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Refractory Thrombotic Thrombocytopenic Purpura in a Patient With Triple X Syndrome
Pedro Arthur da Rocha Ribas1, Julia Ghiraldi2, Giovanna Gugelmin2
1Department of Internal Medicine, Clinical Hospital Complex of the Federal University of Paraná, Curitiba, BRA.
Abstract:
Clinical manifestations of triple X syndrome (karyotype 47, XXX) can include autoimmune diseases. We describe the occurrence of acquired thrombotic thrombocytopenic purpura (TTP), an autoimmune condition, refractory to plasmapheresis and rituximab in a patient with triple X syndrome who required vincristine administration for disease remission. To our knowledge, this rare coexistence is the first of its kind reported in Brazil.
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