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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Idiopathic thrombocytopenic purpura ITP is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. The major causes of accelerated platelet consumption include immune thrombocytopenia, decreased bone marrow production, and increased splenic sequestration.
The clinical presentation may be trombosiyopenia with severe bleeding, or insidious with slow development with mild or no symptoms.
Treatment should be restricted to those patients with moderate or severe thrombocytopenia who are bleeding or at risk of bleeding.
We present a case report on ITP with clinical presentation, diagnosis and management. Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic.
As most causes appear to be related to antibodies against platelets, it is also known as immune thrombocytopenic purpura. Although most cases are asymptomatic, very low platelet counts can lead to a bleeding diathesis and purpura.
ITP is a disorder that affects the overall number of blood platelets rather than their function. ITP may be either acute or chronic. The incidence of ITP is new cases per million per year, with children accounting for half of that amount and the median age of adults at the diagnosis is Recent evidence suggests that the stimulus for autoantibody production in ITP is due to abnormal T helper cells reacting with platelet antigens on the surface of antigen presenting cells.
The diagnosis of ITP is a diagnosis of exclusion. First, one has to make sure that there are no other blood abnormalities except for low platelet count and no physical signs except for signs of bleeding. Secondary causes could be leukemia, medications e.
The size and appearance of the platelets may be abnormal. Bleeding time is usually prolonged. Bleeding time is prolonged in ITP patients; however, the use of bleeding time in diagnosis is discouraged by the American Society of Hematology practice guidelines as useless.
On examination of the bone marrow, an increase in the production of megakaryotes is seen and can help in determining ITP. It should be limited in duration unless demonstrated that symptomatic thrombocytopenia persists. Patients with mild, asymptomatic thrombocytopenia, discovered incidentally on a routine blood count, should not be treated. History of presenting illness revealed that patient noticed bleeding from his gums in lower front teeth region approximately 2 weeks before reporting to department and patient was having purpuric spots on body legs, hands, and neck since past 2 months.
Past medical history revealed that patient was known case of epilepsy since 7 years of age and was on tablet purpuga, tablet carbamazepine for past 12 years. Patient was also the known case of ischemic heart disease for past 7 years. 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. 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 ].
Intraoral examination revealed bleeding from gingiva in lower anterior region, tromboeitopenia was inflamed, reddish, tender on palpation, soft in consistency [ Figure 3 ]. Petechial spots on dorsum of tongue, petechial spot on left side hard palate and left maxillary tuberosity region.
On the 2 nd day after the patient reported, there was increased bleeding, xdalah 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 ].
Based on the clinical findings, provisional diagnosis was made as ITP. Pertinent investigations were advised to the patient. Other biochemical examinations, liver function tests, and ultrasonography of abdomen were normal.
Immune thrombocytopenic purpura – Wikipedia
Patient was admitted in Hematology Ward, Government General Hospital, Chennai on and trombosifopenia was started as described below:. No complications were observed and all the lesions were resolved completely. All the petechial lesions were completely resolved over the neck, arm, and forearms.
Intraorally there was complete resolution of hematoma anteriorly on gingiva [ Figure 6 ], hematoma in lower anterior lingual trombosiotpenia [ Figure 7 ], and petechiae over dorsum of tongue. The patient was followed-up for 2 years and there was no re-occurence reported. There is marked variability in the clinical presentation of ITP. Our case was abrupt and acute in onset.
The bleeding manifestations of thrombocytopenia are described as mucocutaneous to distinguish them from coagulation disorders like hemophilia.
Immune thrombocytopenic purpura
Petechia, purpura, and easy bruising are expected in ITP. Less common are epistaxis, gingival bleeding, and menorrhagia. Uncommon findings are gastrointestinal GI bleeding, gross hematuria and intracranial hemorrhage. Older patients have more severe and rare bleeding manifestations, such as GI bleeding and possibly intracranial hemorrhage secondary to co-morbidities such as hypertension.
The diagnosis of ITP is in part one of exclusion, requiring that other causes of thrombocytopenia be ruled out. 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.
Spontaneous remissions are unusual in adults. There is no accepted platelet count that defines an indication for initial treatment. The decision to treat ITP is based on the platelet count, degree of bleeding, and patient’s lifestyle.
There is no specific treatment for ITP. General care includes explaining ITP to the patient and advising him or her to watch for bruising, petechiae, or other signs of recurrence.
Children should be discouraged from rough contact sports or other activities that increase the risk of trauma. Patients are also advised to avoid using aspirin or ibuprofen as pain relievers because these drugs lengthen the clotting time of blood. All medications for ITP are given either orally or IV; intramuscular injection is avoided due to the possibility of causing bleeding into the skin.
Corticosteroids, typically prednisone, are the backbone of the initial treatment. The treatment begins with IV steroids methylprednisolone or prednisoneIVIg or their combination and sometimes platelet infusions in order to raise the count quickly. Most cases respond during the 1 st week of treatment.
After several weeks of prednisone therapy, the dose is gradually reduced. Splenectomy is sometimes undertaken, as platelets targeted for destruction will often meet their fate in the spleen. Other immunosuppresants, which are steroid sparing drugs like mycophenolate mofetil and azathioprine, are becoming more popular for their effectiveness.
Platelet transfusion is not normally recommended and is usually unsuccessful in raising a patient’s platelet count. This is because the underlying autoimmune mechanism that destroyed the patient’s platelets to begin with will also destroy donor platelets. An exception to this rule is when a patient is bleeding profusely, when transfusion of platelets can quickly form a platelet plug to stop bleeding.
Dapsone also called diphenylsulfone, DDS, or avlosulfon is an anti-infective sulfone drug. In recent years, dapsone has also proved helpful in treating lupus, rheumatoid arthritis and as a second-line treatment for ITP. The exact mechanism by which dapsone assists in ITP is unclear.
Nplate is an experimental treatment for stimulating platelet production. It is a thrombopoiesis stimulating Fc-peptide fusion protein peptibody.
Initial clinical trials show it to be effective in chronic ITP. For patient with active H. The initial treatment of ITP includes: National Center for Biotechnology InformationU. Journal List Contemp Clin Dent v. Jayachandranand Khushboo Singh. Author information Copyright and License information Disclaimer. This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.
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Abstract Idiopathic thrombocytopenic purpura ITP is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. Hematoma, idiopathic thrombocytopenic purpura, petechiae, platelets.
Introduction Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic. Patient was admitted in Hematology Ward, Government General Hospital, Chennai on and treatment was started as described below: Open in a separate window. Discussion There is marked variability in the clinical presentation of ITP. Conclusion The initial treatment of ITP includes: Footnotes Source of Support: Nil Conflict of Interest: Management of adult idiopathic thrombocytopenic purpura.
Cellular immune mechanisms in autoimmune thrombocytopenic purpura: Immune thrombocytopenic purpura – From agony to agonist.
N Engl J Med. Semple JW, Freedman J. Increased antiplatelet T helper lymphocyte reactivity in patients with autoimmune thrombocytopenia. Diagnosis and treatment of idiopathic thrombocytopenic purpura: Recommendations of the American Society of Hematology. ABC of clinical haematology. Initial laboratory findings useful for predicting the diagnosis of idiopathic thrombocytopenic purpura.
Rituximab chimeric anti-CD20 monoclonal antibody treatment for adult refractory idiopathic thrombocytopenic purpura. Long-term responses seen with rituximab in patients with ITP. Dapsone for chronic autoimmune thrombocytopenic purpura: