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Rinsho Ketsueki ; 51(2): 127-31, 2010 Feb.
Artículo en Japonés | MEDLINE | ID: mdl-20379104

RESUMEN

We report a patient with refractory idiopathic thrombotic thrombocytopenic purpura (TTP) who was successfully treated with rituximab. A 50-year-old woman was referred to our hospital with progressive psychoneurotic symptoms, hemolytic anemia and thrombocytopenia. The diagnosis of TTP was confirmed by the absence of ADAMTS13 activity with the presence of circulating ADAMTS13 inhibitor. High-dose steroid therapy and plasma exchange were performed. Despite 21 sessions of plasma exchange, however, there was no remarkable improvement. We then administered rituximab. Fifteen days after the first infusion of rituximab, she achieved complete remission and ADAMTS13 activity increased up to 14%. The patient has remained in remission for more than 9 months.


Asunto(s)
Anticuerpos Monoclonales/administración & dosificación , Intercambio Plasmático , Púrpura Trombocitopénica Trombótica/terapia , Proteínas ADAM/antagonistas & inhibidores , Proteínas ADAM/sangre , Proteína ADAMTS13 , Anticuerpos Monoclonales de Origen Murino , Biomarcadores/sangre , Esquema de Medicación , Femenino , Humanos , Persona de Mediana Edad , Púrpura Trombocitopénica Trombótica/diagnóstico , Inducción de Remisión , Rituximab , Resultado del Tratamiento
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