2015, Number 3
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Residente 2015; 10 (3)
Trombocitopenia inmune primaria
García-Reyes B, Espinosa-Valdespino L, Nava-Zavala AH, Rubio-Jurado B
Language: Spanish
References: 29
Page: 154-165
PDF size: 255.10 Kb.
ABSTRACT
Primary immune thrombocytopenia is caused by excessive platelet destruction by autoantibodies directed against platelet membrane antigens as well as a deficient production by the megakaryocytes in the bone marrow. It can occur with or without bleeding. Thrombocytopenia is defined as a platelet count ‹ 100 x 10
9/L. The diagnosis is one of exclusion, in the absence of other diseases that may be associated with thrombocytopenia. The first-line of treatment are corticosteroids, but some patients do not respond to them and are candidates for second line therapy with splenectomy, rituximab or new therapies such as TPO-agonist for chronic TIP or refractory cases.
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