Definition, diagnosis and treatment of immune thrombocytopenic purpura
نویسندگان
چکیده
منابع مشابه
Definition, diagnosis and treatment of immune thrombocytopenic purpura.
Regulation of thrombopoiesis: effects of the degree of thrombocytopenia on megakaryocyte ploidy and platelet volume. Blood 1987;70:177-85. 29. Stenberg PE, Levin J. Ultrastructural analysis of acute immune thrombocytopenia in mice: dissociation between alterations in megakaryocytes and platelets. Cazenave J-P, et al. Intrinsic impaired proplatelet formation and microtubule coil assembly of mega...
متن کاملThrombotic Thrombocytopenic Purpura: Diagnosis and Treatment
Thrombotic Thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathic disease, associated with thrombocytopenia and hemolytic anemia. It is caused by an enzymatic dysfunction responsible in cleavage of blood clotting factors. In this study we have tried to review the available approaches in diagnoses of the disease as well as treatment strategies. Based on the what the current review ...
متن کاملClinical Features and Treatment Outcomes of 132 Infants with Immune Thrombocytopenic Purpura
Introduction: To determine common clinical symptoms, admission length, and treatment outcomes of infants with Immune Thrombocytopenic Purpura. Method: analysis of 132 infants with Immune Thrombocytopenic Purpura admitted to the emergency and hematology ward of Dr. Sheikh Hospital, with reference to age, gender, immunization history (preceding six weeks), presenting clinical features, treatment...
متن کامل[Diagnosis and treatment of idiopathic thrombocytopenic purpura].
march 2012 25 © 2012 Human Kinetics IJATT 17(2), pp. 25-28 Idiopathic thrombocytopenic purpura (ITP) is a syndrome characterized by a low platelet count in the peripheral blood that is not related to marrow failure.1 ITP is a relatively common syndrome of unknown origin that is increasingly recognized. Approximately 66 adults and 50 children per 1,000,000 are diagnosed with ITP annually.2 The...
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ژورنال
عنوان ژورنال: Haematologica
سال: 2009
ISSN: 0390-6078,1592-8721
DOI: 10.3324/haematol.2009.007674