TTP is caused by severely low ADAMTS13 activity, leading to impaired cleavage of ultralarge von Willebrand factor multimers, platelet-rich microthrombi formation, and end-organ ischemia. TTP is characterized by a relatively lower rate of renal failure and a relatively higher rate of severe thrombocytopenia and neurologic manifestations. N Engl J Med 2022; 387:e41. https://www.nejm.org/doi/full/10.1056/NEJMimc2117464
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