Anemia hemolítica microangiopática en lupus eritematoso sistémico: revisión narrativa de la literatura

a b s t r a c t Introduction: The clinical spectrum of microangiopathy disorders is vast, and needs a great clinical skill to find the origin, especially in patients with systemic lupus erythematosus, in whom it is necessary to consider: associated thrombotic thrombocytopenic purpura, antip- hospholipid syndrome, generally of the catastrophic type; localised microangiopathy, or malignant hypertension. Objective: Using the results reported in the literature, the aim of this article is to describe the frequency, causes and clinical features of thrombotic microangiopathy in systemic lupus erythematosus.