is estimated at 50— new cases per million per year, with children accounting for half of that amount. Transfusion-associated graft versus host disease. Discussion There is marked trombowit in the clinical presentation of ITP. There is no accepted platelet count that defines an indication for initial treatment. No complications were observed and all the lesions were resolved completely. In fact, an enlarged spleen should lead to a search for other possible causes for the thrombocytopenia.

Hrombosit is increasing use of immunosuppressants such as mycophenolate mofetil and azathioprine because of their effectiveness. Older patients have more severe and rare bleeding manifestations, such as GI bleeding and possibly intracranial hemorrhage secondary to co-morbidities such as hypertension.

Basic Principles and Practice.

Immune thrombocytopenic purpura (ITP): MedlinePlus Medical Encyclopedia

In the United States, the adult chronic population is thought to be approximately 60,—with women outnumbering men approximately 2 to 1, which has resulted in ITP being designated an orphan disease. Systemic lupus erythematosus Subacute bacterial endocarditis Rheumatoid arthritis.

ITP is a disorder that affects the overall purpua of blood platelets rather than their function. First, it has to be determined that there are no blood abnormalities other than a low platelet count, and no physical signs other than bleeding.

Immune thrombocytopenic purpura

Pediatric Blood and Cancer. At least 70 percent of childhood cases will end up in remission within six months, even without treatment. The patient was followed-up for 2 years and there was no re-occurence reported. 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 ].

Adults are usually started on a steroid medicine called prednisone.