Esta enfermedad afecta a varones y a mujeres por igual. Querido diario purpura trombocitopenica idiopatica pti. 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. Purpura trombotica trombocitopenica ptt the oncology. The etiopathogenic mechanisms may result from abnormalities in any of the three components of hemostasis.
Protocolo clinico e diretrizes terapeuticas portaria sasms n. We studied their clinical manifestations, type of diagnosis, as well as medical andor surgical treatment. Moschcowitz was the first to inform multiple hyaline thrombi as the primordial finding of a partial autopsy case. 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. It causes a characteristic red or purple bruiselike rash and an increased tendency to bleed. Trombocitopenia persistente parecida a purpura trombocitopenica. Pdf purpura trombocitopenica trombotica asociada a embarazo. Protocolo clinico e diretrizes terapeuticas purpura. A purpura trombocitopenica idiopatica pti, tambem conhecida como purpura trombocitopenica. It is more common in women in the third and fourth decades, posible even in postpartum. The entire sample 200 patients had idiopathic thrombocytopenic purpura as a diagnosis established, 57 % had ecchymoses, 42 %. Pdf idiopathic thrombocytopenic purpura associated with.
For more than a halfcentury after its initial recognition, mortality was near 100% and the etiology totally obscure. The diagnosis has always been difficult and the patients condition quickly worsens. Purpura trombotica trombocitopenica medicina clinica. Thrombocytopenic purpura is mostly responsible for episodes of mucocutaneous bleeding.
Idiopathic thrombocytopenic purpura itp is the most common acquired hemorrhagic alteration occurring in apparently healthy children who have suffered viral diseases, after application of common vaccines, having been medicated with drugs or received transfusions. Idade da crianca, a saude geral e o historico medico 1,2. Itp undergoes a sudden onset, with a rapid, life threatening. James, roberto stasi how i treat thrombocytopenia in preg nancy. Thrombotic thrombocitopenic purpura is a rare disease with a morphological expression featured of many microthrombi in the terminal arterioles of several vital structures. Enfermedad infantil,purpura trombocitopenica idiopatica. Thrombotic thrombocytopenic purpura ttp is the most extensive and dangerous intravascular platelet clumping disorder. Easily share your publications and get them in front of issuus. Dec 10, 20 issuu is a digital publishing platform that makes it simple to publish magazines, catalogs, newspapers, books, and more online. Our case was a 58yearold female with headache, gum bleeding, redness in legs, and ecchymoses on the arms for 10 days.
Purpura trombocitopenica, trombocitopenia, purpura trombocitopenica idiopatica, crianca. He proposed that a powerful poison with both agglutina. Purpura trombocitopenica imunologica by protocoale pediatrie. Purpura trombocitopenica idiopatica nils rodriguez abanto. The last consensus from the american society of hematology ash, published in 2011, brought some. Consenso sobre diagnostico y tratamiento 227 aronis s, platokouki h, mitsika a y col. Idiopathic thrombocytopenic purpura is included in the group of thrombocytopenics produced by immunological overdistruction. 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. Clinical laboratory could simplify the task of differencial diagnosis measuring adamts enzime. We report a case of immune thrombocytopenic purpura due to splenic tuberculosis. Immune thrombocytopenia purpura itp, also known as idiopathic thrombocytopenic purpura, is a type of thrombocytopenic purpura defined as an isolated low platelet count with a normal bone marrow in the absence of other causes of low platelets.
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