Purpura trombocitopenica pediatria pdf 2010

Eperto e bases del diagstico e hematologa 4 purpura trombotica trombocitopenica y sindrome hemolitico uremico figura 1. 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. Trombocitopenia inmunitaria primaria en ninos medigraphic. Psaila b, petrovic a, page lk, menell j, schonholz m, bussel jb. Which indicates that the mother and son binomial should be evaluated in an integral way. The itp working group of the spanish society of paediatric.

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. Consenso sobre diagnostico y tratamiento 227 aronis s, platokouki h, mitsika a y col. Protocol for the study and treatment of immune thrombocytopenic purpura itp. Fortysix children with henochschonlein purpura were studied. 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. Thrombotic thrombocytopenic purpura, atypical hemolytic uremic syndrome. Purpura trombotica trombocitopenica y sindrome hemolitico uremico. The incidence of immune thrombocytopenic purpura in children and adults. He proposed that a powerful poison with both agglutina. The etiopathogenic mechanisms may result from abnormalities in any of the three components of hemostasis. Purpura trombocitopenica idiopatica pti em criancas. Protocol for the study and treatment of immune thrombocytopenic purpura. Terrell d, beebe l, vesely s, neas b, segal j, george jn. We present a rare case, where there was association with pregnancy and chronic itp.

Adamts, purpura trombotica trombocitopenica, sindrome uremico hemolitico atipico. Itp 2010 abstract primary immune thrombocytopenia itp, formerly known as immune thrombocytopenic purpura, is a disease in which clinical and therapeutic management has always been controversial. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Their clinical manifestations included palpable purpura in 100%, subcutaneous edema in 30%, arthritisarthralgia in 78%, gastrointestinal involvement in 56% and renal abnormalities in 30%. Thrombocytopenic purpura is mostly responsible for episodes of mucocutaneous bleeding. Purpura trombotica trombocitopenica ptt the oncology. 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. Esta enfermedad afecta a varones y a mujeres por igual. The mother had a history of chronic idiopathic thrombocytopenic purpura itp. Moschcowitz was the first to inform multiple hyaline thrombi as the primordial finding of a partial autopsy case. Trombocitopenia inmune primaria pediatria integral. 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 inmunologica en ninos binasss.