Mar 30, 2016 purpura trombocitopenica inmune inmune julian criado clinica medica heep noviembre 2015 2. What is idiopathic thrombocytopenic purpuraitp duration. A 52yearold woman with immune thrombocytopenic purpura diag nosed nine years ago has. Trombocitopenia inmune primaria pediatria integral. A mi me a ayudado a subir las plaquetas alimentos como.
Diagnosis and treatment of immune thrombocytopenic purpura wilson ruiz gil1,a. Purpura trombocitopenica autoinmune caso clinico y revision bibliografica luis angel sequeira rojas s u m m a r y the itp is a blood illness, characterize by thrombocytopenic, and it variability intense level. Thrombotic thrombocytopenic purpura description of diagnosis and management of a rare entity with a high mortality. It can produced in health people, but in children has been associated to viral infection, or bacterial infection. Thrombotic thrombocitopenic purpura is a rare disease with a morphological expression featured of many microthrombi in the terminal arterioles of several vital structures. Could appear with an all level of bleeding and sometimes involves the central nervous system cns. Trombocitopenia inmunitaria primaria alvaradoibarra m 1, aguilarandrade c1, alvarezvera jl, amadorperez ao1, anayacuellar i2, anorvehernandez e3, baezislas pe1, batesmartin.
He proposed that a powerful poison with both agglutina. Immune or idiopathic thrombocytopenic purpura itp in childhood. Purpura results from the extravasation of blood cells into the skin andor mucous membranes giving rise to small purple coloured areas that do not disappear under pressure. Abstract a 52yearold woman with immune thrombocytopenic purpura diagnosed nine years ago has presented two recurrencies relieved to immunossupressant treatment. Grading of hemorrhage in children with idiopathic thrombocytopenic purpura. Moschcowitz was the first to inform multiple hyaline thrombi as the primordial finding of a partial autopsy case. Approach to the investigation and management of immune thrombocytopenic purpura in children. Tambien puede ocurrir debido a determinados medicamentos o vacunas. The etiopathogenic mechanisms may result from abnormalities in any of the three components of hemostasis. The last one did not havea good response to corticosteroids and requireintravenous immune globulin. Autoimmmune thrombocytopenic purpura atp is a hemorrhagic disease with a more frequent presentation in infancy. Assessment of uk practice for management of acute childhood idiopathic thrombocytopenic purpura against.
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