نتایج جستجو برای: autoimmune thrombocytopenia

تعداد نتایج: 84689  

2017
Zakaria Hindi Nirmal Onteddu Christopher A Ching Abdallah A Khaled

INTRODUCTION Immune thrombocytopenic purpura (ITP) is an autoimmune hematological disorder that causes decreased production and destruction of platelets leading to thrombocytopenia. Although thrombocytopenia usually causes hemorrhagic problems, thrombotic events like strokes, although rare, can still occur. Management of thrombotic events in patients with ITP differs from that of patients with ...

2012
Andrew J. Lochowicz

Immune thrombocytopenia occurs when antibodies targeting specific glycoproteins (GPs) on the platelet surface lead to their destruction. Tests of the patient’s platelets and serum for antibodies and typing of DNA for human platelet alloantigens (HPA) can be helpful in confirming a clinical diagnosis of immune thrombocytopenia. A thorough workup includes 1) serum tests using intact platelets; 2)...

Journal: :Japanese journal of medicine 1990
S Yonekura T Nagao S Arimori M Miyaji K Ogoshi Y Tsutsumi

We report a case of autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura (Evans' syndrome) associated with gastric plasmacytoma. Recognition of this rare entity is important because surgery and chemotherapy together may achieve a cure. Possible mechanisms causing the hemolytic anemia and thrombocytopenia are discussed.

Journal: :Haematologica 1998
A Koşar I C Haznedaroglu Y Büyükaşik O Ozcebe S Kírazli S Dündar

Circulating thrombopoietin and interleukin-6 concentrations were investigated in two different settings of thrombocytopenia. Twenty patients with autoimmune thrombocytopenic purpura (ATP), 12 patients with aplastic anemia (AA) and 15 healthy subjects were studied. Thrombopoietin was significantly increased in AA and deficient in ATP. Interleukin-6 was significantly increased in ATP, compared to...

Journal: :P & T : a peer-reviewed journal for formulary management 2017
Ayesha M Khan Halina Mydra Ana Nevarez

Immune thrombocytopenia (ITP), previously called idiopathic thrombocytopenia purpura, is an autoimmune disorder characterized by a severe reduction in peripheral blood platelet count. In healthy individuals, normal platelet count ranges from 150-450 × 109/L, while in thrombocytopenia counts fall to less than 100 × 109/L.1 In adults, the incidence of ITP is approximately two to four per 100,000....

2012
Kan Chen

Platelets are anuclear blood cells whose function is to form blood clots when we injure ourselves, to prevent excessive blood loss. Thrombocytopenia is a relative low number of platelets in the blood. Thrombocytopenia has several possible causes, including the trapping of platelets in spleen, reduced production of platelets and increased breakdown of platelets. Some examples of an increase in p...

Journal: :International journal of life science and pharma research 2022

Immune Thrombocytopenia (ITP) is an autoimmune disorder characterised by a low platelet countless than 100? ×? 10^9/L, purpura, and hemorrhagic episodes induced antiplatelet autoantibodies without anemia or leukopenia. thrombocytopenia occurs in 2 to 4/100? 000 adults. A wide range of signs symptoms, from modest mucocutaneous petechiae severe, life-threatening organ haemorrhage, are seen ITP pa...

Journal: :Postgraduate medical journal 1987
C L Kozlowski M J Johnson D W Gorst R F Willey

This case report describes the simultaneous occurrence of autoimmune thrombocytopenia and the lupus anticoagulant in a patient with primary adenocarcinoma of the bronchus. Treatment with corticosteroids and plasmapheresis resulted in a return to normal of the partial thromboplastin time and the disappearance of the platelet antibodies. The carcinoma was inoperable.

Journal: :Blood 1978
N Gengozian C L McLaughlin

Interspecies platelet immunizations among marmosets lead to antibody formation to the donor platelets and a profound thrombocytopenia, which when associated with anemia may result in death of the animal. This actively induced immunologic thrombocytopenia closely resembles two clinical disease entities manifesting autoimmune thrombocytopenia, posttransfusion purpura and idiopathic thrombocytopen...

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