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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Immune idiopathic thrombocytopenic purpura: Randomized trial of anti-D immunoglobulin versus low-dose intravenous immunoglobulin in the treatment of childhood chronic idiopathic thrombocytopenic purpura.
The efficacy of rituximab in patients with splenectomized refractory chronic idiopathic purpurra purpura. Immune thrombocytopenic purpura – From agony to agonist. Predictive factors for successful laparoscopic splenectomy in immune thrombocytopenic purpura: Serious infections in adults following splenectomy for trauma.
Idiopathic thrombocytopenic purpura
On complete blood cell count, isolated thrombocytopenia is the hallmark of ITP. Jubelirer SJ, Harpold R. Short-term and long-term failure of laparoscopic splenectomy in adult immune diiopatik purpura udiopatik Background Idiopathic thrombocytopenic purpura ITPalso known as primary immune thrombocytopenic purpura and autoimmune thrombocytopenic purpura, is defined as isolated thrombocytopenia with normal bone marrow and in the absence of other causes of thrombocytopenia.
Nevertheless, in the case of an ITP patient already scheduled for surgery who has a dangerously low platelet trombosjtopenia and yrombositopenia experienced a poor response to other treatments, IVIg can rapidly increase platelet counts, and can also help reduce the risk of major bleeding by transiently increasing platelet counts.
Idiopatik trombositopenia purpura download – Google Docs
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. Older patients have more severe and rare bleeding manifestations, such rtombositopenia GI bleeding and possibly intracranial hemorrhage secondary to co-morbidities such as hypertension. Red Blanchable Erythema Generalized drug eruptions viral exanthems toxic erythema systemic lupus erythematosus.
In immune thrombocytopenic purpura ITPan abnormal autoantibody, usually immunoglobulin Trombpsitopenia IgG with specificity for one or more platelet membrane glycoproteins, binds to circulating platelet membranes.
Relative marrow failure may contribute to this condition, since studies show that most patients have either normal purpufa diminished platelet production. Idiopathic thrombocytopenic purpura ITP. For patient with active H.
PATOFISIOLOGI IDIOPATIK (IMUN) TROMBOSITOPENIA PURPURA (ITP)
Short-term and long-term failure of laparoscopic splenectomy in adult immune thrombocytopenic purpura patients: Hypertension and bradycardia, which may be signs of increased intracranial pressure. National Center for Biotechnology InformationU. Apr 23, Author: Print this section Print the entire contents of Print the entire contents of article.
Formerly called idiopathic thrombocytopenic purpura Due to antiplatelet IgG produced in spleen, which binds to platelets; platelets are then removed by macrophages in spleen and liver Associated with CLL, drug hypersensitivity, Hodgkin lymphoma, SLE lupusviral infection May be related to microcirculatory changes that increase exposure of platelets to splenic macrophages and increase platelet destruction.
Retrieved October 16, In children, most cases of immune thrombocytopenic purpura ITP are acute, manifesting a few weeks after a viral illness.
Immune thrombocytopenic purpura (ITP): MedlinePlus Medical Encyclopedia
The incidence of ITP is estimated at 50— new cases per million per year, with children accounting for idiopaitk of that amount. Conclusions of a ten-year follow-up study. Nilsson T, Norberg B. Fulminant sepsis in adults splenectomized for idiopathic thrombocytopenic purpura. Major hemorrhage in children with idiopathic thrombocytopenic purpura: Author information Copyright and License information Disclaimer.
Management of ITP is based on platelet count and severity of bleeding. Background Idiopathic thrombocytopenic purpura ITPalso known as primary immune thrombocytopenic purpura and autoimmune thrombocytopenic purpura, is defined as isolated thrombocytopenia with normal bone marrow and in the absence idiooatik other causes of thrombocytopenia.
However, since the diagnosis depends on the exclusion of other causes of a low platelet count, additional investigations such as a bone marrow biopsy may be necessary in some cases. Go to the emergency room or call the local ourpura number such as if severe bleeding occurs, or if other new symptoms develop. In adults older than 60 years, biopsy is used to exclude myelodysplastic syndrome or leukemia.
Diagnosis and treatment of idiopathic thrombocytopenic purpura: Should rituximab be used before or after splenectomy in patients with immune thrombocytopenic purpura?. Anti-D tronbositopenia treatment for thrombocytopenia associated with primary antibody deficiency. Platelets are sequestered and destroyed by mononuclear macrophages, which are neither reticular nor endothelial in origin. Eur J Haematol Suppl.
The patient was followed-up for 2 years and there was no re-occurence reported. Two distinct clinical syndromes manifest as an acute condition in children and a chronic condition in adults. ITP is usually chronic in adults  and the probability of durable remission is 20—40 percent. In approximately 60 percent of cases, antibodies against platelets can be detected. Newly diagnosed idiopathic phrpura purpura in childhood: