Abstract:Thrombotic thrombocytopenic purpura (TTP) is an uncommon disorder characterized by the classic pentad of microangiopathic hemolytic anemia, thrombocytopenia, renal dysfunction, fever and neurologic abnormalities. It is associated with infections, malignancy, drugs and autoimmune diseases. TTP and systemic lupus erythematosus (SLE) rarely present simultaneously and generally constitute a diagnostic dilemma. We present a case of a 42-year-old patient with overlapping features of SLE and TTP, who was admitted to … Show more
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