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Likely causes of microangiopathic hemolytic anemia and thrombocytopenia according to presenting findings

Likely causes of microangiopathic hemolytic anemia and thrombocytopenia according to presenting findings
No clinical finding is completely sensitive or specific for a specific primary TMA diagnosis. Refer to UpToDate content on the approach to the patient with a suspected thrombotic microangiopathy for further information and an approach to the diagnostic evaluation.
TMA: thrombotic microangiopathy; MAHA: microangiopathic hemolytic anemia; DIC: disseminated intravascular coagulation; HELLP: hemolysis, elevated liver function tests, low platelets; TTP: thrombotic thrombocytopenic purpura; HUS: hemolytic-uremic syndrome.
Adapted from: George JN, Nester CM. Syndromes of thrombotic microangiopathy. N Eng J Med 2014; 371:654.
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