Purpura trombocitopenica hematologia pdf

Esta enfermedad afecta a varones y a mujeres por igual. It can produced in health people, but in children has been associated to viral infection, or bacterial infection. Primary immune thrombocytopenia itp is an acquired immunemediated disorder characterized by isolated low platelet count and the absence of any other cause of the thrombocytopenia. Purpura is a disease in which there is leakage of blood out of the blood vessels in the skin or mucosa, causing the presence of painless purplish spots, called petechiae small and large number stains or ecchymoses larger patches. Thrombocytopenic purpura is mostly responsible for episodes of mucocutaneous bleeding. For more than a halfcentury after its initial recognition, mortality was near 100% and the etiology totally obscure. Hematologia y oncologia pediatricas ha actualizado sus. 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. Protocolo clinico e diretrizes terapeuticas portaria sasms n. Assessment of uk practice for management of acute childhood idiopathic thrombocytopenic purpura against.

Trombocitopenia inmunitaria primaria alvaradoibarra m 1, aguilarandrade c1, alvarezvera jl, amadorperez ao1, anayacuellar i2, anorvehernandez e3, baezislas pe1, batesmartin ra 1, cervantessanchez i 1, choquecondori di, cortessanchez e, garcia camacho as1, garciafernandez l4, gomezrosas p1, grimaldogomez fa5. He proposed that a powerful poison with both agglutina. Approach to the investigation and management of immune thrombocytopenic purpura in children. Trombocitopenia inmune primaria pediatria integral. Chronic immune thrombocytopenic purpura itp is a bleeding disorder characterized by increased destruction of platelets due to the production of antiplatelet autoantibodies. Purpura are injuries caused by the extravasation of blood cells into the skin and or mucous membranes due to hemostasis disorders. Purpura trombotica trombocitopenica y sindrome hemolitico. The etiopathogenic mechanisms may result from abnormalities in any of the three components of hemostasis. Eperto e bases del diagstico e hematologa 4 purpura trombotica trombocitopenica y sindrome hemolitico uremico figura 1. Thrombotic thrombocitopenic purpura is a rare disease with a morphological expression featured of many microthrombi in the terminal arterioles of several vital structures. Purpura trombocitopenica, plaquetas, purpura, autoanticuerpos. 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. Thrombotic thrombocytopenic purpura ttp is the most extensive and dangerous intravascular platelet clumping disorder. Protocolo clinico e diretrizes terapeuticas purpura.

1048 1491 56 275 27 1309 156 1098 1014 387 108 613 1405 1137 594 1248 747 931 506 428 640 1352 1305 843 457 1522 482 1169 579 279 917 310 1550 1216 1199 667 897 59 227 1011 149 171 416